TIR
{

RETE|ID 1 FBti0001029	ICL 1 P	SYM 1 P{hs/runt.T}a	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 1 May 2005	RESZ 433
ID|FBti0001029
SYM|P{hs/runt.T}a
SYN|P{hs/runt}a
|hs/runt<up>a</up>
ASTP|<fbsym>FBtp0000369==P{hs/runt.T}</fbsym>
DT|1 May 2005
|15 Jul 1996
ICL|P
SK|FBst0003121
|y[1] w[67c23]; P{w[+mC]=hs/runt.T}a
|Total=1

REFDSR
{
RDID|FBrf0074646
|Tsai and Gergen
|1994
SYN|hs/runt<up>a</up>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
}

REF
{
REFM|FBrf0074646
|Tsai and Gergen
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0001115	ICL 1 P	SYM 1 P{lacW}EG	ASTR 1 -	CLOC 1 -	REF 1 1	DT 1 2 Feb 1998	RESZ 217
ID|FBti0001115
SYM|P{lacW}EG
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|2 Feb 1998
|15 Jul 1996
ICL|P
SK|FBst0001759
|Dp(1;Y)y[2]67g24.2, P{w[+mC]=lacW}EG/y[1] w[1]
|Total=1

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0001116	ICL 1 P	SYM 1 P{lacW}MG	ASTR 1 -	CLOC 1 -	REF 1 1	DT 1 2 Feb 1998	RESZ 399
ID|FBti0001116
SYM|P{lacW}MG
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|2 Feb 1998
|15 Jul 1996
ICL|P
SK|FBst0001756
|Dp(1;Y)y[2]60d19.3, P{w[+mC]=lacW}MG/y[1] w[1]
|FBst0001757
|Dp(1;Y)y[+]sc, P{w[+mC]=lacW}MG/y[1] w[1]
|FBst0001758
|Dp(1;Y)y[59b], P{w[+mC]=lacW}MG/y[1] w[1]
|FBst0007367
|Df(1)y-91g23/Dp(1;Y)y[+]sc, y[MG] P{w[+mC]=lacW}MG/FM7a
|Total=4

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002008	ICL 1 P	SYM 1 P{enF}X	ASTR 1 -	CLOC 1 3D-3E	REF 1 2	DT 1 21 Mar 1997	RESZ 297
ID|FBti0002008
SYM|P{enF}X
SYN|FX
ASTP|<fbsym>FBtp0000317==P{enF}</fbsym>
DT|21 Mar 1997
|21 Mar 1997
ICL|P

REFDSR
{
RDID|FBrf0054180
|Kassis et al.
|1991
SYN|FX
CLOC|3D-3E
|Insertion site 
LOCB|in situ
PHC|viable
}

REF
{
REFM|FBrf0054180
|Kassis et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002266	ICL 1 P	SYM 1 P{}ci<up>DRP</up>	ASTR 1 -	CLOC 1 102A1--3	REF 1 2	DT 1 4 Feb 2000	RESZ 615
ID|FBti0002266
SYM|P{}ci<up>DRP</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|P
ASGN|<fbsym>FBgn0004859==ci</fbsym>

REFDSR
{
RDID|FBrf0051821
|Orenic et al.
|1990
ASAL|<fbsym>FBal0030756==ci<up>DRP</up></fbsym>
CLOC|102A1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004859==ci</fbsym>
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ASAL|<fbsym>FBal0030756==ci<up>DRP</up></fbsym>
CLOC|102A1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004859==ci</fbsym>
}

REF
{
REFM|FBrf0051821
|Orenic et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030756==ci<up>DRP</up></fbsym>

REFDSR
{
RDID|FBrf0051821
|Orenic et al.
|1990
PHP|Homozygous embryos have a segmentation defect similar to
| <fbsym>FBal0001651==ci<up>D</up></fbsym> embryos.
PHM|embryonic epidermis
}

REF
{
REFM|FBrf0051821
|Orenic et al.
|1990
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002268	ICL 1 P	SYM 1 P{lacW}ci<up>Dplac</up>	ASTR 1 +	CLOC 1 102A1--3	REF 1 17	DT 1 29 Jul 1998	RESZ 2932
ID|FBti0002268
SYM|P{lacW}ci<up>Dplac</up>
SYN|P<up>lacW</up>ci<up>Dplac</up>
|P{lacZ-un2}ci<up>Dplac</up>
|ci-lacZ
|ci<up>D</up>-lacZ
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|29 Jul 1998
|21 Mar 1997
ICL|P
ID2|FBti0002684
ASGN|<fbsym>FBgn0004859==ci</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0001888==Ecol\lacZ<up>ci-Dplac</up>RA</fbsym>
SK|FBst0006303
|y[1] w[*]; P{w[+mC]=lacW}ci[Dplac]
|Total=1

REFDSR
{
RDID|FBrf0051822
|Eaton and Kornberg
|1990
ASAL|<fbsym>FBal0030757==ci<up>Dplac</up></fbsym>
|<fbsym>FBal0040983==Ecol\lacZ<up>ci-Dplac</up></fbsym>
CLOC|102A1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004859==ci</fbsym>
AGT|en[1]
|en[X31]
|en[59]
CVBODPC|Enhancer trap staining occurs in wide, segmentally repeated stripes in
| embryos and in imaginal discs. In both embryos and imaginal discs,
| expression was found to be in the anterior compartments and precisely
| complements <fbsym>FBgn0000577==en</fbsym> expression. In engrailed mutants, <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression
| is derepressed in the posterior compartments in embryos and imaginal discs,
| suggesting that <fbsym>FBgn0004859==ci</fbsym> expression is normally repressed by <fbsym>FBgn0000577==en</fbsym> in these cells.
CVBODP|<t> E <a>  <p> segment polarity
|<t> L <a> imaginal disc | anterior <p>
CH|enhancer trap | <fbsym>FBgn0004859==ci</fbsym>
PHC|lethal | embryonic stage | recessive
}

REFDSR
{
RDID|FBrf0055852
|Blair
|1992
CVBODPC|In pupal wing, expression in anterior compartment not uniform: slightly
| fainter in cells midway between L3 and L4 down to the AP lineage boundary.
CVBODP|transcript distribution deduced from reporter protein
|<t> L <a> dorsal mesothoracic disc | anterior compartment <p>
|<t> P <a> wing | anterior compartment <p>
}

REFDSR
{
RDID|FBrf0129701
|Alcedo et al.
|2000
SYN|ci<up>D</up>-lacZ
}

REFDSR
{
RDID|FBrf0139641
|Apidianakis et al.
|2001
SYN|ci-lacZ
|P<up>lacW</up>ci<up>Dplac</up>
}

REFDSR
{
RDID|FBrf0149689
|Jia et al.
|2002
SYN|ci-lacZ
}

REFDSR
{
RDID|FBrf0151937
|Bai and Montell
|2002
SYN|ci-lacZ
}

REFDSR
{
RDID|FBrf0180280
|Bushey and Locke
|2004
SYN|P{lacW}ci<up>Dplac</up>
ASAL|<fbsym>FBal0175735==ci<up>E1</up></fbsym>
|<fbsym>FBal0175734==ci<up>E2</up></fbsym>
}

REF
{
REFM|FBrf0051822
|Eaton and Kornberg
|1990
REFM|FBrf0055852
|Blair
|1992
REFM|FBrf0068409
|Basler and Struhl
|1994
REFM|FBrf0068581
|Locke and McDermid
|1993
REFM|FBrf0079420
|Slusarski et al.
|1995
REFM|FBrf0080306
|Pan and Rubin
|1995
REFM|FBrf0090554
|Forbes et al.
|1996
REFM|FBrf0090819
|Strutt and Mlodzik
|1996
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0093741
|Struhl et al.
|1997
REFM|FBrf0129701
|Alcedo et al.
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
REFM|FBrf0139641
|Apidianakis et al.
|2001
REFM|FBrf0149689
|Jia et al.
|2002
REFM|FBrf0151937
|Bai and Montell
|2002
REFM|FBrf0152002
|Ou et al.
|2002
REFM|FBrf0180280
|Bushey and Locke
|2004
}

ALESR
{
ASYM|<fbsym>FBal0030757==ci<up>Dplac</up></fbsym>

REFDSR
{
RDID|FBrf0051822
|Eaton and Kornberg
|1990
PHP|Semilethal over <fbsym>FBal0001657==ci<up>Ce-2</up></fbsym>, most die as embryos, adult
| survivors appear
|normal. Heterozygotes with <fbsym>FBal0001651==ci<up>D</up></fbsym> die around eclosion
| having abnormal
|legs and mouthparts.
}

REF
{
REFM|FBrf0051822
|Eaton and Kornberg
|1990
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002387	ICL 1 FB	SYM 1 FB{}w<up>DZL</up>	ASTR 1 -	CLOC 1 3B6	REF 1 7	DT 1 4 Feb 2000	RESZ 784
ID|FBti0002387
SYM|FB{}w<up>DZL</up>
ASTP|<fbsym>FBtp0011426==FB</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|FB
ASGN|<fbsym>FBgn0003996==w</fbsym>
ABA|<fbsym>FBab0024597==Dp(2;1)w<up>DZL</up></fbsym>
SK|FBst0003603
|w[DZL]
|FBst0003604
|sc[1] z[1] <fbsym>FBal0018236==w[DZL]</fbsym>
|Total=2

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
ASAL|<fbsym>FBal0018236==w<up>DZL</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0042055
|Bingham and Zachar
|1985
REFM|FBrf0051943
|Harden and Ashburner
|1990
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018236==w<up>DZL</up></fbsym>

REFDSR
{
RDID|FBrf0034850
|Bingham
|1980
PHP|Eye color: dull red brown, in <fbsym>FBgn0004050==z</fbsym><up>+</up> males.
|Eye color: yellow, in <fbsym>FBal0018822==z<up>1</up></fbsym> males and in homo- and heterozygous
|females (<fbsym>FBgn0004050==z</fbsym><up>+</up> or <fbsym>FBal0018822==z<up>1</up></fbsym>) when X's synapsed.
|Malpighian tubule color: wild-type.
|Testis color: wild-type.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0036017
|Bingham
|1981
PHP|Eye color: dull red brown, in <fbsym>FBgn0004050==z</fbsym><up>+</up> males.
|Eye color: yellow, in heterozygous or homozygous females.
|Eye color: wild-type in
| <fbsym>FBab0004254==In(1)w<up>DZL</up>-1</fbsym>/<fbsym>FBal0018236==w<up>DZL</up></fbsym>,
| <fbsym>FBab0006482==T(1;3)w<up>DZL</up></fbsym>/<fbsym>FBal0018236==w<up>DZL</up></fbsym> females.
|Eye color: wild-type in
| <fbsym>FBab0004255==In(1)w<up>DZL</up>-3</fbsym>/<fbsym>FBal0018236==w<up>DZL</up></fbsym> females.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0054158
|Rabinow et al.
|1991
PHP|Eye color: <fbsym>FBgn0004050==z</fbsym>-like.
|Shows some interaction with <fbsym>FBgn0004398==Inr-a</fbsym> mutants.
}

REF
{
REFM|FBrf0034850
|Bingham
|1980
REFM|FBrf0036017
|Bingham
|1981
REFM|FBrf0054158
|Rabinow et al.
|1991
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002388	ICL 1 copia	SYM 1 copia{}w<up>a</up>	ASTR 1 -	CLOC 1 3B6	REF 1 30	DT 1 4 Feb 2000	RESZ 10299
ID|FBti0002388
SYM|copia{}w<up>a</up>
ASTP|<fbsym>FBtp0011420==copia</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000008
|ac[4] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000053
|gt[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000082
|C(1;Y)7, y[1] v[1] bb[-]: bb[-]/Dp(1;f)1185/C(1)DX, y[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000108
|sc[6] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000121
|su(s)[2rv] <fbsym>FBal0018195==w[a]</fbsym> cv[1] t[1]
|FBst0000148
|w[a]
|FBst0000149
|w[a] mw[1] mit[1]
|FBst0000188
|y[2] sc[1] <fbsym>FBal0018195==w[a]</fbsym> ec[1]
|FBst0000189
|y[2] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000191
|In(1)m[K], y[2] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000675
|w[a]; tra[1]/TM2
|FBst0000700
|C(1;Y)1, y[1] v[1] f[1] B[1]: y[+]/C(1)RM, y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000703
|C(1;YS)1, Df(1)y-ac, <fbsym>FBal0018195==w[a]</fbsym> ct[6] f[1]/Dp(1;YL)sc[S1]/C(1)DX, y[1] f[1]
|FBst0000760
|Dp(1;f)101/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000762
|Dp(1;f)118/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000763
|Dp(1;f)107/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000764
|Dp(1;f)135, y[2]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000769
|Df(1)sc[8], sc[8] w[a]; T(1;3)sc[J4], sc[J4]
|FBst0000792
|In(1)sc[7], sc[7] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000798
|In(1)sc[8], sc[8] y[31d] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0000801
|In(1)sc[9], sc[9] <fbsym>FBal0018195==w[a]</fbsym> t[1] f[1] Bx[1]
|FBst0000849
|T(1;4)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym> B[1]/C(1)DX, y[1] f[1]
|FBst0000852
|T(1;4)w[m258-21], y[1] w[a]/FM4
|FBst0000980
|In(1)pdf, <fbsym>FBal0018195==w[a]</fbsym> pdf[1]
|FBst0001024
|Dp(2;Y)bw[+]/y[1] w[a]; E(w[a])[1]/CyO
|FBst0001156
|y[1] w[a]; Doa[3]/TM3, Ser[1]
|FBst0001260
|w[a] su(fa[swb])[1] rb[1]
|FBst0001310
|C(1;Y)6, y[2] su(w[a])[1] w[a]/0/C(1)M4, y[1]
|FBst0001392
|C(1;YS)6, In(1)EN2, oc[1] ptg[1] f[1]/R(YL)/C(1)RM, y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0001442
|In(1)sc[29], sc[29] <fbsym>FBal0018195==w[a]</fbsym> eag[sc29]
|FBst0001494
|Df(1)cho2, y[1] w[a]/FM7c
|FBst0001631
|C(1;Y)*, y[1] <fbsym>FBal0018195==w[a]</fbsym> & C(1)DX, y[1] v[1]/0
|FBst0001715
|w[a] N[fa-swb]
|FBst0002113
|gt[1] w[a]; Ki[1] pb[4] p[p] ss[a40a]/TM2
|FBst0002170
|C(1)RA60g, y[1] B[1] w[a]/FM7c/Dp(1;Y)su(f)[+]
|FBst0002211
|w[a] N[Co] rb[1]/C(1)DX, y[1] w[1] f[1]; Dp(1;2)51b/+
|FBst0002212
|w[a] N[264-40] rb[1]/C(1)DX, y[1] w[1] f[1]; Dp(1;2)72c21/+
|FBst0002324
|FM7a, In(1)nod-bd/y[1] <fbsym>FBal0018195==w[a]</fbsym> ct[6] lz[1] v[1] f[1]/Dp(1;Y)y[+]; sv[spa-pol]
|FBst0002496
|C(1;Y)8, y[1] su(w[a])[1] w[a]: y[+]; kni[ri-1] p[p] & C(1)RM, y[1] v[1] bb[1]; kni[ri-1] p[p]
|FBst0002575
|T(1;Y)N29, y[1] <fbsym>FBal0018195==w[a]</fbsym> Ste[+] f[1]: y[+] B[S]/C(1)A, y[1]
|FBst0002886
|w[a] N[fa-g]; l(2)52Fe[E6.17]/CyO
|FBst0002922
|T(1;Y)E1, y[1] <fbsym>FBal0018195==w[a]</fbsym> Ste[1]: y[+] B[S]/C(1)*, y[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003072
|w[a] N[fa-g]; l(2)52Fd[E3.27]/CyO
|FBst0003075
|w[a] N[l1N-ts2] rb[1]
|FBst0003176
|w[a] N[fa-g]; Rho1[E3.10]/CyO
|FBst0003226
|Df(1)cin-arth, In(1)sc[S1L]sc[8R], In(1)dl-49, <fbsym>FBal0018195==w[a]</fbsym> v[Of] f[1]/C(1)DX, y[1] w[1] f[1]/Dp(1;Y)y[+]
|FBst0003339
|w[a] N[fa-g]; l(2)52Fc[D8.13]/CyO
|FBst0003389
|T(1;Y)S7, y[1] <fbsym>FBal0018195==w[a]</fbsym> f[1]: y[+] B[S]/C(1)DX, y[1] w[1] f[1]
|FBst0003517
|w[a] N[fa-g]; Df(2R)Jp4/CyO
|FBst0003518
|w[a] N[fa-g]; Df(2R)Jp1/CyO
|FBst0003520
|w[a] N[fa-g]; Df(2R)Jp8, w[+]/CyO
|FBst0003521
|w[a] N[fa-g]; Df(2R)Jp6/CyO
|FBst0003522
|w[a] N[fa-g]; Df(2R)Jp7, w[+]/CyO
|FBst0003651
|Df(1)lz-90b24, y[2] w[a]/FM7c
|FBst0003652
|In(1)dvr3, y[2] <fbsym>FBal0018195==w[a]</fbsym> lz[1] dvr[92b24,2c]/FM7a
|FBst0003654
|y[2] <fbsym>FBal0018195==w[a]</fbsym> lz[1] dvr[5]/FM7a
|FBst0003655
|y[2] <fbsym>FBal0018195==w[a]</fbsym> lz[1] dvr[6]/FM7a
|FBst0003707
|y[1] <fbsym>FBal0018195==w[a]</fbsym> Ste[1]/Dp(1;Y)B[S]Yy[+]
|FBst0003752
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)129-16, y[2] y[+] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003758
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)110-8, y[2] y[+] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003759
|svr[1] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003807
|C(1)RM, y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym> bb[-]/0/C(1;Y)1, y[1] y[+]; dp[olv] wg[Sp-1] cn[1]/In(2L)Cy, S[2] Cy[1] cn[1] bw[1] sp[1]
|FBst0003838
|C(1)DX, y[1] f[1]/R(1)2, In(1)sc[8], Df(1)ac, ac[1] sc[8] <fbsym>FBal0018195==w[a]</fbsym> B[1]/Dp(1;Y)y[+]
|FBst0003934
|C(1)RM, y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym> bb[-]/R(YL)/C(1;YS)6, In(1)EN2, oc[1] ptg[1] f[1]
|FBst0003935
|Dp(1;1)Co/C(1)SB, In(1)y[4], y[4] cv[1] v[1] f[1] bb[-]: y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym> bb[-]
|FBst0003940
|Dp(1;f)1187, P{ry[+t7.2]=PZ}0801 P{ry[+t7.2]=PZ}8-23 y[+]; Df(1)sc[8], y[1] sc[8] w[a]; ry[506]
|FBst0003946
|Dp(1;f)856/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003947
|Dp(1;f)1144/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003948
|Dp(1;f)1162/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003949
|Dp(1;f)1186/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003950
|Dp(1;f)1205/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003951
|Dp(1;f)1337/Dp(1;Y)B[S]/Df(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0003952
|y[2] ph-d[br] w[a]/FM7a/Dp(1;2;Y)w[+]
|FBst0004059
|Dp(1;1)Co, y[2] w[a]/Ts(1Lt;4Lt)w[m5]; Ts(1Rt;4Rt)w[258-21]/ci[1] ey[R]
|FBst0004178
|y[1] w[a]/Dp(1;Y)w[+]y[+]
|FBst0004185
|y[2] sc[1] <fbsym>FBal0018195==w[a]</fbsym> mei-9[a]/Dp(1;Y)y[+]
|FBst0004300
|Dp(1;Y)B[S]w[+]y[+]/C(1)DX, y[1] f[1] Bx[0]/y[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0004338
|C(1)DX, y[1] f[1]/In(1)sc[S1L]sc[8R], In(1)dl-49, In(1)At, sc[8] sc[S1] <fbsym>FBal0018195==w[a]</fbsym> v[Of] At[1]
|FBst0004443
|In(1)dl-49, y[1] w[1] lz[s]/In(1)sc[L8], sc[L8] <fbsym>FBal0018195==w[a]</fbsym> m[2] car[1]
|FBst0004444
|In(1)sc[8], sc[8] <fbsym>FBal0018195==w[a]</fbsym> bb[*]
|FBst0004453
|C(1;Y)129-11, y[2] su(w[a])[1] <fbsym>FBal0018195==w[a]</fbsym>
|FBst0004494
|C(1)RM, y[1] v[1] bb[-]/C(1;Y)112-17, y[2] su(w[a])[1] w[a]/0
|FBst0004769
|y[1] <fbsym>FBal0018195==w[a]</fbsym> shakB[25]/Dp(1;Y)y[+]mal[106]/FM3
|FBst0005357
|w[a]; Df(3L)Brd12/TM3, Sb[1]
|FBst0005705
|Basc, Df(1)BA2-8, <fbsym>FBal0018195==w[a]</fbsym> B[1]/FM7c
|FBst0005779
|y[1] <fbsym>FBal0018195==w[a]</fbsym> phl[12]/FM6, w[i] dm[+]
|FBst0005952
|C(1;Y)108-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
|FBst0005953
|C(1;Y)115-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
|FBst0005966
|Df(1)64j4, y[1] <fbsym>FBal0018195==w[a]</fbsym> N[spl-1]/Dp(1;2;Y)w[+]/C(1)DX, y[1] f[1]
|FBst0005993
|Df(1)HM430, y[1] w[a]/FM6/Dp(1;Y)y[+]mal[+]
|FBst0006031
|Df(1)su(f)4B, In(1)sc[S1L]sc[8R], In(1)dl-49, y[c4] sc[8] sc[S1] <fbsym>FBal0018195==w[a]</fbsym> v[1] f[1]/l(1)14[14]/Dp(1;Y)*
|FBst0006034
|Dp(1;Y)y[+]mal[171]/w[a] f[1] su(f)[1]
|FBst0006255
|w[a] ct[6]; mei-1[1]
|FBst0006279
|Df(1)HM44, y[1] w[a]/FM7c/Dp(1;Y)y[+]mal[+]
|FBst0006348
|Df(1)sc[8], w[a]/C(1)M3, y[2]; Dp(1;3)sc[J4], y[+], jv[1]
|FBst0006349
|Df(1)sc[8], w[a]/C(1)M3, y[2]; Dp(1;3)sc[J4], y[+], mwh[1] jv[1]/TM1
|FBst0006887
|y[1] <fbsym>FBal0018195==w[a]</fbsym> l(1)3Bc[17]/FM6
|FBst0007130
|y[1] <fbsym>FBal0018195==w[a]</fbsym> mh[1]/FM7a
|FBst0008496
|y[1] <fbsym>FBal0018195==w[a]</fbsym> Dsor1[S-1221]/Basc
|FBst0008498
|y[1] <fbsym>FBal0018195==w[a]</fbsym> phl[12] hop[Tum]/Basc
|FBst0008499
|y[1] <fbsym>FBal0018195==w[a]</fbsym> phl[12] hop[T42]/Basc
|FBst0200157
|w[a]
|FBst0200678
|w[a]
|FBst1000199
|C(1)DX, y <fbsym>FBgn0003996==w</fbsym> f/ Df(1)sc[8] In(1)sc[8], w[a]/ y[+] Y
|FBst1000218
|C(1)DX, y <fbsym>FBgn0003996==w</fbsym> f/ <fbsym>FBal0018195==w[a]</fbsym> N[55e11]; Dp(1;2)51b/ +
|FBst1001483
|Y[S]X.Y[L], y[+]In(1)EN y.Y[L]y[+]/CRM, y[2] su-w[a] <fbsym>FBal0018195==w[a]</fbsym> bb/0
|FBst1001497
|ac[3] <fbsym>FBal0018195==w[a]</fbsym>
|FBst1001512
|w[a] N[55e11]/FM7, lac-z
|FBst1001732
|0/C(1;Y), y[2] su(w[a]) w[a];  ci[1] ey[R] sv[spa-pol]
|FBst1001852
|w[a] fa[g]; Df(2R)Jp1/CyO
|FBst1001853
|w[a] fa[g]; Df(2R)Jp2/CyO
|FBst1001854
|w[a] fa[g]; Df(2R)Jp4/CyO
|FBst1001855
|w[a] fa[g]; Df(2R)Jp5/CyO
|FBst1001858
|w[a] fa[g]; Df(2R)Jp8/CyO
|Total=114

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
ASAL|<fbsym>FBal0018195==w<up>a</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
PHC|viable
}

REFDSR
{
RDID|FBrf0043227
|Mount and Rubin
|1985
ASAL|<fbsym>FBal0018210==w<up>aR84e7</up></fbsym>
}

REFDSR
{
RDID|FBrf0048200
|Mount et al.
|1988
ASAL|<fbsym>FBal0018209==w<up>aR79l27</up></fbsym>
MU|spontaneous
ASAL|<fbsym>FBal0018211==w<up>aR84e19</up></fbsym>
MU|spontaneous
}

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
ASAL|<fbsym>FBal0018205==w<up>aM</up></fbsym>
MU|spontaneous
ASAL|<fbsym>FBal0018212==w<up>aR84h</up></fbsym>
MU|spontaneous
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0040134
|Goldberg et al.
|1983
REFM|FBrf0040771
|Gehring et al.
|1984
REFM|FBrf0042646
|Zachar et al.
|1985
REFM|FBrf0043227
|Mount and Rubin
|1985
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0048200
|Mount et al.
|1988
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051376
|Engels et al.
|1990
REFM|FBrf0051917
|Peng and Mount
|1990
REFM|FBrf0051943
|Harden and Ashburner
|1990
REFM|FBrf0052719
|Brierley and Flavell
|1990
REFM|FBrf0054145
|Lovering et al.
|1991
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0054964
|Kurkulos et al.
|1991
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0056235
|Hiebert and Birchler
|1992
REFM|FBrf0058549
|Sabl and Birchler
|1993
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0083249
|Lankenau
|1995
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018209==w<up>aR79l27</up></fbsym>

REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigment is restored to 80% of wild type levels.
PHM|pigment cell
}

REF
{
REFM|FBrf0043247
|Carbonare and Gehring
|1985
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0018210==w<up>aR84e7</up></fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Increased pigmentation seen in this derivative of <fbsym>FBal0018195==w<up>a</up></fbsym>
| is due to
|increased gene copy number rather than change in gene properties.
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0018212==w<up>aR84h</up></fbsym>

REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: mottled, with <fbsym>FBal0012670==mw<up>1</up></fbsym>.
}

REF
{
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0018195==w<up>a</up></fbsym>

REFDSR
{
RDID|FBrf0002371
|Muller
|1932
PHP|The amount of pigment
|formed by <fbsym>FBal0018195==w<up>a</up></fbsym> is a function of gene dose: <fbsym>FBal0018195==w<up>a</up></fbsym>/-
|female < <fbsym>FBal0018195==w<up>a</up></fbsym>/Y male = <fbsym>FBal0018195==w<up>a</up></fbsym>/<fbsym>FBal0018195==w<up>a</up></fbsym>
|female <
| <fbsym>FBal0018195==w<up>a</up></fbsym>/<fbsym>FBal0018195==w<up>a</up></fbsym>/<fbsym>FBal0018195==w<up>a</up></fbsym>
| female < <fbsym>FBal0018195==w<up>a</up></fbsym>/<fbsym>FBal0018195==w<up>a</up></fbsym> male.
}

REFDSR
{
RDID|FBrf0003530
|Beadle and Ephrussi
|1936
PHP|A <fbsym>FBal0018195==w<up>a</up></fbsym> optic disk transplanted into a
|wild-type host shows autonomous eye color development.
}

REFDSR
{
RDID|FBrf0022720
|Gelbart
|1971
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: orange-brown.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0040490
|Levis et al.
|1984
PHP|Eye color: slightly darker than <fbsym>FBal0018195==w<up>a</up></fbsym> in the triple
| mutant <fbsym>FBgn0003638==su(w<up>a</up>)</fbsym>
|<fbsym>FBal0018195==w<up>a</up></fbsym> <fbsym>FBal0016266==su(f)<up>1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0047022
|Pastink et al.
|1987
PHP|Eye color: <fbsym>FBal0018302==w<up>sp1</up></fbsym>/<fbsym>FBal0018195==w<up>a</up></fbsym> flies
| have brown eyes at eclosion, which
|become somewhat darker with age.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
PHP|Enhanced by duplications of <fbsym>FBgn0000480==Doa</fbsym><up>+</up>.
PHM|pigment cell
|ocellus
|testis
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0049880
|Birchler and Hiebert
|1989
PHP|Strong response to E(w<up>a</up>).
}

REFDSR
{
RDID|FBrf0051376
|Engels et al.
|1990
PHP|Eye color: orange.
PHM|pigment cell & adult
}

REFDSR
{
RDID|FBrf0055430
|Montell et al.
|1992
PHP|Eye color: orange.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
PHP|Homozygous males are darker than homozygous females. Triple X metafemale
|individuals homozygous for <fbsym>FBal0018195==w<up>a</up></fbsym> exhibit dosage
| compensation of pigment
|levels.
}

REFDSR
{
RDID|FBrf0056235
|Hiebert and Birchler
|1992
PHP|Eye color: yellow-orange.
|<fbsym>FBal0018195==w<up>a</up></fbsym> is slightly dosage overcompensated in males conferring
|slightly more eye pigment.
}

REFDSR
{
RDID|FBrf0073338
|Hiebert and Birchler
|1994
PHP|<fbsym>FBal0012337==mle<up>4</up></fbsym> has very little effect on the dosage
| compensation of <fbsym>FBal0018195==w<up>a</up></fbsym>:
|homozygous males have slightly darker eyes than their heterozygous
|brothers.
}

REFDSR
{
RDID|FBrf0080045
|Georgiev
|1994
PHP|Modified by <fbsym>FBgn0004050==z</fbsym> mutations.
}

REFDSR
{
RDID|FBrf0080335
|Qian and Pirrotta
|1995
PHP|Shows slight hyper dosage compensation.
}

REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: white in <fbsym>FBal0018195==w<up>a</up></fbsym> <fbsym>FBal0018224==w<up>ch</up></fbsym>.
|Eye color: white in <fbsym>FBal0018215==w<up>bf</up></fbsym> <fbsym>FBal0018195==w<up>a</up></fbsym>.
|Eye color: like <fbsym>FBal0018195==w<up>a</up></fbsym> in <fbsym>FBal0018220==w<up>Bwx</up></fbsym> <fbsym>FBal0018195==w<up>a</up></fbsym>.
|Eye color: yellowish with orange tone in males; lighter and somewhat
|yellower in females.
|Eye color: mottled, with <fbsym>FBal0012670==mw<up>1</up></fbsym>.
|Eye color: nearly white with <fbsym>FBal0014434==rb<up>1</up></fbsym>.
|Eye color: nearly white with <fbsym>FBal0004957==g<up>1</up></fbsym>.
|Malpighian tubule color: colorless.
|Eye color: mottled, with <fbsym>FBal0012670==mw<up>1</up></fbsym>.
PHM|pigment cell
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0105774
|Benevolenskaya et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0128132
|Benevolenskaya et al.
|2000
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have dull orange eyes with only 3% red pigment (compared
|to 100% pigment in wild type).
PHM|pigment cell
}

REF
{
REFM|FBrf0002371
|Muller
|1932
REFM|FBrf0003530
|Beadle and Ephrussi
|1936
REFM|FBrf0022720
|Gelbart
|1971
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0040490
|Levis et al.
|1984
REFM|FBrf0047022
|Pastink et al.
|1987
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0049880
|Birchler and Hiebert
|1989
REFM|FBrf0051376
|Engels et al.
|1990
REFM|FBrf0055430
|Montell et al.
|1992
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0056235
|Hiebert and Birchler
|1992
REFM|FBrf0073338
|Hiebert and Birchler
|1994
REFM|FBrf0080045
|Georgiev
|1994
REFM|FBrf0080335
|Qian and Pirrotta
|1995
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105774
|Benevolenskaya et al.
|1998
REFM|FBrf0128132
|Benevolenskaya et al.
|2000
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0018205==w<up>aM</up></fbsym>

REFDSR
{
RDID|FBrf0012636
|Green
|1959
PHP|Intermediate between <fbsym>FBal0018195==w<up>a</up></fbsym> and wild-type in phenotype.
}

REFDSR
{
RDID|FBrf0043247
|Carbonare and Gehring
|1985
PHP|Eye pigmentation is restored to 80% of wild type levels.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: darker than <fbsym>FBal0018195==w<up>a</up></fbsym>, with more brown pigment.
|Eye color: mottled, with <fbsym>FBal0012670==mw<up>1</up></fbsym>.
PHM|pigment cell
}

REF
{
REFM|FBrf0012636
|Green
|1959
REFM|FBrf0043247
|Carbonare and Gehring
|1985
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002389	ICL 1 roo	SYM 1 roo{}w<up>bf</up>	ASTR 1 -	CLOC 1 3B6	REF 1 13	DT 1 4 Feb 2000	RESZ 999
ID|FBti0002389
SYM|roo{}w<up>bf</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|roo
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000157
|w[bf] f[5]
|FBst0000681
|y[2] z[ae(bx)2] w[bf]/C(1)M3, y[2]; Sb[sbd-2] ss[1] Ubx[bx-34e]/TM1
|Total=2

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
ASAL|<fbsym>FBal0018215==w<up>bf</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0080401
|Soriano et al.
|1995
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018215==w<up>bf</up></fbsym>

REFDSR
{
RDID|FBrf0012683
|Green
|1959
PHP|Eye color: lighter than either mutation alone, with <fbsym>FBal0004957==g<up>1</up></fbsym>.
|Eye color: lighter than either mutation alone, with <fbsym>FBal0014434==rb<up>1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0063825
|Redfield
|1952
PHP|Spontaneously reverts.
|Eye color: light buff; somewhat lighter in males; lighter at 19<up>o</up>C
| than at 25<up>o</up>C.
|Malpighian tubule color: colorless.
PHM|pigment cell
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have faint yellow eyes with only 2% red pigment (compared
|to 100% pigment in wild type).
PHM|pigment cell
}

REF
{
REFM|FBrf0012683
|Green
|1959
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0063825
|Redfield
|1952
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002392	ICL 1 roo	SYM 1 roo{}Antp<up>Ns</up>	ASTR 1 -	CLOC 1 84A6--B2	REF 1 3	DT 1 4 Feb 2000	RESZ 588
ID|FBti0002392
SYM|roo{}Antp<up>Ns</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|roo
ASGN|<fbsym>FBgn0000095==Antp</fbsym>
SK|FBst0002235
|Antp[Ns]
|Total=1

REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|<fbsym>FBal0000587==Antp<up>Ns</up></fbsym>
MU|spontaneous
CLOC|84A6--B2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000095==Antp</fbsym>
PHC|viable
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}

REF
{
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0046285
|Jorgensen and Garber
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0000587==Antp<up>Ns</up></fbsym>

REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHP|Antenna are leg-like.
PHM|antenna
}

REFDSR
{
RDID|FBrf0034853
|Lewis et al.
|1980
PHP|Transformation of antenna to prothoracic leg identity.
PHM|antenna
}

REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Antennae to leg transformation.
PHM|antenna
}

REFDSR
{
RDID|FBrf0046285
|Jorgensen and Garber
|1987
PHP|Transformation of head to thoracic tissue.
}

REFDSR
{
RDID|FBrf0050866
|McKenna et al.
|1989
PHP|Partial transformation of antennae into legs. Flies exhibit diminished
|chemosensory jump behavior to ethyl acetate but no change in the jump
|response to a visual stimulus.
PHM|antenna
}

REFDSR
{
RDID|FBrf0055569
|Tamkun et al.
|1992
PHP|<fbsym>FBal0000587==Antp<up>Ns</up></fbsym> derepresses the <fbsym>FBgn0000095==Antp</fbsym> P2 promoter in the
| eye-antennal disc.
|The penetrance of antennae to leg transformations of
| <fbsym>FBal0000587==Antp<up>Ns</up></fbsym> mutations
|is greatly reduced in <fbsym>FBal0001295==brm<up>1</up></fbsym> heterozygotes.
PHM|antenna
}

REFDSR
{
RDID|FBrf0079983
|Denell
|1994
PHP|A viable dominant leg to antenna transformation.
PHM|antenna
}

REFDSR
{
RDID|FBrf0090426
|Adamson and Shearn
|1996
PHM|antenna
}

REFDSR
{
RDID|FBrf0094223
|Brizuela and Kennison
|1997
PHP|96-99% of heterozygotes show differentiation of leg structures in the
|antennae.
PHM|antenna
}

REFDSR
{
RDID|FBrf0098938
|Bhojwani et al.
|1997
PHP|Antenna to leg transformation.
|Heterozygotes exhibit reduced compound eye and ommatidia are replaced
|by micro- and macrochaetae.
PHM|antenna
|ommatidium
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|In extreme cases, <fbsym>FBal0000587==Antp<up>Ns</up></fbsym>/+ forms, in place of an
| antenna, a
|complete leg that includes sternopleura, coxa, trochanter, femur,
|tibia, and tarsus. Antennal leg has no sex comb in male, and
|bristle pattern is that of a middle leg. Eyes smaller; whole
|head tends to be malformed. <fbsym>FBal0000587==Antp<up>Ns</up></fbsym> <fbsym>FBal0016092==ss<up>a</up></fbsym>/+
|<fbsym>FBal0016092==ss<up>a</up></fbsym> indistinguishable from <fbsym>FBal0000587==Antp<up>Ns</up></fbsym>/+.
|<fbsym>FBal0000587==Antp<up>Ns</up></fbsym>/<fbsym>FBal0000580==Antp<up>B</up></fbsym>
|... (see <fbsym>FBal0000587==Antp<up>Ns</up></fbsym> report)
PHM|antenna
|eye
|head
}

REFDSR
{
RDID|FBrf0107412
|Vazquez et al.
|1999
PHP|96% of heterozygous flies show transformation of antenna to leg.
PHM|antenna
|leg | ectopic
}

REFDSR
{
RDID|FBrf0155665
|Zraly et al.
|2003
PHP|Heterozygotes show transformation of antenna to leg.
PHM|antenna
|leg | ectopic
}

REFDSR
{
RDID|FBrf0155711
|Gutierrez et al.
|2003
PHP|95% of mutant flies show an antenna to leg transformation.
PHM|antenna
|leg | ectopic
}

REFDSR
{
RDID|FBrf0180288
|Kankel et al.
|2004
PHP|Only 15% of heterozygotes show normal arista development.
PHM|arista
}

REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034853
|Lewis et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0046285
|Jorgensen and Garber
|1987
REFM|FBrf0050866
|McKenna et al.
|1989
REFM|FBrf0055569
|Tamkun et al.
|1992
REFM|FBrf0079983
|Denell
|1994
REFM|FBrf0090426
|Adamson and Shearn
|1996
REFM|FBrf0094223
|Brizuela and Kennison
|1997
REFM|FBrf0098938
|Bhojwani et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107412
|Vazquez et al.
|1999
REFM|FBrf0155665
|Zraly et al.
|2003
REFM|FBrf0155711
|Gutierrez et al.
|2003
REFM|FBrf0180288
|Kankel et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002416	ICL 1 copia	SYM 1 copia{}sc<up>Hw-Ua</up>	ASTR 1 -	CLOC 1 1A8	REF 1 4	DT 1 4 Feb 2000	RESZ 506
ID|FBti0002416
SYM|copia{}sc<up>Hw-Ua</up>
ASTP|<fbsym>FBtp0011420==copia</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|copia
ASGN|<fbsym>FBgn0004170==sc</fbsym>

REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
ASAL|<fbsym>FBal0015253==sc<up>Hw-Ua</up></fbsym>
CLOC|1A8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004170==sc</fbsym>
}

REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0015253==sc<up>Hw-Ua</up></fbsym>

REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
PHP|Differentiation of extra chaetes on the cuticle.
}

REFDSR
{
RDID|FBrf0045360
|Garcia Alonso and Garcia-Bellido
|1986
PHP|Weak <fbsym>FBal0000167==ac<up>Hw-1</up></fbsym> phenotype in heterozygous females.
| Phenotype only slightly
|enhanced by suppressing the pre-existing <fbsym>FBal0015189==sc<up>1</up></fbsym> allele with
|<fbsym>FBal0016319==su(Hw)<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|See a partial suppression of the sc phenotype. Mutations in su(f),
|E(w<up>a</up>) and mw had no effect on the phenotype.
}

REFDSR
{
RDID|FBrf0058584
|Rabinow et al.
|1993
PHP|<fbsym>FBgn0000480==Doa</fbsym> mutants cause suppression of <fbsym>FBal0015253==sc<up>Hw-Ua</up></fbsym> and
| result in loss of
|scutellar bristles.
}

REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0045360
|Garcia Alonso and Garcia-Bellido
|1986
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0058584
|Rabinow et al.
|1993
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002417	ICL 1 gypsy{BS	SYM 1 gypsy{BS{}BS{}}ac<up>Hw-BS</up>	ASTR 1 -	CLOC 1 1A6	REF 1 4	DT 1 3 Mar 2004	RESZ 1146
ID|FBti0002417
SYM|gypsy{BS{}BS{}}ac<up>Hw-BS</up>
SYN|BS{}BS{}ac<up>Hw-BS</up>
|BS{}ac<up>Hw-BS</up>
|gypsy{BS{}}ac<up>Hw-BS</up>
|gypsy{}ac<up>Hw-1</up>
ASTP|<fbsym>FBtp0017776==gypsy{BS{}BS{}}</fbsym>
DT|3 Mar 2004
|21 Mar 1997
ICL|gypsy{BS
PRG|<fbsym>FBti0002418==gypsy{}ac<up>Hw-1</up></fbsym>
ASGN|<fbsym>FBgn0000022==ac</fbsym>

REFDSR
{
RDID|FBrf0043905
|Campuzano et al.
|1986
CLOC|1A6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000022==ac</fbsym>
CC|Additional insertion:
}

REFDSR
{
RDID|FBrf0082729
|Udomkit et al.
|1995
ASAL|<fbsym>FBal0000178==ac<up>Hw-BS</up></fbsym>
MU|spontaneous
CC|Additional insertion(s): insertion of two <fbsym>FBgn0000224==BS</fbsym> elements within the <fbsym>FBgn0001167==gypsy</fbsym>
| element in the progenitor chromosome,  <fbsym>FBti0002418==gypsy{}ac<up>Hw-1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|Insertion of 2 <fbsym>FBgn0000224==BS</fbsym> elements into <fbsym>FBgn0001167==gypsy</fbsym> element.
}

REF
{
REFM|FBrf0043905
|Campuzano et al.
|1986
REFM|FBrf0049522
|Harrison et al.
|1989
REFM|FBrf0082729
|Udomkit et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0000178==ac<up>Hw-BS</up></fbsym>

REFDSR
{
RDID|FBrf0049522
|Harrison et al.
|1989
PHP|Partial revertant.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Slightly weaker phenotype than <fbsym>FBal0000167==ac<up>Hw-1</up></fbsym>.
PHM|macrochaeta & head
|macrochaeta & thorax
|sensillum campaniformium
|microchaeta
}

REF
{
REFM|FBrf0049522
|Harrison et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002427	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bx-AV</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 4 Feb 2000	RESZ 443
ID|FBti0002427
SYM|gypsy{}Ubx<up>bx-AV</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0044226
|Peifer and Bender
|1986
ASAL|<fbsym>FBal0017525==Ubx<up>bx-AV</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0044226
|Peifer and Bender
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0017525==Ubx<up>bx-AV</up></fbsym>

REFDSR
{
RDID|FBrf0044226
|Peifer and Bender
|1986
PHP|Haltere are transformed to wing and are 15% of wing size, dorsal tissue of
|T3 is incompletely transformed to metanotum, hypopleural plates are
|incompletely transformed to sternopleural plates, 8-9 hypopleural bristles
|are still present and the anterior third leg displays a strong transformation
|to anterior second leg, as seen by the bristle pattern.  Phenotype can be
|suppressed by <fbsym>FBgn0003567==su(Hw)</fbsym> mutations.
PHM|haltere
|metathoracic segment | dorsal
|katepimeron
|metathoracic leg | anterior
}

REF
{
REFM|FBrf0044226
|Peifer and Bender
|1986
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002428	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bx-G</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 3	DT 1 4 Feb 2000	RESZ 479
ID|FBti0002428
SYM|gypsy{}Ubx<up>bx-G</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0044226
|Peifer and Bender
|1986
ASAL|<fbsym>FBal0017527==Ubx<up>bx-G</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0044226
|Peifer and Bender
|1986
REFM|FBrf0051987
|Little et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0017527==Ubx<up>bx-G</up></fbsym>

REFDSR
{
RDID|FBrf0044226
|Peifer and Bender
|1986
PHP|Haltere are transformed to wing and are 5-7.5% of wing size, dorsal tissue
|of T3 is incompletely transformed to metanotum, hypopleural plates are
|incompletely transformed to sternopleural plates, 3-5 hypopleural bristles
|are still present and the anterior third leg displays a strong transformation
|to anterior second leg, as seen by the bristle pattern.  Phenotype can be
|suppressed by <fbsym>FBgn0003567==su(Hw)</fbsym> mutation.
PHM|haltere
|metathoracic segment | dorsal
|katepimeron
|metathoracic leg | anterior
}

REF
{
REFM|FBrf0044226
|Peifer and Bender
|1986
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002445	ICL 1 H	SYM 1 H{}dpp<up>d-blk</up>	ASTR 1 -	CLOC 1 22F1--3	REF 1 2	DT 1 4 Feb 2000	RESZ 490
ID|FBti0002445
SYM|H{}dpp<up>d-blk</up>
ASTP|<fbsym>FBtp0011431==hobo</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|H
PRG|H{}OR<up>S</up>22F1,2
ASGN|<fbsym>FBgn0000490==dpp</fbsym>

REFDSR
{
RDID|FBrf0045767
|Blackman et al.
|1987
ASAL|<fbsym>FBal0002996==dpp<up>d-blk</up></fbsym>
|<fbsym>FBal0031066==dpp<up>hb1</up></fbsym>
CLOC|22F1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000490==dpp</fbsym>
}

REF
{
REFM|FBrf0045767
|Blackman et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002996==dpp<up>d-blk</up></fbsym>

REFDSR
{
RDID|FBrf0045767
|Blackman et al.
|1987
PHP|Eye reduced in size.
PHM|eye
}

REFDSR
{
RDID|FBrf0051842
|Masucci et al.
|1990
PHP|Reduction in number of eye facets. Mutant phenotype can be rescued
|by <fbsym>FBtp0004773==P{TnJMB7}</fbsym>.
PHM|ommatidium
}

REFDSR
{
RDID|FBrf0053657
|Eissenberg and Ryerse
|1991
PHP|Transheterozygotes with <fbsym>FBal0051586==ey-2<up>unspecified</up></fbsym> are normal.
}

REFDSR
{
RDID|FBrf0074522
|Staehling-Hampton et al.
|1994
PHP|Small eye phenotype.
PHM|ommatidium
}

REFDSR
{
RDID|FBrf0084454
|Treisman and Rubin
|1995
PHP|Allows furrow movement only in the central region of the eye disc,
|loss of one copy of <fbsym>FBgn0004009==wg</fbsym> is sufficient to increase the size of the
|eye.
PHM|morphogenetic furrow
}

REFDSR
{
RDID|FBrf0089199
|Wiersdorff et al.
|1996
PHP|Eye discs have a similar appearance to those of hypomorphic <fbsym>FBgn0011648==Mad</fbsym> alleles.
|The furrow initiates in a restricted area at the posterior edge and
|<fbsym>FBgn0000490==dpp</fbsym> expression is not maintained along the posterior margin.
PHM|eye-antennal disc
|morphogenetic furrow
}

REFDSR
{
RDID|FBrf0094416
|Chanut and Heberlein
|1997
PHP|Ommatidial array is slightly disorganized but an equator is still discernible
|separating 10 or more rows of dorsal ommatidia from 2-3 rows of ventral
|ommatidia. Head cuticle replaces portions of the retinal field near
|the dorsal and ventral margins (the effect is more pronounced ventrally).
|Rotational polarity is maintained in dorsal and ventral portions.
|Asymmetric retinal differentiation occurs with retinal development
|(failure of ommatidial differentiation in the ventral eye disc), it
|... (see <fbsym>FBal0002996==dpp<up>d-blk</up></fbsym> report)
PHM|ommatidium
|retina
}

REFDSR
{
RDID|FBrf0096472
|Treisman et al.
|1997
PHP|Small eye phenotype.
PHM|eye
}

REFDSR
{
RDID|FBrf0099288
|Jackson et al.
|1997
PHP|<fbsym>FBal0009563==dally<up>06464</up></fbsym> homozygotes show a slight reduction in
| the eye which
|is more severe when they are also heterozygous for <fbsym>FBal0002996==dpp<up>d-blk</up></fbsym>.
}

REFDSR
{
RDID|FBrf0099885
|Royet and Finkelstein
|1997
PHP|Homozygotes have greatly reduced compound eyes consisting of only a
|few ommatidia. The eye is largely replaced by frons cuticle, with
|ectopic frons cuticle lying between the orbital cuticle and the remaining
|ommatidia, and also between the shingle cuticle and ommatidia.
PHM|eye
|ommatidium
|frons | ectopic
}

REFDSR
{
RDID|FBrf0105843
|Horsfield et al.
|1998
PHP|Small, rough eyes.
PHM|eye
}

REFDSR
{
RDID|FBrf0125176
|Curtiss and Mlodzik
|2000
PHP|A morphogenetic furrow initiates only in the center of mutant eye discs.
|Although it progresses anteriorly in a normal fashion, it fails to
|spread laterally. Homozygous flies have small eyes.
PHM|morphogenetic furrow
|eye
}

REFDSR
{
RDID|FBrf0160742
|Lin et al.
|2003
PHP|Mutant show partial inhibition of the morphogenetic furrow, and reduced
|photoreceptor differentiation, resulting in a small eye phenotype in
|adults.
PHM|morphogenetic furrow
|eye
|photoreceptor cell
}

REFDSR
{
RDID|FBrf0167623
|Bach et al.
|2003
PHP|Homozygotes have small eyes.
PHM|eye
}

REFDSR
{
RDID|FBrf0173071
|Sedkov et al.
|2003
PHM|eye
}

REF
{
REFM|FBrf0045767
|Blackman et al.
|1987
REFM|FBrf0051842
|Masucci et al.
|1990
REFM|FBrf0053657
|Eissenberg and Ryerse
|1991
REFM|FBrf0074522
|Staehling-Hampton et al.
|1994
REFM|FBrf0084454
|Treisman and Rubin
|1995
REFM|FBrf0089199
|Wiersdorff et al.
|1996
REFM|FBrf0094416
|Chanut and Heberlein
|1997
REFM|FBrf0096472
|Treisman et al.
|1997
REFM|FBrf0099288
|Jackson et al.
|1997
REFM|FBrf0099885
|Royet and Finkelstein
|1997
REFM|FBrf0105843
|Horsfield et al.
|1998
REFM|FBrf0125176
|Curtiss and Mlodzik
|2000
REFM|FBrf0160742
|Lin et al.
|2003
REFM|FBrf0167623
|Bach et al.
|2003
REFM|FBrf0173071
|Sedkov et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002615	ICL 1 P	SYM 1 P{lacW}pros<up>W</up>	ASTR 1 -	CLOC 1 86E2--4	REF 1 3	DT 1 21 Mar 1997	RESZ 801
ID|FBti0002615
SYM|P{lacW}pros<up>W</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|21 Mar 1997
|21 Mar 1997
ICL|P
ASGN|<fbsym>FBgn0004595==pros</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0053403
|Vaessin et al.
|1991
ASAL|<fbsym>FBal0041852==Ecol\lacZ<up>pros-W</up></fbsym>
|<fbsym>FBal0039823==pros<up>W</up></fbsym>
CLOC|86E2--4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004595==pros</fbsym>
CH|enhancer trap |   | neural
PHC|lethal | recessive
CC|Expressed in neuronal precursor cells.
}

REFDSR
{
RDID|FBrf0058082
|Dawson et al.
|1993
CH|enhancer trap |   | neural
CC|Used as cell-specific marker for neurons and associated support cells.
}

REF
{
REFM|FBrf0053403
|Vaessin et al.
|1991
REFM|FBrf0058082
|Dawson et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002631	ICL 1 Tirant	SYM 1 Tirant{}Ser<up>D</up>	ASTR 1 -	CLOC 1 97E6--8	REF 1 4	DT 1 4 Feb 2000	RESZ 502
ID|FBti0002631
SYM|Tirant{}Ser<up>D</up>
ASTP|<fbsym>FBtp0011467==Tirant</fbsym>
DT|4 Feb 2000
|21 Mar 1997
ICL|Tirant
ASGN|<fbsym>FBgn0004197==Ser</fbsym>

REFDSR
{
RDID|FBrf0079512
|Thomas et al.
|1995
ASAL|<fbsym>FBal0030220==Ser<up>D</up></fbsym>
CLOC|97E6--8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004197==Ser</fbsym>
}

REF
{
REFM|FBrf0079512
|Thomas et al.
|1995
REFM|FBrf0091127
|Murata et al.
|1996
REFM|FBrf0092564
|Hukriede and Fleming
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030220==Ser<up>D</up></fbsym>

REFDSR
{
RDID|FBrf0051848
|Fleming et al.
|1990
PHP|Heterozygotes have wing notches in the adult: dominant wing-nicking
|phenotype. <fbsym>FBal0030220==Ser<up>D</up></fbsym>/<fbsym>FBal0012890==N<up>nd-1</up></fbsym>
| transheterozygotes display a synergistic phenotype:
|loss of anterior and posterior wing margins and loss of distal wing
|blade tissue. <fbsym>FBal0030220==Ser<up>D</up></fbsym>/<fbsym>FBab0003125==Dp(1;2)51bV76e</fbsym>
| flies have wild type wings.
}

REFDSR
{
RDID|FBrf0053814
|Thomas et al.
|1991
PHP|Hemizygotes and homozygotes are viable. Notches on wing tip between
|the third and fifth vein. Penetrance and expressivity of phenotype
|in heterzygotes is slightly affected by temperature: fully penetrant
|at 18<up>o</up>C and weaker at 28<up>o</up>C.
}

REFDSR
{
RDID|FBrf0079512
|Thomas et al.
|1995
PHP|Homozygotes and heterozygotes exhibit scalloping of the wing margin
|due to cell death during pupal stages.
PHM|wing
}

REFDSR
{
RDID|FBrf0091127
|Murata et al.
|1996
PHP|Heterozygotes show notching of the wing, in particular in between the
|second and fifth wing veins.
PHM|wing
}

REFDSR
{
RDID|FBrf0092564
|Hukriede and Fleming
|1997
PHP|Heterozygotes exhibit loss of distal wing margin material, phenotype
|is enhanced in homozygotes.
| <fbsym>FBal0015418==Ser<up>Bd-3</up></fbsym>/<fbsym>FBal0030220==Ser<up>D</up></fbsym> transheterozygotes
|exhibit loss of distal wing margin material, similar to
| <fbsym>FBal0030220==Ser<up>D</up></fbsym> heterozygotes.
PHM|wing | distal
}

REFDSR
{
RDID|FBrf0099884
|Sotillos et al.
|1997
PHM|wing
}

REFDSR
{
RDID|FBrf0127327
|Shyamala and Chopra
|1999
PHP|Heterozygotes show slight scalloping of the wing blade along the tip
|and towards the posterior margin.
PHM|wing
}

REFDSR
{
RDID|FBrf0151813
|Tsuda et al.
|2002
PHM|wing
}

REF
{
REFM|FBrf0051848
|Fleming et al.
|1990
REFM|FBrf0053814
|Thomas et al.
|1991
REFM|FBrf0079512
|Thomas et al.
|1995
REFM|FBrf0091127
|Murata et al.
|1996
REFM|FBrf0092564
|Hukriede and Fleming
|1997
REFM|FBrf0099884
|Sotillos et al.
|1997
REFM|FBrf0127327
|Shyamala and Chopra
|1999
REFM|FBrf0151813
|Tsuda et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002825	ICL 1 ?	SYM 1 ?{}Antp<up>Scx</up>	ASTR 1 -	CLOC 1 84A6--B2	REF 1 5	DT 1 5 Feb 1999	RESZ 1379
ID|FBti0002825
SYM|?{}Antp<up>Scx</up>
DT|5 Feb 1999
|24 Jun 1997
ICL|?
ASGN|<fbsym>FBgn0000095==Antp</fbsym>
|<fbsym>FBgn0003339==Scr</fbsym>
SK|FBst0002250
|ru[1] h[1] st[1] kni[ri-1] <fbsym>FBal0000617==Antp[Scx]</fbsym> p[p] e[s]/TM3, Sb[1]
|FBst0002257
|Antp[Scx] p[p] Sb[sbd-2] Ubx[bx-3] Ubx[pbx-1]/TM3, Sb[1]
|FBst0003407
|ru[1] h[1] st[1] cp[1] in[1] kni[ri-1] <fbsym>FBal0000617==Antp[Scx]</fbsym> p[p] cu[1] e[1]/TM3, Sb[1]
|Total=3

REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
ASAL|<fbsym>FBal0000617==Antp<up>Scx</up></fbsym>
MU|spontaneous
CLOC|84A6--B2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000095==Antp</fbsym>
PHC|lethal | recessive
CC|Insertion determined to be repetitive; approximately 3kb; not shown to
| coorelate with mutant phenotype.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
ASAL|<fbsym>FBal0138396==Scr<up>Scx</up></fbsym>
PHC|(with Antp<up>1</up>) lethal
|(with Antp<up>23</up>) lethal
}

REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149025
|Southworth and Kennison
|2002
}

ALESR
{
ASYM|<fbsym>FBal0138396==Scr<up>Scx</up></fbsym>

REFDSR
{
RDID|FBrf0149025
|Southworth and Kennison
|2002
PHP|Heterozygous males have an average of 2.7 ectopic sex comb teeth per
|second leg. The number of sex comb teeth on the first leg is normal.
|<fbsym>FBal0138396==Scr<up>Scx</up></fbsym>/<fbsym>FBal0015280==Scr<up>4</up></fbsym> males have the
| same average number of sex comb
|teeth per first leg as <fbsym>FBal0015280==Scr<up>4</up></fbsym>/+ males.
|Heterozygous males have an average of 0.1 ectopic sex comb teeth per
|third leg.
|<fbsym>FBal0138396==Scr<up>Scx</up></fbsym>/<fbsym>FBal0015278==Scr<up>2</up></fbsym> males have an
| average of 1.3 ectopic sex comb teeth
|... (see <fbsym>FBal0138396==Scr<up>Scx</up></fbsym> report)
PHM|mesothoracic leg & sex comb | ectopic
|metathoracic leg & sex comb | ectopic
|(with Scr<up>2</up>) mesothoracic leg & sex comb | ectopic
|(with Scr<up>4</up>) mesothoracic leg & sex comb | ectopic
|(with Scr<up>4</up>) metathoracic leg & sex comb | ectopic
|(with Scr<up>4</up>, Dp(3;Y)77ab) mesothoracic leg & sex comb | ectopic
|(with Scr<up>4</up>, Dp(3;Y)77ab) metathoracic leg & sex comb | ectopic
|(with Scr<up>Tpl9</up>) mesothoracic leg & sex comb | ectopic
|(with Scr<up>Tpl9</up>) metathoracic leg & sex comb | ectopic
}

REF
{
REFM|FBrf0149025
|Southworth and Kennison
|2002
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0000617==Antp<up>Scx</up></fbsym>

REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHP|Sex combs are present on all male legs.
PHM|sex comb | ectopic
}

REFDSR
{
RDID|FBrf0034841
|Kaufman et al.
|1980
PHP|Sex comb teeth are produced on the basitarsus of all six legs (transformation
|of meso- and metathoracic into prothoracic legs).
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}

REFDSR
{
RDID|FBrf0034853
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic legs to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}

REFDSR
{
RDID|FBrf0039012
|Scott et al.
|1983
PHP|Partial transformation of second and third legs into first legs.
PHM|mesothoracic leg
|metathoracic leg
}

REFDSR
{
RDID|FBrf0043249
|Dura et al.
|1985
PHP|Enhanced by <fbsym>FBal0013723==ph-d<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0046404
|Kennison and Russell
|1987
PHP|Suppressed by a duplication carrying <fbsym>FBgn0003042==Pc</fbsym><up>+</up>.
}

REFDSR
{
RDID|FBrf0073734
|Lewis et al.
|1980
PHP|Transformation of meso- and metathoracic leg to prothoracic leg identity.
PHM|mesothoracic leg
|metathoracic leg
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Sex combs may be present on all six legs of male. At least
|one extra sex comb present in 75-90% of males. Third pair of
|legs less often affected than second.
|RK2.
PHM|sex comb
|mesothoracic leg
|metathoracic leg
}

REFDSR
{
RDID|FBrf0110811
|Sinclair et al.
|1984
PHP|Between 44.4% and 61.5% of heterozygous males have an extra sex combs
|phenotype.
PHM|leg
|sex comb | ectopic
}

REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0034841
|Kaufman et al.
|1980
REFM|FBrf0034853
|Lewis et al.
|1980
REFM|FBrf0039012
|Scott et al.
|1983
REFM|FBrf0043249
|Dura et al.
|1985
REFM|FBrf0046404
|Kennison and Russell
|1987
REFM|FBrf0073734
|Lewis et al.
|1980
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0110811
|Sinclair et al.
|1984
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002827	ICL 1 F	SYM 1 F{}ry-OreR	ASTR 1 -	CLOC 1 87D9	REF 1 2	DT 1 4 Feb 2000	RESZ 446
ID|FBti0002827
SYM|F{}ry-OreR
SYN|Jiminy
ASTP|<fbsym>FBtp0011425==F-element</fbsym>
DT|4 Feb 2000
|24 Jun 1997
ICL|F
ASGN|<fbsym>FBgn0003308==ry</fbsym>

REFDSR
{
RDID|FBrf0039845
|Bender et al.
|1983
SYN|Jiminy
CLOC|87D9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003308==ry</fbsym>
PHC|viable
CC|Found in Oregon-R strain at position -92 (FBrf0039845).
}

REF
{
REFM|FBrf0039845
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002828	ICL 1 roo	SYM 1 roo{}ry-OreR	ASTR 1 -	CLOC 1 87D9	REF 1 2	DT 1 4 Feb 2000	RESZ 451
ID|FBti0002828
SYM|roo{}ry-OreR
SYN|roo
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|4 Feb 2000
|24 Jun 1997
ICL|roo
ASGN|<fbsym>FBgn0003308==ry</fbsym>

REFDSR
{
RDID|FBrf0039845
|Bender et al.
|1983
SYN|roo
CLOC|87D9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003308==ry</fbsym>
PHC|viable
CC|Found segregating in Oregon-R strain at position -131 (FBrf0039845).
}

REF
{
REFM|FBrf0039845
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002829	ICL 1 Doc	SYM 1 Doc{}ry-OreR	ASTR 1 -	CLOC 1 87D9	REF 1 2	DT 1 4 Feb 2000	RESZ 450
ID|FBti0002829
SYM|Doc{}ry-OreR
SYN|Doc
ASTP|<fbsym>FBtp0011424==Doc</fbsym>
DT|4 Feb 2000
|24 Jun 1997
ICL|Doc
ASGN|<fbsym>FBgn0003308==ry</fbsym>

REFDSR
{
RDID|FBrf0039845
|Bender et al.
|1983
SYN|Doc
CLOC|87D9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003308==ry</fbsym>
PHC|viable
CC|Found segregating in Oregon-R strain at position -66 (FBrf0039845).
}

REF
{
REFM|FBrf0039845
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002830	ICL 1 Kermit	SYM 1 Kermit{}ry-CS	ASTR 1 -	CLOC 1 87D9	REF 1 2	DT 1 4 Feb 2000	RESZ 411
ID|FBti0002830
SYM|Kermit{}ry-CS
SYN|Kermit
DT|4 Feb 2000
|24 Jun 1997
ICL|Kermit
ASGN|<fbsym>FBgn0003308==ry</fbsym>

REFDSR
{
RDID|FBrf0039845
|Bender et al.
|1983
SYN|Kermit
CLOC|87D9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003308==ry</fbsym>
PHC|viable
CC|Found in Canton-S strain at position +10 (FBrf0039845).
}

REF
{
REFM|FBrf0039845
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0002832	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bxd-K</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 5	DT 1 4 Feb 2000	RESZ 554
ID|FBti0002832
SYM|gypsy{}Ubx<up>bxd-K</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|4 Feb 2000
|24 Jun 1997
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0040194
|Bender et al.
|1983
ASAL|<fbsym>FBal0017559==Ubx<up>bxd-K</up></fbsym>
ORI|+
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0040194
|Bender et al.
|1983
REFM|FBrf0051939
|Micol et al.
|1990
REFM|FBrf0051940
|Mathog
|1990
REFM|FBrf0057266
|Castelli-Gair et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0017559==Ubx<up>bxd-K</up></fbsym>

REFDSR
{
RDID|FBrf0040194
|Bender et al.
|1983
PHP|<fbsym>FBal0017559==Ubx<up>bxd-K</up></fbsym>/<fbsym>FBab0002687==Df(3R)Ubx109</fbsym> flies show
| variable loss of the first abdominal
|tergite and the posterior haltere is variably enlarged. These flies
|do not have extra legs.
PHM|abdominal tergite 1
|haltere | posterior
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Transformation of posterior portion of haltere toward wing,
|replacement of A1 tergite by post-notal tissue, no extra
|legs. A1 setal belt is intermediate between A1 and T3 type belts.
|Ventral pits on all abdominal segments.
PHM|abdominal segment 1
|abdominal segment 2
|abdominal segment 3
|abdominal segment 4
|abdominal segment 5
|abdominal segment 6
|abdominal segment 7
|haltere
|abdominal 1 ventral denticle belt
|abdominal tergite 1
|Kolbchen
}

REF
{
REFM|FBrf0040194
|Bender et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002949	ICL 1 P	SYM 1 P{PZ}gcm<up>P</up>	ASTR 1 +	CLOC 1 30B12	REF 1 3	DT 1 24 Jun 1997	RESZ 1339
ID|FBti0002949
SYM|P{PZ}gcm<up>P</up>
SYN|gcm<up>P</up>
|gcm<up>p</up>-lacZ
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|24 Jun 1997
|24 Jun 1997
ICL|P
ASGN|<fbsym>FBgn0014179==gcm</fbsym>
ARGS|FBgn0014179
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0001355==Ecol\lacZ<up>gcm-P</up>RA</fbsym>

REFDSR
{
RDID|FBrf0084044
|Hosoya et al.
|1995
ASAL|<fbsym>FBal0047719==Ecol\lacZ<up>gcm-P</up></fbsym>
|<fbsym>FBal0045763==gcm<up>P</up></fbsym>
CLOC|30B12
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0014179==gcm</fbsym>
CVBODPC|lacZ expression visible in whole cell body. No expression observed in
| midline glia.
CVBODP|transcript distribution deduced from reporter protein
|<t> E | stage >=11 <a> interface glial cell | precursor <p>
|<t> E | stage >=11 <a> neuroblast NB6-4 <p>
|<t> E | stage >=11 <a> medial-most cell body glial cell <p>
|<t> E | stage >=11 <a> glial cell <p>
|<t> E <a> peripheral nervous system <p>
|<t> E <a> embryonic brain <p>
|<t> E | cellular blastoderm <a>  <p>
CH|enhancer trap | <fbsym>FBgn0014179==gcm</fbsym>
}

REFDSR
{
RDID|FBrf0108424
|Akiyama-Oda et al.
|1999
SYN|gcm<up>p</up>-lacZ
}

REFDSR
{
RDID|FBrf0158873
|Shandala et al.
|2003
SYN|gcm<up>P</up>
}

REF
{
REFM|FBrf0084044
|Hosoya et al.
|1995
REFM|FBrf0108424
|Akiyama-Oda et al.
|1999
REFM|FBrf0158873
|Shandala et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0045763==gcm<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0084044
|Hosoya et al.
|1995
PHP|The CNS of heterozygous embryos is normal. Homozygous embryos exhibit
|defects in the formation of CNS axonal tracts.
PHM|central nervous system
}

REFDSR
{
RDID|FBrf0134555
|Takizawa and Hotta
|2001
PHP|Axonal elongations of the MP1/dMP2 and vMP2 neurons show no obvious
|abnormality in stage 13
| <fbsym>FBal0045763==gcm<up>P</up></fbsym>/<fbsym>FBal0045761==gcm<up>1</up></fbsym> embryos even
| though most
|of the misdifferentiated glial cells do not contact these longitudinal
|pioneer axons. Fasciculation of the MP1/dMP2 and vMP2 axons occurs
|normally in the absence of glial cells, although elongation is delayed
|and the fascicle looks thinner in some hemisegments.
PHM|(with gcm<up>1</up>) embryonic glial cell
|(with gcm<up>1</up>) longitudinal connective
}

REF
{
REFM|FBrf0084044
|Hosoya et al.
|1995
REFM|FBrf0134555
|Takizawa and Hotta
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002968	ICL 1 P	SYM 1 P{UAS-ptc.J}C	ASTR 1 -	CLOC 1 1-20	REF 1 3	DT 1 18 Jun 1998	RESZ 511
ID|FBti0002968
SYM|P{UAS-ptc.J}C
SYN|P(UAS-ptcC)
|UAS ptc C
ASTP|<fbsym>FBtp0001286==P{UAS-ptc.J}</fbsym>
DT|18 Jun 1998
|24 Jun 1997
ICL|P

REFDSR
{
RDID|FBrf0085299
|Johnson et al.
|1995
SYN|UAS ptc C
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REFDSR
{
RDID|FBrf0091570
|Johnson
|1997.3.15
SYN|P(UAS-ptcC)
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
PHC|viable
}

REF
{
REFM|FBrf0085299
|Johnson et al.
|1995
REFM|FBrf0091570
|Johnson
|1997.3.15
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0003089	ICL 1 P	SYM 1 P{lacW}N<up>Placr</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 3	DT 1 8 Oct 1997	RESZ 4594
ID|FBti0003089
SYM|P{lacW}N<up>Placr</up>
SYN|N[PlacW]
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0004647==N</fbsym>
SK|FBst0000009
|amx[1]/In(1)dl-49, m[2] g[4]
|FBst0000175
|y[1] pn[1] w[1] cm[1] ct[6] sn[3] oc[1] ras[2] v[1] dy[1] g[2] f[1] os[o] car[1] sw[1]/In(1)sc[S1], In(1)dl-49, y[c4] sc[S1] v[Of] B[1]
|FBst0000243
|In(1)dl-49, In(1)Hw[2], y[1] ac[Hw-2] m[2] g[4]/C(1)RM, y[1] w[1] f[1]
|FBst0000678
|Dp(1;1)Bx[r49k], v[1] f[1] Bx[r49k] car[1]/In(1)sc[S1], In(1)dl-49, sc[S1] v[1] f[1] B[1]
|FBst0000698
|In(1)dl-49, tyl[1] bb[l]/C(1)RM, y[1] v[1]
|FBst0000705
|C(1;Y)1, In(1)dl-49, y[1]; bw[1]; e[4]; ci[1] ey[R]
|FBst0000709
|Df(1)mal6, In(1)dl-49, In(1)B[M1], y[1] v[1] sn[X2] B[M1]/Dp(1;Y)y[+]mal[106], mal[106]/Df(1)mal3, y[2] ct[6] f[1], y[+]
|FBst0000778
|In(1)dl-49, tyl[1]
|FBst0000779
|In(1)dl-49, v[Of] f[1]
|FBst0000780
|In(1)dl-49, y[1] N[nd-0]
|FBst0000782
|In(1)dl-49, In(1)B[M1], sc[1] v[Of] B[M1]
|FBst0000793
|In(1)sc[7], In(1)AM, sc[7] ptg[4]/In(1)dl-49, y[1] ac[Hw-1] m[2] g[4]
|FBst0000799
|In(1)sc[8], In(1)dl-49, y[31d] sc[8]
|FBst0000948
|Df(1)ct-J4, In(1)dl-49, f[1]/C(1)DX, y[1] w[1] f[1]; Dp(1;3)sn[13a1]/+
|FBst0000973
|Df(1)mal10, In(1)sc[8], sc[8] B[1]/In(1)dl-49, v[1] sn[X2] mal[2]/Dp(1;Y)y[+]mal[106], mal[106]
|FBst0001035
|In(1)Mud, Mud[1]/In(1)dl-49, sn[X2]
|FBst0001110
|R(1;Y)EN, y[1]/In(1)dl-49, y[1] sc[1] w[1] g[2] f[1]; Dp(1;3)sc[J4], y[+]/+
|FBst0001394
|C(1;Y)1, In(1)dl-49, y[1] pn[62] v[Of] f[1]/0/C(1)M4
|FBst0001414
|In(1)pn[X], pn[X]/In(1)dl-49, y[1] Sxl[f1] v[Of] g[2]/Dp(1;Y)y[+]
|FBst0001418
|In(1)sc[4], y[1] sc[4] wy[74i] f[1] fu[1] car[1] ABO-X[1]/In(1)dl-49, y[1] ac[Hw-1] m[2] g[4]
|FBst0003226
|Df(1)cin-arth, In(1)sc[S1L]sc[8R], In(1)dl-49, w[a] v[Of] f[1]/C(1)DX, y[1] w[1] f[1]/Dp(1;Y)y[+]
|FBst0003753
|In(1)dl-49, y[1] sn[X2] bb[l]/In(1)sc[8], Df(1)mal, sc[8]
|FBst0003756
|In(1)sc[S1], In(1)S, sc[S1] B[1]/C(1;YS)1, In(1)dl-49, y[1] l(1)ml[1] w[1] f[1]
|FBst0003789
|In(1)sc[8], In(1)dl-49, y[S1] sc[8] v[Of] f[1] B[1]/In(1LR)sc[V1], sc[V1] v[Of]
|FBst0003896
|C(1)DX, y[1] f[1]/In(1)dl-49, Sxl[f1] oc[1] ptg[1] v[1]
|FBst0003963
|In(1)dl-49, Sxl[f1] v[Of] g[4]/R(YL)/C(1;YS)1, oc[1] ptg[1]
|FBst0003964
|In(1)dl-49, y[1] ac[Hw-1] m[2] g[4] f[5]/R(1)2, In(1)w[vC]
|FBst0003966
|In(1)dl-49, In(1)B[M1], oc[1] ptg[1] B[M1]/In(1)sc[S1L]sc[8R], y[c4] sc[8] sc[S1] w[1] sn[X2] sl[1]/R(YL)/C(1;YS)1, y[1] sn[1] oc[1] ptg[1] v[1]
|FBst0003968
|R(Y)F(9)/C(1;Y)1, In(1)dl-49, y[1] v[Of] f[1] car[1]
|FBst0004040
|C(1)DX, y[1] f[1]/In(1)dl-49, w[1] lz[s]
|FBst0004093
|C(1)RM, In(1)dl-49, y[1] ct[l] sn[X2]: y[1] ct[n] oc[1] ptg[1] car[1]/R(YL)/C(1;YS)1, oc[1] ptg[1]
|FBst0004338
|C(1)DX, y[1] f[1]/In(1)sc[S1L]sc[8R], In(1)dl-49, In(1)At, sc[8] sc[S1] w[a] v[Of] At[1]
|FBst0004443
|In(1)dl-49, y[1] w[1] lz[s]/In(1)sc[L8], sc[L8] w[a] m[2] car[1]
|FBst0004452
|C(1;YS)1, In(1)dl-49, y[1] v[Of] f[1]/Dp(1;YL)sc[S1]
|FBst0004462
|C(1;1;YS)RM[.]YS, In(1)EN, y[1]/C(1;Y)1, In(1)dl-49, y[1] v[Of] f[1] car[1]/0
|FBst0004475
|In(1)sc[8], In(1)dl-49, sc[8] v[Of] f[1] car[1]/C(1)DX, y[1] f[1]
|FBst0004480
|Dp(1;YS)sc[V1]/C(1;YL)1, In(1)dl-49, y[1] v[Of] B[1]/C(1)DX, y[1] f[1]
|FBst0004481
|C(1;YL)1, In(1)dl-49, v[Of] f[1] B[1]/F(YS)1/C(1)DX, y[1] f[1]
|FBst0004917
|y[2] wy[1] l(1)dd4[2] car[1]/In(1)sc[S1], In(1)dl-49, sc[S1] v[1] f[1] B[1]/Dp(1;Y)*, y[2] sc[+]
|FBst0005393
|ras[1] v[1] l(1)10Bm[1]/In(1)dl-49, ac[Hw-1] m[2] g[4]
|FBst0005670
|In(1)dl-49, y[1] w[1] M(1)15DEF[1:4C]/In(1)sc[8], lz[1] f[X] B[1]
|FBst0006019
|Df(1)w258-11, y[1]/In(1)dl-49, y[1] ac[Hw-1] m[2] g[4]
|FBst0006031
|Df(1)su(f)4B, In(1)sc[S1L]sc[8R], In(1)dl-49, y[c4] sc[8] sc[S1] w[a] v[1] f[1]/l(1)14[14]/Dp(1;Y)*
|FBst0006220
|Df(1)y-X15/In(1)dl-49, v[1] sn[X2] mal[2]
|FBst1001484
|Df(1)sc[4]/ In(1)dl-49, y[1] Hw [1] m[2] g[4]/y[2]Y67g
|FBst1001501
|FM6, f[x]/In(1)dl-49, y w lz[s]
|Total=46

REFDSR
{
RDID|FBrf0053371
|Ruohola et al.
|1991
SYN|P{lacW}N<up>Placr</up>
ASAL|<fbsym>FBal0029956==N<up>Placr</up></fbsym>
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
PHC|lethal | embryonic stage | neurogenic | recessive
}

REFDSR
{
RDID|FBrf0098438
|Heitzler
|1997
SYN|N[PlacW]
ABA|Aberration <fbsym>FBab0004116==In(1)dl-49</fbsym>
|Balancer <fbsym>FBba0000225==FM7h-N<up>Placr</up></fbsym>
CH|blue balancer | 1
|insertion on balancer | 1
CC|Original jump onto <fbsym>FBab0004116==In(1)dl-49</fbsym>; recombined onto <fbsym>FBba0000224==FM7h</fbsym>.
}

REF
{
REFM|FBrf0053371
|Ruohola et al.
|1991
REFM|FBrf0098438
|Heitzler
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0029956==N<up>Placr</up></fbsym>

REFDSR
{
RDID|FBrf0053371
|Ruohola et al.
|1991
PHP|Embryonic neurogenic phenotype and adult dominant wing phenotype.
PHM|embryonic nervous system
|embryonic nervous system | ectopic
|wing
}

REF
{
REFM|FBrf0053371
|Ruohola et al.
|1991
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003272	ICL 1 P	SYM 1 P{lacW}sax<up>P</up>	ASTR 1 -	CLOC 1 43E18	REF 1 2	DT 1 8 Oct 1997	RESZ 488
ID|FBti0003272
SYM|P{lacW}sax<up>P</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003317==sax</fbsym>

REFDSR
{
RDID|FBrf0074016
|Nellen et al.
|1994
SYN|P{lacW}sax<up>P</up>
ASAL|<fbsym>FBal0035538==sax<up>P</up></fbsym>
CLOC|43E18
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003317==sax</fbsym>
PHC|lethal | larval stage
|lethal | maternal effect
}

REF
{
REFM|FBrf0074016
|Nellen et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035538==sax<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0074016
|Nellen et al.
|1994
PHP|Female adult escapers are less viable than their heterozygous siblings.
|Rare embryos from these females show a phenotype similar to but milder
|and more variable than those from
| <fbsym>FBal0015142==sax<up>1</up></fbsym>/<fbsym>FBal0015143==sax<up>2</up></fbsym> females. Homozygous
|embryos are lacking the second midgut constriction. Homozygous females
|often lack the anterior crossvein, and the eyes are small due to reduced
|numbers of ommatidia.
PHM|amnioserosa | maternal effect
|midgut constriction 2
|anterior crossvein
|eye
|ommatidium
}

REFDSR
{
RDID|FBrf0103396
|Xie and Spradling
|1998
PHP|Germaria from one week old females are smaller than wild type and
|contain only one or two stem cells. Older females may have none, though
|though cysts and egg chambers remain.
PHM|germarium
|female germline stem cell
}

REF
{
REFM|FBrf0074016
|Nellen et al.
|1994
REFM|FBrf0103396
|Xie and Spradling
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003298	ICL 1 P	SYM 1 P{lacW}ttk<up>osn</up>	ASTR 1 -	CLOC 1 100D1	REF 1 3	DT 1 8 Oct 1997	RESZ 515
ID|FBti0003298
SYM|P{lacW}ttk<up>osn</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003870==ttk</fbsym>

REFDSR
{
RDID|FBrf0082058
|Guo et al.
|1995
SYN|P{lacW}ttk<up>osn</up>
ASAL|<fbsym>FBal0024415==ttk<up>osn</up></fbsym>
CLOC|100D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003870==ttk</fbsym>
PHC|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0082058
|Guo et al.
|1995
REFM|FBrf0094782
|Giesen et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0024415==ttk<up>osn</up></fbsym>

REFDSR
{
RDID|FBrf0082058
|Guo et al.
|1995
PHP|Overproduction of sensory neurons. Defects in the embryonic PNS, number
|of es and cho neurons is approximately doubled due to transformation
|of the outer support cell and cap cell respectively. Mosaic analysis
|demonstrates loss of <fbsym>FBgn0003870==ttk</fbsym> function in the adult leads to the
|appearance of supernumerary neurons at the expense of hair and socket
|cells.
PHM|embryonic peripheral nervous system
|thecogen cell & embryo
|scolopidial dendritic cap cell & embryo
|external sensory organ & adult | somatic clone
|socket & adult | somatic clone
|trichogen cell | somatic clone
|tormogen cell | somatic clone
}

REFDSR
{
RDID|FBrf0135902
|Okabe et al.
|2001
PHP|IIa precursor is transformed into a IIb precursor.
PHM|external sensory organ precursor cell IIa
|external sensory organ precursor cell IIb | supernumerary
}

REFDSR
{
RDID|FBrf0138359
|Pi et al.
|2001
PHP|Homozygotes have more sensory neurons than normal.
PHM|sensory neuron | supernumerary
}

REF
{
REFM|FBrf0082058
|Guo et al.
|1995
REFM|FBrf0135902
|Okabe et al.
|2001
REFM|FBrf0138359
|Pi et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003341	ICL 1 P	SYM 1 P{PZ}orb<up>dec</up>	ASTR 1 -	CLOC 1 94E1-94E10	REF 1 5	DT 1 8 Oct 1997	RESZ 1023
ID|FBti0003341
SYM|P{PZ}orb<up>dec</up>
SYN|fs(3)00107
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0004882==orb</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
SK|FBst0010326
|ry[506] P{ry[+t7.2]=PZ}orb[dec]/TM3,  ry[RK] Sb[1] Ser[1]
|Total=1

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|94E1-94E10
|Insertion site 
LOCB|in situ
}

REFDSR
{
RDID|FBrf0076495
|Lantz et al.
|1994
SYN|P{PZ}orb<up>dec</up>
ASAL|<fbsym>FBal0039709==orb<up>dec</up></fbsym>
CLOC|94E1-94E10
|Insertion site 
LOCB|in situ
PHC|female sterile
}

REFDSR
{
RDID|FBrf0076496
|Christerson and McKearin
|1994
ASAL|<fbsym>FBal0041809==Ecol\lacZ<up>orb-dec</up></fbsym>
PHC|female sterile
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
PHC|female sterile | recessive
}

REF
{
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0076495
|Lantz et al.
|1994
REFM|FBrf0076496
|Christerson and McKearin
|1994
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111489
|Spradling et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0039709==orb<up>dec</up></fbsym>

REFDSR
{
RDID|FBrf0076495
|Lantz et al.
|1994
PHP|Oogenesis has blocked during a stage of cyst development, the ovaries
|are very small and consist of germarium like structures populated by
|many small undifferentiated cells.
}

REFDSR
{
RDID|FBrf0076496
|Christerson and McKearin
|1994
PHP|Disrupts cyst formation near the time that the 16 cell cluster is formed
|and causes cyst degeneration. Ovaries are tiny, each ovariole consists
|of a germarium-like region and occasionally one or two egg chambers,
|egg chambers are often empty. Aberrant cellular morphology is seen
|in the germarial mid region, blebs appear on the surface of cystocytes
|(blebs are presumed to be the evidence of degenerating cells and cellular
|debris). <fbsym>FBal0039709==orb<up>dec</up></fbsym> interacts genetically with <fbsym>FBgn0003731==Egfr</fbsym>
| and <fbsym>FBgn0001137==grk</fbsym>, double
|... (see <fbsym>FBal0039709==orb<up>dec</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0089631
|Digilio et al.
|1996
PHM|ovary
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|female-sterile
|ovaries tumorous
}

REF
{
REFM|FBrf0076495
|Lantz et al.
|1994
REFM|FBrf0076496
|Christerson and McKearin
|1994
REFM|FBrf0089631
|Digilio et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003463	ICL 1 P	SYM 1 P{PZ}dac<up>P</up>	ASTR 1 +	CLOC 1 36A1-36A2	REF 1 11	DT 1 7 May 1998	RESZ 2329
ID|FBti0003463
SYM|P{PZ}dac<up>P</up>
SYN|P2047
|P{PZ}dac<up>rK364</up>
|P{PZ}l(2)rK364<up>rK364</up>
|P{PZ}rK364
|P{ry<up>+t7.2</up>=PZ}dac<up>rK364</up>
|P{ry<up>+t7.2</up>=PZ}l(2)rK364<up>rK364</up>
|dac-lacZ
|dacLacZ
|dac<up>10</up>lacZ
|l(2)rK364
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|7 May 1998
|8 Oct 1997
ICL|P
ID2|FBti0003024
|FBti0000455
ASGN|<fbsym>FBgn0005677==dac</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0004734==Ecol\lacZ<up>dac-P</up>RA</fbsym>
SK|FBst0012047
|P{ry[+t7.2]=PZ}dac[P]/CyO; ry[506]
|Total=1

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|36A1-36A2
|Insertion site 
LOCB|in situ
DBAF|AQ026135.1 5_Example.JPG
}

REFDSR
{
RDID|FBrf0075101
|Mardon et al.
|1994
ASAL|<fbsym>FBal0009297==dac<up>P</up></fbsym>
MU|P-element activity
ASAL|<fbsym>FBal0041048==Ecol\lacZ<up>dac-P</up></fbsym>
CLOC|36A1-36A2
|Insertion site 
LOCB|in situ
}

REFDSR
{
RDID|FBrf0083714
|Meister and Braun
|1995.10
SYN|P2047
CVBODPC|In third instar larva, expression in imaginal discs (which discs not specified).
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar stage 2 <a> imaginal disc <p>
}

REFDSR
{
RDID|FBrf0106052
|Wu and Cohen
|1999
SYN|dac-lacZ
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0111860
|Erkner et al.
|1999
SYN|dacLacZ
}

REFDSR
{
RDID|FBrf0112150
|Ashburner et al.
|1999
SYN|P{PZ}rK364
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0144840
|Chu et al.
|2002
SYN|dac-lacZ
}

REFDSR
{
RDID|FBrf0146985
|Dong et al.
|2002
SYN|dac-lacZ
}

REFDSR
{
RDID|FBrf0157204
|Galindo et al.
|2002
SYN|dac<up>10</up>lacZ
}

REFDSR
{
RDID|FBrf0184339
|FlyBase
|2005
SYN|P{PZ}dac<up>P</up>
CC|Location 2L:16481911-16481912 confirmed by FlyBase alignment of dbGSS
| accession AQ026135 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b.
}

REF
{
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0075101
|Mardon et al.
|1994
REFM|FBrf0083714
|Meister and Braun
|1995.10
REFM|FBrf0106052
|Wu and Cohen
|1999
REFM|FBrf0111489
|Spradling et al.
|1999
REFM|FBrf0111860
|Erkner et al.
|1999
REFM|FBrf0112150
|Ashburner et al.
|1999
REFM|FBrf0144840
|Chu et al.
|2002
REFM|FBrf0146985
|Dong et al.
|2002
REFM|FBrf0157204
|Galindo et al.
|2002
REFM|FBrf0184339
|FlyBase
|2005
}

ALESR
{
ASYM|<fbsym>FBal0009297==dac<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0075101
|Mardon et al.
|1994
PHP|Eyes of homozygotes are reduced and roughened. 50% of ommatidia have
|either too many or too few photoreceptors, and the ommatidial array
|is disrupted. Morphogenetic furrow movement is uneven, resulting in
|a curved furrow that has advanced further at midline than at the
|periphery of the disc. While legs have normal proximal and distal
|morphology, femur, tibia and proximal three tarsi are fused and
|condensed.
PHM|eye
|ommatidium
|photoreceptor cell R1
|photoreceptor cell R2
|photoreceptor cell R3
|photoreceptor cell R4
|photoreceptor cell R5
|photoreceptor cell R6
|photoreceptor cell R7
|photoreceptor cell R8
|leg
|eye-antennal disc
|morphogenetic furrow
}

REFDSR
{
RDID|FBrf0128567
|Martini et al.
|2000
PHP|Homozygous adults have a mild mushroom body phenotype. The eyes are
|consistently (but less severely than <fbsym>FBal0003921==ey<up>2</up></fbsym>) reduced in size.
PHM|mushroom body
|gamma-lobe
|eye
}

REF
{
REFM|FBrf0075101
|Mardon et al.
|1994
REFM|FBrf0128567
|Martini et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003499	ICL 1 P	SYM 1 P{PZ}Bsg<up>gel</up>	ASTR 1 +	CLOC 1 28D1-28D12	REF 1 5	DT 1 28 Apr 2005	RESZ 2228
ID|FBti0003499
SYM|P{PZ}Bsg<up>gel</up>
SYN|P1775
|P{PZ}gel<up>08318</up>
|P{PZ}gel<up>1</up>
|P{PZ}ms(2)08318<up>08318</up>
|ms(2)08318
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|28 Apr 2005
|8 Oct 1997
ICL|P
ID2|FBti0000232
ASGN|<fbsym>FBgn0011219==Bsg</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0004786==Ecol\lacZ<up>Bsg-gel</up>RA</fbsym>

REFDSR
{
RDID|FBrf0064394
|Castrillon et al.
|1993
SYN|P{PZ}gel<up>1</up>
ASAL|<fbsym>FBal0028203==Bsg<up>gel</up></fbsym>
MU|P-element activity
ASAL|<fbsym>FBal0041477==Ecol\lacZ<up>Bsg-gel</up></fbsym>
CLOC|28D1-28D12
|Insertion site 
LOCB|in situ
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|28D1-28D12
|Insertion site 
LOCB|in situ
DBAF|AQ026419.1 5_Example.JPG
}

REFDSR
{
RDID|FBrf0083714
|Meister and Braun
|1995.10
SYN|P1775
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar stage 2 <a> embryonic/larval proventriculus <p>
|<t> L | third instar stage 2 <a> embryonic/larval midgut | restricted <p>
|<t> L | third instar stage 2 <a> Malpighian tubule <p>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|male sterile
CC|This insertion was listed in the BDGP database as a lethal or sterile line
| during the period 1994-1999, but was not verified as such prior to the
| summary publication (FBrf0111489). Reasons for excluding lines from the
| collection described in FBrf0111489 include presence of more than one P
| insertion on the mutant chromosome, separation of lethality (or sterility)
| from the location of the insertion, and loss of lethality (or sterility)
| from the stock. Further information is available from
| <url>http://www.fruitfly.org/bfd/</url> and from Dr. Allan Spradling
| (spradlingmail1.ciwemb.edu). 
}

REFDSR
{
RDID|FBrf0184339
|FlyBase
|2005
SYN|P{PZ}Bsg<up>gel</up>
CC|Location 2L:8088275-8088276 confirmed by FlyBase alignment of dbGSS
| accession AQ026419 to D. melanogaster arm Release_4 and heterochromatin
| Release_3.2b. Insertion orientation confirmed.
}

REF
{
REFM|FBrf0064394
|Castrillon et al.
|1993
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0083714
|Meister and Braun
|1995.10
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184339
|FlyBase
|2005
}

}

# EOR

TIR
{

RETE|ID 1 FBti0003606	ICL 1 P	SYM 1 P{lacW}ph-p<up>lac</up>	ASTR 1 -	CLOC 1 2D2--3	REF 1 4	DT 1 8 Oct 1997	RESZ 767
ID|FBti0003606
SYM|P{lacW}ph-p<up>lac</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0004861==ph-p</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
SK|FBst0005443
|P{w[+mC]=lacW}ph-p[lac] w[1118]
|Total=1

REFDSR
{
RDID|FBrf0068212
|Fauvarque and Dura
|1994
ASAL|<fbsym>FBal0024620==ph-p<up>lac</up></fbsym>
MU|P-element activity
}

REFDSR
{
RDID|FBrf0079388
|Serrano et al.
|1995
SYN|P{lacW}ph-p<up>lac</up>
ASAL|<fbsym>FBal0044097==Ecol\lacZ<up>ph-p-lac</up></fbsym>
CLOC|2D2--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004861==ph-p</fbsym>
}

REF
{
REFM|FBrf0068212
|Fauvarque and Dura
|1994
REFM|FBrf0079388
|Serrano et al.
|1995
REFM|FBrf0083917
|Fauvarque et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0024620==ph-p<up>lac</up></fbsym>

REFDSR
{
RDID|FBrf0068212
|Fauvarque and Dura
|1994
PHP|Homozygous viable.
}

REFDSR
{
RDID|FBrf0079388
|Serrano et al.
|1995
PHP|Mild homeotic transformation.
}

REFDSR
{
RDID|FBrf0083917
|Fauvarque et al.
|1995
PHP|Transheterozygotes with a null <fbsym>FBgn0004861==ph-p</fbsym> allele or a deficiency of <fbsym>FBgn0004861==ph-p</fbsym>
|cause lethality.
}

REFDSR
{
RDID|FBrf0174557
|Narbonne et al.
|2004
PHP|<fbsym>FBal0024620==ph-p<up>lac</up></fbsym> homozygous females have egg chambers with
| abnormal numbers
|of germ cells. Egg chambers in these mutants with more than 16 germ
|cells (23% ovarioles contain at least one of these) sometimes contain
|groups of nurse cells with differing degrees of polyploidy, but all
|contain multiple oocytes. When an egg chamber contains fewer than
|15 nurse cells (5.6%), one of the adjacent chambers contains the complementary
|number of nurse cells or degenerating nurse cells. Whether follicles
|... (see <fbsym>FBal0024620==ph-p<up>lac</up></fbsym> report)
PHM|egg chamber
|germarium
|germarium region 3
|interfollicle cell
|interfollicle cell | ectopic
|polar follicle cell | ectopic
}

REF
{
REFM|FBrf0068212
|Fauvarque and Dura
|1994
REFM|FBrf0079388
|Serrano et al.
|1995
REFM|FBrf0083917
|Fauvarque et al.
|1995
REFM|FBrf0174557
|Narbonne et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003612	ICL 1 P	SYM 1 P{lArB}wg<up>NZ</up>	ASTR 1 -	CLOC 1 27F1	REF 1 3	DT 1 8 Oct 1997	RESZ 583
ID|FBti0003612
SYM|P{lArB}wg<up>NZ</up>
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0004009==wg</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0079914
|Buratovich and Bryant
|1995
SYN|P{lArB}wg<up>NZ</up>
ASAL|<fbsym>FBal0044126==Ecol\lacZ<up>wg-NZ</up></fbsym>
|<fbsym>FBal0044466==wg<up>NZ</up></fbsym>
CLOC|27F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004009==wg</fbsym>
}

REF
{
REFM|FBrf0079914
|Buratovich and Bryant
|1995
REFM|FBrf0093385
|Buratovich et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0044466==wg<up>NZ</up></fbsym>

REFDSR
{
RDID|FBrf0079914
|Buratovich and Bryant
|1995
PHP|<fbsym>FBal0018508==wg<up>l-16</up></fbsym>/<fbsym>FBal0044466==wg<up>NZ</up></fbsym> heterozygotes
| display leg pattern element disruptions.
}

REFDSR
{
RDID|FBrf0128473
|Garoia et al.
|2000
PHP|<fbsym>FBal0044466==wg<up>NZ</up></fbsym> causes lack of sensory elements in the wing margin.
|<fbsym>FBal0044466==wg<up>NZ</up></fbsym>/<fbsym>FBal0035084==ft<up>k07918</up></fbsym> somatic clones
| exhibit an additive phenotype
|of the two alleles.
PHM|wing margin bristle
}

REF
{
REFM|FBrf0079914
|Buratovich and Bryant
|1995
REFM|FBrf0128473
|Garoia et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003614	ICL 1 P	SYM 1 P{wF}mas<up>P</up>	ASTR 1 -	CLOC 1 64A8	REF 1 4	DT 1 13 Sep 1999	RESZ 968
ID|FBti0003614
SYM|P{wF}mas<up>P</up>
SYN|P<up>(w,ry)F</up>3
|P{wF}3
|P{w<up>+mF</up> ry<up>+t7.2</up>=wF}3
|P{w<up>F</up> ry<up>+t7.2</up>=wF}3
|P{white-un1}mas<up>P</up>
ASTP|<fbsym>FBtp0000086==P{wF}</fbsym>
DT|13 Sep 1999
|8 Oct 1997
ICL|P
ID2|FBti0001609
|FBti0003050
|FBti0001332
ASGN|<fbsym>FBgn0011653==mas</fbsym>
SK|FBst0005152
|w[1118]; P{w[+mF] ry[+t7.2]=wF}mas[P] ry[506]/TM3, ry[RK] Sb[1] Ser[1]
|Total=1

REFDSR
{
RDID|FBrf0042436
|Levis et al.
|1985
SYN|P<up>(w,ry)F</up>3
CLOC|64A8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011653==mas</fbsym>
}

REFDSR
{
RDID|FBrf0080274
|Murugasu-Oei et al.
|1995
SYN|P{white-un1}mas<up>P</up>
ASAL|<fbsym>FBal0044170==mas<up>P</up></fbsym>
CLOC|64A8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011653==mas</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0042436
|Levis et al.
|1985
REFM|FBrf0080274
|Murugasu-Oei et al.
|1995
REFM|FBrf0089757
|Murugasu-Oei et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0044170==mas<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0080274
|Murugasu-Oei et al.
|1995
PHP|Defective chemosensory perception in third instar larvae and adults.
}

REFDSR
{
RDID|FBrf0089757
|Murugasu-Oei et al.
|1996
PHP|Gustatory behavior: reduced sensitivity to sucrose. Reduced feeding
|is due to reduced performance of the gustatory circuits, not a disinclination
|to feed as demonstrated by the proboscis extension reflex. Fails to
|respond to low concentrations of NaCl but rejection of high concentrations
|of NaCl and KCl is not significantly different from wild-type; defect
|in the assessment of salt concentration.
}

REF
{
REFM|FBrf0080274
|Murugasu-Oei et al.
|1995
REFM|FBrf0089757
|Murugasu-Oei et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003682	ICL 1 P	SYM 1 P{lwB}en<up>AuI</up>	ASTR 1 +	CLOC 1 -	REF 1 3	DT 1 5 Feb 1999	RESZ 1591
ID|FBti0003682
SYM|P{lwB}en<up>AuI</up>
SYN|Au1
|AuI
|P{lacW}AuI
|P{lacW}en<up>AuI</up>
|P{lacZ}AuI
|P{lwB}Au1
ASTP|<fbsym>FBtp0000157==P{lwB}</fbsym>
DT|5 Feb 1999
|8 Oct 1997
ICL|P
ID2|FBti0002688
|FBti0009166
PRG|P{lwB}56B
ASGN|<fbsym>FBgn0000577==en</fbsym>
|<fbsym>FBgn0003996==w</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0000406==Ecol\lacZ<up>en-AuI</up>RA</fbsym>
SK|FBst0006942
|w[*]; P{w[+mW.hs]=lwB}en[AuI]/CyO
|Total=1

REFDSR
{
RDID|FBrf0053395
|Klambt et al.
|1991
SYN|Au1
ASAL|<fbsym>FBal0047662==Ecol\lacZ<up>en-AuI</up></fbsym>
CVBODPC|Enhancer trap expression is observed only in the posterior pair of midline
| glia (MGP).
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> midline glial cell <p>
}

REFDSR
{
RDID|FBrf0068598
|Menne and Klambt
|1994
SYN|P{lacZ}AuI
ASAL|<fbsym>FBal0047662==Ecol\lacZ<up>en-AuI</up></fbsym>
}

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
SYN|AuI
|P{lacW}en<up>AuI</up>
ASAL|<fbsym>FBal0047662==Ecol\lacZ<up>en-AuI</up></fbsym>
|<fbsym>FBal0045592==en<up>AuI</up></fbsym>
|<fbsym>FBal0046733==w<up>AuI</up></fbsym>
CVBODPC|In embryo, "patterned" expression.
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a>  <p>
|<t> L | third instar <a> antennal disc | restricted <p>
|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
|<t> L | third instar <a> ventral thoracic disc | restricted <p>
CH|enhancer trap | <fbsym>FBgn0000577==en</fbsym>
}

REF
{
REFM|FBrf0053395
|Klambt et al.
|1991
REFM|FBrf0068598
|Menne and Klambt
|1994
REFM|FBrf0084424
|Sun et al.
|1995
}

ALESR
{
ASYM|<fbsym>FBal0046733==w<up>AuI</up></fbsym>

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
PHP|Eye pigment distribution: anteroventral sector.
PHM|pigment cell
}

REF
{
REFM|FBrf0084424
|Sun et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003707	ICL 1 P	SYM 1 P{lacW}jim<up>OVK</up>	ASTR 1 +	CLOC 1 -	REF 1 4	DT 1 6 Jan 2000	RESZ 1049
ID|FBti0003707
SYM|P{lacW}jim<up>OVK</up>
SYN|P{lacW}ovfc.K<up>1</up>
|P{lacW}ovk
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|6 Jan 2000
|8 Oct 1997
ICL|P
ID2|FBti0009865
ASGN|<fbsym>FBgn0027339==jim</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0006089==Ecol\lacZ<up>jim-OVK</up>RA</fbsym>

REFDSR
{
RDID|FBrf0067197
SYN|P{lacW}ovk
}

REFDSR
{
RDID|FBrf0084964
|Doerflinger et al.
|1996
SYN|P{lacW}ovfc.K<up>1</up>
ASAL|<fbsym>FBal0046235==jim<up>OVK</up></fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ASAL|<fbsym>FBal0086457==Ecol\lacZ<up>jim-OVK</up></fbsym>
}

REFDSR
{
RDID|FBrf0111357
|Doerflinger et al.
|1999
CVBODPC|Enhancer trap expression is observed from stage 10 of oogenesis specifically
| in the non-antero-dorsal columnar follicle cells.
CVBODP|transcript distribution deduced from reporter protein
|<t> O,A | stage >=S10 <a> oocyte associated follicle cell <p>
}

REF
{
REFM|FBrf0067197
REFM|FBrf0084964
|Doerflinger et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111357
|Doerflinger et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0046235==jim<up>OVK</up></fbsym>

REFDSR
{
RDID|FBrf0086754
|Doerflinger
|1996.4.29
PHP|No detectable phenotype.
}

REFDSR
{
RDID|FBrf0111357
|Doerflinger et al.
|1999
PHP|17% of the eggs laid by homozygous females do not hatch, compared to
|7% in wildtype.
}

REF
{
REFM|FBrf0086754
|Doerflinger
|1996.4.29
REFM|FBrf0111357
|Doerflinger et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003750	ICL 1 P	SYM 1 P{lacW}AG	ASTR 1 +	CLOC 1 86E6-86E8	REF 1 1	DT 1 8 Oct 1997	RESZ 598
ID|FBti0003750
SYM|P{lacW}AG
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0003765==Ecol\lacZ<up>AG</up>RA</fbsym>

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
SYN|P{lacW}AG
ASAL|<fbsym>FBal0047275==Ecol\lacZ<up>AG</up></fbsym>
|<fbsym>FBal0046731==w<up>AG</up></fbsym>
CLOC|86E6-86E8
|Insertion site 
LOCB|in situ
CVBODPC|In embryo, "patterned" expression.
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a>  <p>
}

REF
{
REFM|FBrf0084424
|Sun et al.
|1995
}

ALESR
{
ASYM|<fbsym>FBal0046731==w<up>AG</up></fbsym>

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
PHP|Eye pigment distribution: anteroposterior gradient.
PHM|pigment cell
}

REF
{
REFM|FBrf0084424
|Sun et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003758	ICL 1 P	SYM 1 P{lacW}PD	ASTR 1 +	CLOC 1 17A1-17A6	REF 1 4	DT 1 8 Oct 1997	RESZ 1087
ID|FBti0003758
SYM|P{lacW}PD
SYN|PD
|upd-lacZ
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0003789==Ecol\lacZ<up>os-PD</up>RA</fbsym>

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
SYN|P{lacW}PD
ASAL|<fbsym>FBal0047457==Ecol\lacZ<up>os-PD</up></fbsym>
|<fbsym>FBal0046759==w<up>PD</up></fbsym>
CLOC|17A1-17A6
|Insertion site 
LOCB|in situ
CVBODPC|In embryo, "patterned" expression.  In larva, <fbsym>FBgn0014447==Ecol\lacZ</fbsym> expression in leg
| disc is relatively weak.
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a>  <p>
|<t> L | third instar <a> eye disc | restricted <p>
|<t> L | third instar <a> ventral thoracic disc | restricted <p>
}

REFDSR
{
RDID|FBrf0108427
|Reifegerste and Moses
|1999
SYN|PD
}

REFDSR
{
RDID|FBrf0179159
|Chao et al.
|2004
SYN|PD
|upd-lacZ
}

REF
{
REFM|FBrf0084424
|Sun et al.
|1995
REFM|FBrf0108427
|Reifegerste and Moses
|1999
REFM|FBrf0141754
|Tulina and Matunis
|2001
REFM|FBrf0179159
|Chao et al.
|2004
}

ALESR
{
ASYM|<fbsym>FBal0046759==w<up>PD</up></fbsym>

REFDSR
{
RDID|FBrf0084424
|Sun et al.
|1995
PHP|Eye pigment distribution: posterior dot.
PHM|pigment cell
}

REF
{
REFM|FBrf0084424
|Sun et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0003936	ICL 1 P	SYM 1 P{GawB}tracheal	ASTR 1 +	CLOC 1 -	REF 1 7	DT 1 8 Oct 1997	RESZ 1195
ID|FBti0003936
SYM|P{GawB}tracheal
SYN|TRA-GAL4
|TrGal4
|tr-Gal4
|tracheal-Gal4
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0014445==Scer\GAL4</fbsym>
ASTR|<fbsym>FBtr0005582==Scer\GAL4<up>tracheal</up>RA</fbsym>

REFDSR
{
RDID|FBrf0087274
|Guillemin et al.
|1996
SYN|P{GawB}tracheal
ASAL|<fbsym>FBal0048795==Scer\GAL4<up>tracheal</up></fbsym>
}

REFDSR
{
RDID|FBrf0090661
|Lee et al.
|1996
CVBODP|transcript distribution deduced from reporter protein distribution, binary system (Gal4 UAS)
|<t> E | stage >=13 <a> embryonic/larval trachea <p>
}

REFDSR
{
RDID|FBrf0100567
|Hacohen et al.
|1998
SYN|TrGal4
CVBODPC|Expressed in all embryonic tracheal cells, from stage 13 on.
}

REFDSR
{
RDID|FBrf0108514
|Llimargas
|1999
SYN|tr-Gal4
}

REFDSR
{
RDID|FBrf0135726
|Glazer and Shilo
|2001
SYN|tracheal-Gal4
}

REFDSR
{
RDID|FBrf0167462
|Parsons et al.
|2003
SYN|TRA-GAL4
}

REF
{
REFM|FBrf0087274
|Guillemin et al.
|1996
REFM|FBrf0090661
|Lee et al.
|1996
REFM|FBrf0090781
|Samakovlis et al.
|1996
REFM|FBrf0100567
|Hacohen et al.
|1998
REFM|FBrf0108514
|Llimargas
|1999
REFM|FBrf0135726
|Glazer and Shilo
|2001
REFM|FBrf0167462
|Parsons et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0003946	ICL 1 P	SYM 1 P{UAS-lacZ.B}Ubx<up>Scer\UASlacZ</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 9 May 1999	RESZ 529
ID|FBti0003946
SYM|P{UAS-lacZ.B}Ubx<up>Scer\UASlacZ</up>
SYN|P{UAS-lacZ.B}Ubx<up>UASlacZ</up>
ASTP|<fbsym>FBtp0000355==P{UAS-lacZ.B}</fbsym>
DT|9 May 1999
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0086537
|McCall and Bender
|1996
SYN|P{UAS-lacZ.B}Ubx<up>UASlacZ</up>
ASAL|<fbsym>FBal0049248==Ubx<up>Scer\UASlacZ</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
}

REF
{
REFM|FBrf0086537
|McCall and Bender
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004002	ICL 1 P	SYM 1 P{PZ}wg<up>Sp-revP</up>	ASTR 1 +	CLOC 1 27F1	REF 1 1	DT 1 8 Oct 1997	RESZ 899
ID|FBti0004002
SYM|P{PZ}wg<up>Sp-revP</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
PRG|<fbsym>FBti0002727==P{PZ}wg<up>rO727</up></fbsym>
ASGN|<fbsym>FBgn0004009==wg</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0001517==Ecol\lacZ<up>wg-Sp-revP</up>RA</fbsym>

REFDSR
{
RDID|FBrf0087628
|Neumann and Cohen
|1996
SYN|P{PZ}wg<up>Sp-revP</up>
ASAL|<fbsym>FBal0050095==Ecol\lacZ<up>wg-Sp-revP</up></fbsym>
|<fbsym>FBal0050823==wg<up>Sp-revP</up></fbsym>
CLOC|27F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004009==wg</fbsym>
CVBODPC|Reflects pattern of <fbsym>FBgn0004009==wg</fbsym> expression in wing disc.
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar <a> dorsal mesothoracic disc | restricted <p>
CH|enhancer trap
PHC|lethal | pupal stage | recessive
}

REF
{
REFM|FBrf0087628
|Neumann and Cohen
|1996
}

ALESR
{
ASYM|<fbsym>FBal0050823==wg<up>Sp-revP</up></fbsym>

REFDSR
{
RDID|FBrf0087628
|Neumann and Cohen
|1996
PHP|The dominant Sp phenotype is almost completely suppressed, 10% of individuals
|exhibit a mild Sp phenotype. Individuals in combination with <fbsym>FBal0015984==wg<up>Sp-1</up></fbsym>,
|<fbsym>FBal0050829==wg<up>spd-j2</up></fbsym>, <fbsym>FBal0018510==wg<up>P</up></fbsym> and
| <fbsym>FBal0018508==wg<up>l-16</up></fbsym> are pupal lethal. Individuals
|are adult viable and exhibit the wing phenotype when in combination
|with <fbsym>FBal0018482==wg<up>1</up></fbsym>. When in combination with
| <fbsym>FBal0018509==wg<up>l-17</up></fbsym> individuals are
|pupal lethal, pharate escapers lack antennae, legs and anterior dorsocentrals.
PHM|sternopleural bristle
}

REF
{
REFM|FBrf0087628
|Neumann and Cohen
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004010	ICL 1 P	SYM 1 P{Bm&Dgr;-w}pyd<up>tam</up>	ASTR 1 -	CLOC 1 85B2--7	REF 1 2	DT 1 26 Aug 1998	RESZ 509
ID|FBti0004010
SYM|P{Bm&Dgr;-w}pyd<up>tam</up>
SYN|P{BmDelta-w}tam<up>1</up>
ASTP|<fbsym>FBtp0000774==P{Bm&Dgr;-w}</fbsym>
DT|26 Aug 1998
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003177==pyd</fbsym>
ARGS|FBgn0003177

REFDSR
{
RDID|FBrf0089841
|Takahisa et al.
|1996
SYN|P{BmDelta-w}tam<up>1</up>
ASAL|<fbsym>FBal0051070==pyd<up>tam</up></fbsym>
CLOC|85B2--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003177==pyd</fbsym>
}

REF
{
REFM|FBrf0089841
|Takahisa et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0051070==pyd<up>tam</up></fbsym>

REFDSR
{
RDID|FBrf0089841
|Takahisa et al.
|1996
PHP|Ectopic macrochaetae are present on the dorsal surface of the adult
|head and thorax. Extra sensilla campaniformia develop on the wing
|vein.
PHM|macrochaeta & adult head | dorsal
|macrochaeta & adult thorax | dorsal
|wing sensillum
}

REFDSR
{
RDID|FBrf0105943
|Takahashi et al.
|1998
PHP|Homozygous embryos develop normally.
|Homozygous adults have a normal dorsal thorax.
|Homozygous <fbsym>FBal0005438==hep<up>1</up></fbsym> adults show slight widening of the
| dorsal thorax.
}

REF
{
REFM|FBrf0089841
|Takahisa et al.
|1996
REFM|FBrf0105943
|Takahashi et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004027	ICL 1 P	SYM 1 P{KZ.TRAP}rp	ASTR 1 +	CLOC 1 21-60	REF 1 1	DT 1 8 Oct 1997	RESZ 769
ID|FBti0004027
SYM|P{KZ.TRAP}rp
SYN|KZrp
ASTP|<fbsym>FBtp0001242==P{KZ.TRAP}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0003761==Ecol\lacZ<up>rp</up>RA</fbsym>

REFDSR
{
RDID|FBrf0083232
|Kolodziej et al.
|1995
SYN|KZrp
|P{KZ.TRAP}rp
ASAL|<fbsym>FBal0052248==Ecol\lacZ<up>rp</up></fbsym>
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
CVBODPC|In late embryos, &bgr;-gal signal observed in the a subset of longitudinal
| and commissural axons of the CNS, and in a subset of the segmental nerve
| motor axons of the PNS.
CVBODP|transcript distribution deduced from reporter protein
|<t> E | late <a> embryonic nervous system | restricted <p>
PHC|viable
}

REF
{
REFM|FBrf0083232
|Kolodziej et al.
|1995
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004073	ICL 1 P	SYM 1 P{FRT(w<up>hs</up>)}TD	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 10 May 1999	RESZ 450
ID|FBti0004073
SYM|P{FRT(w<up>hs</up>)}TD
SYN|P{>w<up>hs</up>>}TD
ASTP|<fbsym>FBtp0000268==P{FRT(w<up>hs</up>)}</fbsym>
DT|10 May 1999
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0090428
|Ahmad and Golic
|1996
SYN|P{>w<up>hs</up>>}TD
ASAL|<fbsym>FBal0055885==w<up>TD</up></fbsym>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0090428
|Ahmad and Golic
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0055885==w<up>TD</up></fbsym>

REFDSR
{
RDID|FBrf0090428
|Ahmad and Golic
|1996
PHP|In a <fbsym>FBal0018186==w<up>1118</up></fbsym> background eyes exhibit lack of pigment
| in the dorsal
|one-fifth of the eye and at the most ventral posterior edge.
PHM|eye
}

REF
{
REFM|FBrf0090428
|Ahmad and Golic
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004077	ICL 1 P	SYM 1 P{lArB}sca<up>P</up>	ASTR 1 -	CLOC 1 49C3--D3	REF 1 2	DT 1 8 Oct 1997	RESZ 441
ID|FBti0004077
SYM|P{lArB}sca<up>P</up>
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003326==sca</fbsym>

REFDSR
{
RDID|FBrf0090681
|Mackay and Fry
|1996
SYN|P{lArB}sca<up>P</up>
ASAL|<fbsym>FBal0056193==sca<up>P</up></fbsym>
CLOC|49C3--D3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003326==sca</fbsym>
}

REF
{
REFM|FBrf0090681
|Mackay and Fry
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004084	ICL 1 P	SYM 1 P{lacW}mwr<up>a</up>	ASTR 1 -	CLOC 1 50C1--6	REF 1 2	DT 1 8 Oct 1997	RESZ 505
ID|FBti0004084
SYM|P{lacW}mwr<up>a</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0019668==mwr</fbsym>

REFDSR
{
RDID|FBrf0091150
|Rasooly
|1996
SYN|P{lacW}mwr<up>a</up>
ASAL|<fbsym>FBal0056460==mwr<up>a</up></fbsym>
CLOC|50C1--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0019668==mwr</fbsym>
PHC|lethal | partially
|lethal | embryonic stage | maternal effect | recessive
}

REF
{
REFM|FBrf0091150
|Rasooly
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0056460==mwr<up>a</up></fbsym>

REFDSR
{
RDID|FBrf0091150
|Rasooly
|1996
PHP|Homozygous females are completely sterile, eggs that are laid are grossly
|normal but fail to hatch. Females heterozygous with
| <fbsym>FBal0056460==mwr<up>a</up></fbsym> excision
|alleles (<fbsym>FBal0056464==mwr<up>1</up></fbsym>, <fbsym>FBal0056463==mwr<up>2</up></fbsym>,
| <fbsym>FBal0056462==mwr<up>3</up></fbsym> or <fbsym>FBal0056461==mwr<up>4</up></fbsym>) are nearly or completely
|sterile.
|Mutation impairs segregation of nonexchange chromosomes. Meiotic defect
|is in homologue recognition as the chromosomes appear to be misaligned
|on an intact spindle.
}

REF
{
REFM|FBrf0091150
|Rasooly
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004089	ICL 1 P	SYM 1 P{lwB}fru<up>sat</up>	ASTR 1 -	CLOC 1 91A7--B3	REF 1 5	DT 1 8 Oct 1997	RESZ 1201
ID|FBti0004089
SYM|P{lwB}fru<up>sat</up>
ASTP|<fbsym>FBtp0000157==P{lwB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0004652==fru</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0082170
|Ito et al.
|1995
ASAL|<fbsym>FBal0031286==fru<up>sat</up></fbsym>
MU|P-element activity
}

REFDSR
{
RDID|FBrf0090624
|Ito et al.
|1996
SYN|P{lwB}fru<up>sat</up>
ASAL|<fbsym>FBal0056680==Ecol\lacZ<up>fru-sat</up></fbsym>
CLOC|91A7--B3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004652==fru</fbsym>
}

REFDSR
{
RDID|FBrf0125440
|Goodwin et al.
|2000
PHC|sterile | recessive
}

REFDSR
{
RDID|FBrf0130128
|Usui-Aoki et al.
|2000
PHC|(with fru<up>AM.hs</up>) lethal | conditional ts
|(with fru<up>BM.Scer\UAS.cUa</up>) lethal with <fbsym>FBal0047062==Scer\GAL4<up>D42</up></fbsym>
|(with fru<up>B.Scer\UAS.cUa</up>) semi-lethal with <fbsym>FBal0047062==Scer\GAL4<up>D42</up></fbsym>
|(with fru<up>E.Scer\UAS.cUa</up>) semi-lethal with <fbsym>FBal0047062==Scer\GAL4<up>D42</up></fbsym>
}

REF
{
REFM|FBrf0082170
|Ito et al.
|1995
REFM|FBrf0090624
|Ito et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125440
|Goodwin et al.
|2000
REFM|FBrf0130128
|Usui-Aoki et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0031286==fru<up>sat</up></fbsym>

REFDSR
{
RDID|FBrf0082170
|Ito et al.
|1995
PHP|Males are homosexual, only courting with males. Heterozygotes with
|<fbsym>FBab0005763==In(3R)fru</fbsym> are bisexual.
}

REFDSR
{
RDID|FBrf0090624
|Ito et al.
|1996
PHP|Homozygous males do not court with either homozygous
| <fbsym>FBal0031286==fru<up>sat</up></fbsym> or
|wild-type females, whereas homozygous <fbsym>FBal0031286==fru<up>sat</up></fbsym> females
| are highly
|receptive to courting by wild-type males.
| <fbsym>FBal0004157==fru<up>1</up></fbsym>/<fbsym>FBal0031286==fru<up>sat</up></fbsym> males
|mate with females, although less often than wild-type males do, and
|they are fertile. Homozygous <fbsym>FBal0031286==fru<up>sat</up></fbsym> and
| <fbsym>FBal0004157==fru<up>1</up></fbsym>/<fbsym>FBal0031286==fru<up>sat</up></fbsym> males
|form courtship chains. Homozygous <fbsym>FBal0031286==fru<up>sat</up></fbsym> males lack
| the muscle
|of Lawrence.
|... (see <fbsym>FBal0031286==fru<up>sat</up></fbsym> report)
PHM|male abdominal 5 muscle
}

REFDSR
{
RDID|FBrf0125440
|Goodwin et al.
|2000
PHP|Males show low levels of courtship, with either
| <fbsym>FBal0031286==fru<up>sat</up></fbsym> males or
|wild type females. Residual courtship is not normal. Sine-song bouts
|are short and no song pulses are generated. Mutant males exhibit tapping
|and licking but no attempted copulation. Males grouped together display
|courtship chaining with numerous wing extensions.
|Sterile over <fbsym>FBab0002629==Df(3R)P14</fbsym> and <fbsym>FBab0026872==Df(3R)fru<up>w24</up></fbsym> with
| occasional fertile
|heterozygotes over <fbsym>FBab0022392==Df(3R)Cha<up>M5</up></fbsym>.
|... (see <fbsym>FBal0031286==fru<up>sat</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0130128
|Usui-Aoki et al.
|2000
PHP|Males show male preference in courtship and completely lack the muscle
|of Lawrence.
|Expression of <fbsym>FBal0144303==fru<up>AM.hs</up></fbsym> using heat shock during
| either the embryo
|to third larval instar or during the third larval instar to pupal stage
|results in lethality in <fbsym>FBal0031286==fru<up>sat</up></fbsym> males.
|Expression of <fbsym>FBal0144301==fru<up>B.Scer\UAS.cUa</up></fbsym> under the control of <fbsym>FBal0047062==Scer\GAL4<up>D42</up></fbsym>
|in <fbsym>FBal0031286==fru<up>sat</up></fbsym> females results in the formation of the
| muscle of Lawrence
|... (see <fbsym>FBal0031286==fru<up>sat</up></fbsym> report)
PHM|male abdominal 5 muscle
|(with fru<up>B.Scer\UAS.cUa</up>) male abdominal 5 muscle | ectopic | female with <fbsym>FBal0047062==Scer\GAL4<up>D42</up></fbsym>
}

REFDSR
{
RDID|FBrf0134454
|Lee and Hall
|2000
PHP|Homozygous males show high levels of head-to-head interactions compared
|to wild-type males. Most of these would-be aggressive actions involve
|bringing their heads together but not escalating the interactions into
|the rising-up and boxing motions that are displayed by wild-type males.
|The level of head-to-head interactions shows a temporal dependency;
|when males are grouped together on the day they eclose they do not
|show significantly higher than normal head-to-head interactions, but
|... (see <fbsym>FBal0031286==fru<up>sat</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0134722
|Lee and Hall
|2001
PHP|Expression of 5-HT in serotonergic-abdominal ganglion neurons in adult
|males is defective; relatively few neurons express 5-HT compared to
|wild type.
}

REF
{
REFM|FBrf0082170
|Ito et al.
|1995
REFM|FBrf0090624
|Ito et al.
|1996
REFM|FBrf0125440
|Goodwin et al.
|2000
REFM|FBrf0130128
|Usui-Aoki et al.
|2000
REFM|FBrf0134454
|Lee and Hall
|2000
REFM|FBrf0134722
|Lee and Hall
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004092	ICL 1 P	SYM 1 P{PZ}byn<up>apro</up>	ASTR 1 +	CLOC 1 68E3	REF 1 5	DT 1 8 Oct 1997	RESZ 1438
ID|FBti0004092
SYM|P{PZ}byn<up>apro</up>
SYN|Byn-lacZ
|byn-lacZ
|byn<up>apro</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0011723==byn</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0007242==Ecol\lacZ<up>byn-apro</up>RA</fbsym>

REFDSR
{
RDID|FBrf0077493
|Murakami et al.
|1994
SYN|P{PZ}byn<up>apro</up>
ASAL|<fbsym>FBal0057714==byn<up>apro</up></fbsym>
|<fbsym>FBal0056701==Ecol\lacZ<up>byn-apro</up></fbsym>
CLOC|68E3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011723==byn</fbsym>
}

REFDSR
{
RDID|FBrf0084211
|Murakami et al.
|1995
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0111436
|Moreno and Morata
|1999
SYN|byn-lacZ
CLOC|68E3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011723==byn</fbsym>
CVBODP|transcript distribution deduced from reporter protein
|<t> A <a> hindgut <p>
}

REFDSR
{
RDID|FBrf0151948
|Johansen et al.
|2003
SYN|byn<up>apro</up>
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> embryonic hindgut <p>  <s> nucleus <c>  <l>
}

REFDSR
{
RDID|FBrf0178997
|Copf et al.
|2003
SYN|Byn-lacZ
CVBODP|transcript distribution deduced from reporter protein
|<t> L <a> dorsal mesothoracic disc | restricted <p>
}

REF
{
REFM|FBrf0077493
|Murakami et al.
|1994
REFM|FBrf0084211
|Murakami et al.
|1995
REFM|FBrf0111436
|Moreno and Morata
|1999
REFM|FBrf0151948
|Johansen et al.
|2003
REFM|FBrf0178997
|Copf et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0057714==byn<up>apro</up></fbsym>

REFDSR
{
RDID|FBrf0084211
|Murakami et al.
|1995
PHP|Degeneration of the proctodeum during shortening of the germ band stage.
PHM|proctodeum
}

REF
{
REFM|FBrf0084211
|Murakami et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004135	ICL 1 P	SYM 1 P{hsneo}ifc<up>des</up>	ASTR 1 -	CLOC 1 26B2	REF 1 2	DT 1 8 Oct 1997	RESZ 529
ID|FBti0004135
SYM|P{hsneo}ifc<up>des</up>
ASTP|<fbsym>FBtp0000078==P{hsneo}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0001941==ifc</fbsym>
ARGS|FBgn0001941

REFDSR
{
RDID|FBrf0091054
|Endo et al.
|1996
SYN|P{hsneo}ifc<up>des</up>
ASAL|<fbsym>FBal0057253==ifc<up>des</up></fbsym>
CLOC|26B2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001941==ifc</fbsym>
PHC|male sterile | recessive
|semi-lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0091054
|Endo et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0057253==ifc<up>des</up></fbsym>

REFDSR
{
RDID|FBrf0091054
|Endo et al.
|1996
PHP|20-50% of homozygotes die during the embryonic stages.
|Female fertility is unaffected.
|Mutants testes are smaller than wild type and do not contain elongated
|spermatids. Primary spermatocytes enter the growth phase, giving rise
|to morphologically mature primary spermatocytes with normal large nuclei,
|prominent nucleoli and decondensed chromosomes. They then degenerate
|without initiating the meiotic chromosome condensation that normally
|... (see <fbsym>FBal0057253==ifc<up>des</up></fbsym> report)
PHM|testis
|spermatid
}

REF
{
REFM|FBrf0091054
|Endo et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004141	ICL 1 P	SYM 1 P{lArB}emc<up>P</up>	ASTR 1 -	CLOC 1 61C9	REF 1 2	DT 1 8 Oct 1997	RESZ 437
ID|FBti0004141
SYM|P{lArB}emc<up>P</up>
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0000575==emc</fbsym>

REFDSR
{
RDID|FBrf0090681
|Mackay and Fry
|1996
SYN|P{lArB}emc<up>P</up>
ASAL|<fbsym>FBal0057500==emc<up>P</up></fbsym>
CLOC|61C9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000575==emc</fbsym>
}

REF
{
REFM|FBrf0090681
|Mackay and Fry
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004148	ICL 1 P	SYM 1 P{lwB}afl<up>ts</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Oct 1997	RESZ 442
ID|FBti0004148
SYM|P{lwB}afl<up>ts</up>
ASTP|<fbsym>FBtp0000157==P{lwB}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0019909==afl</fbsym>

REFDSR
{
RDID|FBrf0091451
|Sur et al.
|1996
SYN|P{lwB}afl<up>ts</up>
ASAL|<fbsym>FBal0057939==afl<up>ts</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0019909==afl</fbsym>
PHC|lethal | recessive | conditional ts
}

REF
{
REFM|FBrf0091451
|Sur et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0057939==afl<up>ts</up></fbsym>

REFDSR
{
RDID|FBrf0091451
|Sur et al.
|1996
PHP|Most homozygotes die as embryos or larvae, viability of homozygous
|females is always lower then that of homozygous males. Rare escapers
|are semi-sterile but morphologically normal.
}

REF
{
REFM|FBrf0091451
|Sur et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004228	ICL 1 P	SYM 1 P{lacW}nej<up>P</up>	ASTR 1 -	CLOC 1 8F7--9	REF 1 4	DT 1 8 Oct 1997	RESZ 901
ID|FBti0004228
SYM|P{lacW}nej<up>P</up>
SYN|p<up>w<up>+</up></up><up>nej</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0015624==nej</fbsym>
SK|FBst0003728
|w[*] P{w[+mC]=lacW}nej[P]/FM7c
|Total=1

REFDSR
{
RDID|FBrf0093058
|Akimaru et al.
|1997
SYN|P{lacW}nej<up>P</up>
ASAL|<fbsym>FBal0059991==nej<up>P</up></fbsym>
CLOC|8F7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0015624==nej</fbsym>
}

REFDSR
{
RDID|FBrf0138518
|Kiger et al.
|2001
SYN|p<up>w<up>+</up></up><up>nej</up>
}

REFDSR
{
RDID|FBrf0180303
|Kumar et al.
|2004
PHC|(with nej<up>3</up>) lethal
|(with nej<up>Q7</up>) lethal
|(with nej<up>S103</up>) lethal
|(with nej<up>S342</up>) lethal
|(with nej<up>TA57</up>) lethal
}

REF
{
REFM|FBrf0093058
|Akimaru et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0138518
|Kiger et al.
|2001
REFM|FBrf0180303
|Kumar et al.
|2004
}

ALESR
{
ASYM|<fbsym>FBal0059991==nej<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0180303
|Kumar et al.
|2004
PHP|The <fbsym>FBal0059991==nej<up>P</up></fbsym>/<fbsym>FBal0094382==nej<up>TC41</up></fbsym> and
| <fbsym>FBal0059991==nej<up>P</up></fbsym>/<fbsym>FBal0175574==nej<up>131</up></fbsym> combinations give
|viable adults with moderately rough eyes. The ommatidia have variable
|numbers of photoreceptor cells in
| <fbsym>FBal0059991==nej<up>P</up></fbsym>/<fbsym>FBal0175574==nej<up>131</up></fbsym> adults.
PHM|(with nej<up>TC41</up>) eye
|(with nej<up>TC41</up>) ommatidium
|(with nej<up>131</up>) eye
|(with nej<up>131</up>) ommatidium
|(with nej<up>131</up>) photoreceptor cell
}

REF
{
REFM|FBrf0180303
|Kumar et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0004290	ICL 1 P	SYM 1 P{lacW}III-P	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Oct 1997	RESZ 438
ID|FBti0004290
SYM|P{lacW}III-P
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 Oct 1997
|8 Oct 1997
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0084765
|Bhojwani et al.
|1995
SYN|P{lacW}III-P
ASAL|<fbsym>FBal0061069==Ecol\lacZ<up>wg-III-P</up></fbsym>
|<fbsym>FBal0060826==w<up>wg-III-P</up></fbsym>
}

REF
{
REFM|FBrf0084765
|Bhojwani et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004773	ICL 1 P	SYM 1 P{UAS-hh.A}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 10 May 1999	RESZ 350
ID|FBti0004773
SYM|P{UAS-hh.A}III
SYN|P{UAS-hh.A1}III
|P{UAShh.1}III
ASTP|<fbsym>FBtp0001373==P{UAS-hh.A}</fbsym>
DT|10 May 1999
|29 Dec 1997
ICL|P

REFDSR
{
RDID|FBrf0098056
|Frasch
|1997.7.23
SYN|P{UAShh.1}III
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0098056
|Frasch
|1997.7.23
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0004774	ICL 1 P	SYM 1 P{GawB}rhl	ASTR 1 -	CLOC 1 62A2	REF 1 3	DT 1 29 Dec 1997	RESZ 604
ID|FBti0004774
SYM|P{GawB}rhl
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|29 Dec 1997
|29 Dec 1997
ICL|P
ASGN|<fbsym>FBgn0004635==rho</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0086318
|Axelrod et al.
|1996
ASAL|<fbsym>FBal0083445==Scer\GAL4<up>rho-rhl</up></fbsym>
}

REFDSR
{
RDID|FBrf0099060
|Noll
|1997.12.3
CLOC|62A2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004635==rho</fbsym>
CH|binary enhancer trap | <fbsym>FBgn0004635==rho</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0086318
|Axelrod et al.
|1996
REFM|FBrf0099060
|Noll
|1997.12.3
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0005135	ICL 1 P	SYM 1 P{hsneo}rt<up>P</up>	ASTR 1 -	CLOC 1 68C1-68C8	REF 1 6	DT 1 31 Jan 1998	RESZ 1152
ID|FBti0005135
SYM|P{hsneo}rt<up>P</up>
SYN|fs(3)neo1
ASTP|<fbsym>FBtp0000078==P{hsneo}</fbsym>
DT|31 Jan 1998
|3 Jan 1998
ICL|P
ID2|FBti0000118
ASGN|<fbsym>FBgn0003292==rt</fbsym>
SK|FBst0010060
|mwh[1] P{hsneo}rt[P] red[1] e[1]/TM3, Sb[1] Ser[1]
|Total=1

REFDSR
{
RDID|FBrf0049003
|Cooley et al.
|1988
SYN|P{hsneo}rt<up>P</up>
ASAL|<fbsym>FBal0014813==rt<up>P</up></fbsym>
CLOC|68C1-68C8
|Insertion site 
LOCB|in situ
}

REFDSR
{
RDID|FBrf0067338
|BDGP Project Members
|1994-1999
CLOC|68C1-68C8
|Insertion site 
LOCB|in situ
DBAF|AQ025579.1 Dual_flanking_Example.JPG
}

REFDSR
{
RDID|FBrf0111489
|Spradling et al.
|1999
PHC|female sterile | recessive
}

REFDSR
{
RDID|FBrf0184339
|FlyBase
|2005
CC|Location 3L:622835-622836 confirmed by FlyBase alignment of dbGSS accession
| AQ025579 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b.
| Insertion orientation confirmed.
}

REF
{
REFM|FBrf0049003
|Cooley et al.
|1988
REFM|FBrf0067338
|BDGP Project Members
|1994-1999
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111489
|Spradling et al.
|1999
REFM|FBrf0184339
|FlyBase
|2005
}

ALESR
{
ASYM|<fbsym>FBal0014813==rt<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0049003
|Cooley et al.
|1988
PHP|Homozygous males and females have reduced fertility and show
|abdominal rotation.
PHM|adult abdomen
}

REFDSR
{
RDID|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
PHP|The bodies of first instar larvae are rotated around the long axis,
|forcing the animals to move in a clockwise circle as they crawl. The
|larval cuticle presents a perfect segmental alignment of landmarks
|but the adult abdominal cuticle segments appear staggered relative
|to each other.
PHM|adult cuticle
}

REF
{
REFM|FBrf0049003
|Cooley et al.
|1988
REFM|FBrf0088507
|Martin-Blanco and Garcia-Bellido
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0005676	ICL 1 P	SYM 1 P{lArB}Dl<up>EW</up>	ASTR 1 -	CLOC 1 92A1--2	REF 1 2	DT 1 3 Jan 1998	RESZ 438
ID|FBti0005676
SYM|P{lArB}Dl<up>EW</up>
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|3 Jan 1998
|3 Jan 1998
ICL|P
ASGN|<fbsym>FBgn0000463==Dl</fbsym>

REFDSR
{
RDID|FBrf0098270
|Huppert et al.
|1997
SYN|P{lArB}Dl<up>EW</up>
ASAL|<fbsym>FBal0038738==Dl<up>EW</up></fbsym>
CLOC|92A1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000463==Dl</fbsym>
}

REF
{
REFM|FBrf0098270
|Huppert et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0038738==Dl<up>EW</up></fbsym>

REFDSR
{
RDID|FBrf0098270
|Huppert et al.
|1997
PHP|Wing veins are extremely thickened - all cells within the provein adopt
|the vein cell fate.
PHM|wing vein
|eye
}

REF
{
REFM|FBrf0098270
|Huppert et al.
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0007116	ICL 1 P	SYM 1 P{lacW}Lam<up>P</up>	ASTR 1 -	CLOC 1 25E6	REF 1 3	DT 1 3 Jan 1998	RESZ 641
ID|FBti0007116
SYM|P{lacW}Lam<up>P</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|3 Jan 1998
|3 Jan 1998
ICL|P
ASGN|<fbsym>FBgn0002525==Lam</fbsym>

REFDSR
{
RDID|FBrf0083257
|Lenz et al.
|1995
PHC|sterile
|semi-lethal
}

REFDSR
{
RDID|FBrf0093570
|Lenz-Bohme et al.
|1997
SYN|P{lacW}Lam<up>P</up>
ASAL|<fbsym>FBal0065070==Lam<up>P</up></fbsym>
CLOC|25E6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002525==Lam</fbsym>
PHC|male sterile | recessive
|female sterile | recessive
|lethal | recessive | partially
}

REF
{
REFM|FBrf0083257
|Lenz et al.
|1995
REFM|FBrf0093570
|Lenz-Bohme et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0065070==Lam<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0083257
|Lenz et al.
|1995
PHP|The few surviving adults show reduced viability combined with locomotion
|ataxy. They cannot fly and walking is difficult. Males and females
|are sterile.
}

REFDSR
{
RDID|FBrf0093570
|Lenz-Bohme et al.
|1997
PHP|Homozygotes have a prolonged developmental time course, with a delay
|of up to 3 days at 24<up>o</up>C. Only 5-10% of homozygotes survive until
|adulthood, with survival rate being inversely correlated with population
|density. There are three major periods of homozygous lethality; including
|the embryonic stages (20-30% lethality), the pupal stages (50-60% lethality),
|and the eclosion of the adult fly (5-10% lethality). Adults die within
|two weeks of eclosion.
|... (see <fbsym>FBal0065070==Lam<up>P</up></fbsym> report)
PHM|ovary
|ovariole
|oocyte
|spermatozoon
|nuclear pore
|annulate lamellae
|nuclear membrane
}

REF
{
REFM|FBrf0083257
|Lenz et al.
|1995
REFM|FBrf0093570
|Lenz-Bohme et al.
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009066	ICL 1 P	SYM 1 P{lacZ}ex<up>brl</up>	ASTR 1 -	CLOC 1 21C2	REF 1 2	DT 1 7 May 1998	RESZ 466
ID|FBti0009066
SYM|P{lacZ}ex<up>brl</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0004583==ex</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{lacZ}ex<up>brl</up>
ASAL|<fbsym>FBal0003908==ex<up>brl</up></fbsym>
MU|P-element activity
CLOC|21C2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004583==ex</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003908==ex<up>brl</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Strongest phenotypes include partial to full transformation of one or
|both eyes into antennae. Less severe adult phenotypes include excess
|bristles under the eyes, duplication of the more anterior set of scutellar
|bristles and a spoon-like curvature of the wings.
|Shows complete penetrance and variable expressivity.
PHM|eye
|vibrissae
|anterior scutellar bristle
|wing
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009103	ICL 1 P	SYM 1 P{lacZ}sn<up>unspecified</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 4	DT 1 7 May 1998	RESZ 660
ID|FBti0009103
SYM|P{lacZ}sn<up>unspecified</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0030136
|Mohler
|1977
PHC|female sterile | recessive
|lethal | embryonic stage | maternal effect | recessive
}

REFDSR
{
RDID|FBrf0065495
|Misra et al.
|1993
SYN|P{lacZ}sn<up>unspecified</up>
ASAL|<fbsym>FBal0035639==sn<up>unspecified</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0030136
|Mohler
|1977
REFM|FBrf0065495
|Misra et al.
|1993
REFM|FBrf0091172
|Simmons et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035639==sn<up>unspecified</up></fbsym>

REFDSR
{
RDID|FBrf0030136
|Mohler
|1977
PHP|Homozygous females lay eggs with abnormal dorsal appendages that fail
|to hatch.
PHM|dorsal appendage
|egg | maternal effect
}

REF
{
REFM|FBrf0030136
|Mohler
|1977
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009109	ICL 1 P	SYM 1 P{lacZ}trh<up>ET</up>	ASTR 1 -	CLOC 1 61C1	REF 1 2	DT 1 7 May 1998	RESZ 467
ID|FBti0009109
SYM|P{lacZ}trh<up>ET</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0003749==trh</fbsym>

REFDSR
{
RDID|FBrf0078709
|Issac and Andrew
|1995
SYN|P{lacZ}trh<up>ET</up>
ASAL|<fbsym>FBal0035844==trh<up>ET</up></fbsym>
CLOC|61C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003749==trh</fbsym>
PHC|lethal | recessive
}

REF
{
REFM|FBrf0078709
|Issac and Andrew
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035844==trh<up>ET</up></fbsym>

REFDSR
{
RDID|FBrf0078709
|Issac and Andrew
|1995
PHP|Trachea are absent, filzkorper fail to elongate. Salivary duct cells
|fail to invaginate to form tubes.
PHM|trachea
|filzkorper
|larval salivary gland duct & embryo
}

REF
{
REFM|FBrf0078709
|Issac and Andrew
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009111	ICL 1 P	SYM 1 P{lacZ}vas<up>unspecified</up>	ASTR 1 -	CLOC 1 35B10--C1	REF 1 4	DT 1 7 May 1998	RESZ 790
ID|FBti0009111
SYM|P{lacZ}vas<up>unspecified</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0003970==vas</fbsym>

REFDSR
{
RDID|FBrf0049878
|Schupbach and Wieschaus
|1989
PHC|female sterile | recessive
|lethal | embryonic stage | recessive | maternal effect
}

REFDSR
{
RDID|FBrf0051973
|Ashburner et al.
|1990
PHC|lethal | maternal effect
}

REFDSR
{
RDID|FBrf0091172
|Simmons et al.
|1996
SYN|P{lacZ}vas<up>unspecified</up>
ASAL|<fbsym>FBal0035897==vas<up>unspecified</up></fbsym>
CLOC|35B10--C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003970==vas</fbsym>
}

REF
{
REFM|FBrf0049878
|Schupbach and Wieschaus
|1989
REFM|FBrf0051973
|Ashburner et al.
|1990
REFM|FBrf0091172
|Simmons et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035897==vas<up>unspecified</up></fbsym>

REFDSR
{
RDID|FBrf0045941
|Tearle and Nusslein-Volhard
|1987
PHP|Embryos derived from <fbsym>FBal0035897==vas<up>unspecified</up></fbsym> mutant females
| lack pole cells,
|pole plasm and abdominal segments. Eggs are also an abnormal shape.
PHM|pole cell
|pole plasm
|egg
|embryonic abdominal segment 1
|embryonic abdominal segment 2
|embryonic abdominal segment 3
|embryonic abdominal segment 4
|embryonic abdominal segment 5
|embryonic abdominal segment 6
|embryonic abdominal segment 7
|embryonic abdominal segment 8
|embryonic abdominal segment 9
|embryonic abdominal segment 10
|embryonic abdominal segment 11
}

REFDSR
{
RDID|FBrf0049878
|Schupbach and Wieschaus
|1989
PHP|Eggs derived from homozygous females show a "grandchildless knirps-like"
|phenotype; they lack polar granules and pole cells and show deletions
|of abdominal segments similar to that seen in <fbsym>FBgn0001320==kni</fbsym> mutant embryos.
PHM|pole granule | maternal effect
|pole cell | maternal effect
|embryonic abdominal segment | maternal effect
}

REFDSR
{
RDID|FBrf0104438
|Ghabrial et al.
|1998
PHP|Condensation of DNA in the oocyte nucleus to form the karyosome is
|abnormal in homozygous egg chambers. In some cases the DNA is more
|diffuse than normal or it is threadlike and fragmented.
PHM|karyosome
}

REFDSR
{
RDID|FBrf0111879
|Ghabrial and Schupbach
|1999
PHM|karyosome
}

REF
{
REFM|FBrf0045941
|Tearle and Nusslein-Volhard
|1987
REFM|FBrf0049878
|Schupbach and Wieschaus
|1989
REFM|FBrf0104438
|Ghabrial et al.
|1998
REFM|FBrf0111879
|Ghabrial and Schupbach
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009112	ICL 1 P	SYM 1 P{lacZ}wg<up>et</up>	ASTR 1 -	CLOC 1 27F1	REF 1 3	DT 1 7 May 1998	RESZ 631
ID|FBti0009112
SYM|P{lacZ}wg<up>et</up>
SYN|wg-lacZ
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0004009==wg</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0058091
|Cohen et al.
|1993
SYN|P{lacZ}wg<up>et</up>
ASAL|<fbsym>FBal0147926==Ecol\lacZ<up>wg-et</up></fbsym>
|<fbsym>FBal0033180==wg<up>et</up></fbsym>
CLOC|27F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004009==wg</fbsym>
}

REFDSR
{
RDID|FBrf0149132
|Ryoo et al.
|2002
SYN|wg-lacZ
}

REF
{
REFM|FBrf0058091
|Cohen et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149132
|Ryoo et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009133	ICL 1 P	SYM 1 P{lacZ}svp<up>w+</up>	ASTR 1 -	CLOC 1 87B4--5	REF 1 3	DT 1 7 May 1998	RESZ 581
ID|FBti0009133
SYM|P{lacZ}svp<up>w+</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0003651==svp</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0073371
|Hoshizaki et al.
|1994
SYN|P{lacZ}svp<up>w+</up>
ASAL|<fbsym>FBal0041986==Ecol\lacZ<up>svp-w+</up></fbsym>
|<fbsym>FBal0040005==svp<up>w+</up></fbsym>
CLOC|87B4--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003651==svp</fbsym>
}

REF
{
REFM|FBrf0073371
|Hoshizaki et al.
|1994
REFM|FBrf0083200
|Hoshizaki et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009494	ICL 1 P	SYM 1 P{lacZ}SGT	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 7 May 1998	RESZ 356
ID|FBti0009494
SYM|P{lacZ}SGT
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0093054
|Bradley and Andrew
|1997
SYN|P{lacZ}SGT
ASAL|<fbsym>FBal0060278==Ecol\lacZ<up>SGT</up></fbsym>
}

REF
{
REFM|FBrf0093054
|Bradley and Andrew
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009562	ICL 1 P	SYM 1 P{lacZ}N<up>MLz</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 5	DT 1 31 Jan 2002	RESZ 1033
ID|FBti0009562
SYM|P{lacZ}N<up>MLz</up>
SYN|N-lacZ
|P<up>lacZ</up>N<up>MLz</up>
|P{lacZ}MLz
|P{lacZ}N<up>MLz</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|31 Jan 2002
|7 May 1998
ICL|P
ID2|FBti0009498
ASGN|<fbsym>FBgn0004647==N</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0092741
|de Celis
|1997
SYN|P{lacZ}MLz
ASAL|<fbsym>FBal0060283==Ecol\lacZ<up>N-MLz</up></fbsym>
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REFDSR
{
RDID|FBrf0093808
|de Celis et al.
|1997
SYN|P{lacZ}N<up>MLz</up>
ASAL|<fbsym>FBal0061710==N<up>MLz</up></fbsym>
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REFDSR
{
RDID|FBrf0144791
|Pavlopoulos et al.
|2001
SYN|N-lacZ
|P<up>lacZ</up>N<up>MLz</up>
}

REFDSR
{
RDID|FBrf0180171
|Hori et al.
|2004
SYN|N-lacZ
}

REF
{
REFM|FBrf0092741
|de Celis
|1997
REFM|FBrf0093808
|de Celis et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0144791
|Pavlopoulos et al.
|2001
REFM|FBrf0180171
|Hori et al.
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009579	ICL 1 P	SYM 1 P{lacZ}egr	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 7 May 1998	RESZ 346
ID|FBti0009579
SYM|P{lacZ}egr
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0064552
|Kojima et al.
|1993
SYN|P{lacZ}egr
ASAL|<fbsym>FBal0062619==Ecol\lacZ<up>egr</up></fbsym>
}

REF
{
REFM|FBrf0064552
|Kojima et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009597	ICL 1 P	SYM 1 P{lacZ}SC	ASTR 1 -	CLOC 1 -	REF 1 3	DT 1 7 May 1998	RESZ 408
ID|FBti0009597
SYM|P{lacZ}SC
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0053789
|Stuttem and Campos-Ortega
|1991
SYN|P{lacZ}SC
ASAL|<fbsym>FBal0063958==Ecol\lacZ<up>SC</up></fbsym>
}

REF
{
REFM|FBrf0053789
|Stuttem and Campos-Ortega
|1991
REFM|FBrf0055867
|Luer and Technau
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009734	ICL 1 P	SYM 1 P{lacZ}RBG	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 7 May 1998	RESZ 350
ID|FBti0009734
SYM|P{lacZ}RBG
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0078208
|Choi and Benzer
|1993
SYN|P{lacZ}RBG
ASAL|<fbsym>FBal0082641==Ecol\lacZ<up>RBG</up></fbsym>
}

REF
{
REFM|FBrf0078208
|Choi and Benzer
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0009828	ICL 1 P	SYM 1 P{lacW}colt<up>P</up>	ASTR 1 -	CLOC 1 23A5	REF 1 2	DT 1 7 May 1998	RESZ 668
ID|FBti0009828
SYM|P{lacW}colt<up>P</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|7 May 1998
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0019830==colt</fbsym>
ARGS|FBgn0019830

REFDSR
{
RDID|FBrf0099765
|Hartenstein et al.
|1997
SYN|P{lacW}colt<up>P</up>
ASAL|<fbsym>FBal0083032==colt<up>P</up></fbsym>
CLOC|23A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0019830==colt</fbsym>
PHC|female sterile | poor
|semi-lethal | recessive
CC|Orientation of <fbsym>FBtp0000204==P{lacW}</fbsym> element is 5' to 3' relative to transcription (5'
| to 3') of <fbsym>FBgn0019830==colt</fbsym>.
}

REF
{
REFM|FBrf0099765
|Hartenstein et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0083032==colt<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0099765
|Hartenstein et al.
|1997
PHP|Mutation causes semi-lethality with death of a high proportion of first
|instar larvae, allowing 20% of mutants to emerge from the pupal case.
|Adult escapers are characterized by partially unfolded wings with
|loss of venation and reduced size (more in their width than their length).
|Wing phenotype may vary from nearly normal wings to warped wings with
|a rough texture reflecting a higher density of trichomes. Escapers
|also exhibit poor viability and sterility, 25% of females give rise
|... (see <fbsym>FBal0083032==colt<up>P</up></fbsym> report)
PHM|embryonic/larval tracheal system
|wing
|wing vein
|wing & trichome
}

REF
{
REFM|FBrf0099765
|Hartenstein et al.
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0009829	ICL 1 P	SYM 1 P{lacW}pum<up>bem</up>	ASTR 1 -	CLOC 1 85C4--D1	REF 1 2	DT 1 14 Oct 2001	RESZ 525
ID|FBti0009829
SYM|P{lacW}pum<up>bem</up>
SYN|P{lacW}bem<up>1</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|14 Oct 2001
|7 May 1998
ICL|P
ASGN|<fbsym>FBgn0003165==pum</fbsym>
SK|FBst0006782
|w[*]; P{w[+mC]=lacW}pum[bem]/TM6
|Total=1

REFDSR
{
RDID|FBrf0085988
|Stern et al.
|1995
SYN|P{lacW}bem<up>1</up>
ASAL|<fbsym>FBal0083062==pum<up>bem</up></fbsym>
CLOC|85C4--D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003165==pum</fbsym>
}

REF
{
REFM|FBrf0085988
|Stern et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0083062==pum<up>bem</up></fbsym>

REFDSR
{
RDID|FBrf0085988
|Stern et al.
|1995
PHP|Flies exhibit greatly reduced coordination, flight ability and fertility.
|Mutation affects synaptic transmission at the larval neuromuscular
|junction via an affect on excitability in the motor neuron: the mutation
|acts presynaptically to cause increased transmitter release. Larvae
|exhibit a more rapid onset of augmentation than <fbsym>FBgn0003165==pum</fbsym><up>+</up> larvae.
PHM|neuromuscular junction
}

REFDSR
{
RDID|FBrf0151333
|Schweers et al.
|2002
PHP|<fbsym>FBal0083062==pum<up>bem</up></fbsym>/<fbsym>FBal0014078==pum<up>7</up></fbsym> and
| <fbsym>FBal0083062==pum<up>bem</up></fbsym>/<fbsym>FBal0014080==pum<up>9</up></fbsym>
| transheterozygotes exhibit
|a significantly faster long term facilitation (LTF) at the neuromuscular
|junction than seen in wild-type. Larvae also respond to nerve stimuli
|with excitatory junctional potentials (ejp's) about 95% of time
|(as compared to about 80% in controls) in low Ca<up>2+</up> (0.15mM) conditions.
|At 0.10mM Ca<up>2+</up> an ejp response is seen about 85% of the time (as
|compared to about 35% in controls).
}

REF
{
REFM|FBrf0085988
|Stern et al.
|1995
REFM|FBrf0151333
|Schweers et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0010381	ICL 1 P	SYM 1 P{lArB}chsB	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 19 Jun 1998	RESZ 339
ID|FBti0010381
SYM|P{lArB}chsB
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|19 Jun 1998
|19 Jun 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0100917
|Siddiqi
|1998
SYN|P{lArB}chsB
ASAL|<fbsym>FBal0088974==Ecol\lacZ<up>chsB</up></fbsym>
}

REF
{
REFM|FBrf0100917
|Siddiqi
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0010382	ICL 1 P	SYM 1 P{lArB}chsA	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 19 Jun 1998	RESZ 339
ID|FBti0010382
SYM|P{lArB}chsA
ASTP|<fbsym>FBtp0000160==P{lArB}</fbsym>
DT|19 Jun 1998
|19 Jun 1998
ICL|P
ASGN|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0100917
|Siddiqi
|1998
SYN|P{lArB}chsA
ASAL|<fbsym>FBal0088975==Ecol\lacZ<up>chsA</up></fbsym>
}

REF
{
REFM|FBrf0100917
|Siddiqi
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0010665	ICL 1 P	SYM 1 P{lacW}T's	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 26 Aug 1998	RESZ 347
ID|FBti0010665
SYM|P{lacW}T's
SYN|P{lacW}T's
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
SYN|P{lacW}T's
ASAL|<fbsym>FBal0090054==w<up>T's</up></fbsym>
}

REF
{
REFM|FBrf0102846
|Netter et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0090054==w<up>T's</up></fbsym>

REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
PHP|Pigmented area corresponds to dorsal half of the eye, with a pigmentation
|level ranging from orange to red. Ventral section of eye is white.
PHM|pigment cell
}

REF
{
REFM|FBrf0102846
|Netter et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0010674	ICL 1 P	SYM 1 P{lacW}moz<up>UK</up>	ASTR 1 -	CLOC 1 21--60	REF 1 2	DT 1 26 Aug 1998	RESZ 475
ID|FBti0010674
SYM|P{lacW}moz<up>UK</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|<fbsym>FBgn0024853==moz</fbsym>

REFDSR
{
RDID|FBrf0102829
|Fabrizio et al.
|1998
SYN|P{lacW}moz<up>UK</up>
ASAL|<fbsym>FBal0090221==moz<up>UK</up></fbsym>
CLOC|21--60
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0024853==moz</fbsym>
PHC|male sterile | recessive
}

REF
{
REFM|FBrf0102829
|Fabrizio et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0090221==moz<up>UK</up></fbsym>

REFDSR
{
RDID|FBrf0102829
|Fabrizio et al.
|1998
PHP|Mutants show male sterility, with highly elongated, immobile, blebbed
|sperm tails and abnormal nuclear morphology. Nuclei are incompletely
|condensed and irregularly shaped. Construction of an individualization
|complex is attempted.
PHM|spermatozoon
|primary spermatocyte cyst
|spermatid & nucleus
}

REF
{
REFM|FBrf0102829
|Fabrizio et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0010693	ICL 1 P	SYM 1 P{PZ}amn<up>chpd</up>	ASTR 1 -	CLOC 1 18F4--19A2	REF 1 2	DT 1 26 Aug 1998	RESZ 444
ID|FBti0010693
SYM|P{PZ}amn<up>chpd</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|26 Aug 1998
|26 Aug 1998
ICL|P
ASGN|<fbsym>FBgn0000076==amn</fbsym>

REFDSR
{
RDID|FBrf0102808
|Moore et al.
|1998
SYN|P{PZ}amn<up>chpd</up>
ASAL|<fbsym>FBal0090484==amn<up>chpd</up></fbsym>
CLOC|18F4--19A2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000076==amn</fbsym>
}

REF
{
REFM|FBrf0102808
|Moore et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0090484==amn<up>chpd</up></fbsym>

REFDSR
{
RDID|FBrf0102808
|Moore et al.
|1998
PHP|Hemizygous males and homozygous females show increased sensitivity
|to ethanol; they elute from an inebriometer with a mean elution time
|(MET) of approximately 15 minutes compared with an MET of 20 minutes
|for wild-type controls.
|<fbsym>FBal0090484==amn<up>chpd</up></fbsym> flies show normal geotaxis and locomotor
| activity. Ethanol
|absorption and metabolism is normal in these flies.
|The ethanol-sensitive phenotype is reversed by treatment of the flies
|... (see <fbsym>FBal0090484==amn<up>chpd</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0155893 
PHP|<fbsym>FBal0090484==amn<up>chpd</up></fbsym> mutant flies show similar response profiles
| to wild-type
|flies in response to ethanol: flies have an initial startle response,
|a brief moment of quiescence followed by a sustained period of hyperactivity
|and a reduction in locomotor speed leading to eventual immobility.
|However, the <fbsym>FBal0090484==amn<up>chpd</up></fbsym> mutants have a more intense
| hyperactive phase
|and reach maximal hyperactivity more quickly, leading to a faster onset
|of immobility. During the hyperactive phase, <fbsym>FBal0090484==amn<up>chpd</up></fbsym>
| mutants initiate
|... (see <fbsym>FBal0090484==amn<up>chpd</up></fbsym> report)
}

REF
{
REFM|FBrf0102808
|Moore et al.
|1998
REFM|FBrf0155893 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012414	ICL 1 P	SYM 1 P{GMR-rpr.H}M	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 10 May 1999	RESZ 362
ID|FBti0012414
SYM|P{GMR-rpr.H}M
SYN|GMR-rprM
ASTP|<fbsym>FBtp0001630==P{GMR-rpr.H}</fbsym>
DT|10 May 1999
|8 Jan 1999
ICL|P

REFDSR
{
RDID|FBrf0085196
|Hay et al.
|1995
SYN|GMR-rprM
CC|Produces a moderate reduction in eye size (in <fbsym>FBgn0004618==gl</fbsym><up>+</up> animals).
}

REF
{
REFM|FBrf0085196
|Hay et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0012415	ICL 1 P	SYM 1 P{GMR-rpr.H}S	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 10 May 1999	RESZ 418
ID|FBti0012415
SYM|P{GMR-rpr.H}S
SYN|GMR-rprS
ASTP|<fbsym>FBtp0001630==P{GMR-rpr.H}</fbsym>
DT|10 May 1999
|8 Jan 1999
ICL|P
SK|FBst0005773
|P{w[+mC]=GMR-rpr.H}S/TM6B, Tb[+]
|Total=1

REFDSR
{
RDID|FBrf0085196
|Hay et al.
|1995
SYN|GMR-rprS
CC|Produces a severe reduction in eye size (in <fbsym>FBgn0004618==gl</fbsym><up>+</up> animals).
}

REF
{
REFM|FBrf0085196
|Hay et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0012420	ICL 1 P	SYM 1 P{hsneo}chic<up>neo</up>	ASTR 1 -	CLOC 1 26A5--B2	REF 1 3	DT 1 9 May 1999	RESZ 611
ID|FBti0012420
SYM|P{hsneo}chic<up>neo</up>
SYN|P{hsneo}chi<up>neo</up>
ASTP|<fbsym>FBtp0000078==P{hsneo}</fbsym>
DT|9 May 1999
|9 Jan 1999
ICL|P
ID2|FBti0012249
ASGN|<fbsym>FBgn0000308==chic</fbsym>
ARGS|FBgn0000308

REFDSR
{
RDID|FBrf0055547
|Cooley et al.
|1992
SYN|P{hsneo}chi<up>neo</up>
|P{hsneo}chic<up>neo</up>
ASAL|<fbsym>FBal0030749==chic<up>neo</up></fbsym>
CLOC|26A5--B2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000308==chic</fbsym>
PHC|female sterile | recessive
}

REF
{
REFM|FBrf0055547
|Cooley et al.
|1992
REFM|FBrf0100564
|Giansanti et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030749==chic<up>neo</up></fbsym>

REFDSR
{
RDID|FBrf0055547
|Cooley et al.
|1992
PHP|Fully penetrant egg chamber phenotype: nurse cells fail to deliver
|all their cytoplasm to the oocyte resulting in small oocytes surrounded
|by an egg shell.
|Strong allele of <fbsym>FBgn0000308==chic</fbsym>.
PHM|nurse cell
}

REF
{
REFM|FBrf0055547
|Cooley et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012460	ICL 1 M	SYM 1 M{peach}Dmau\w<up>pch</up>	ASTR 1 -	CLOC 1 3C	REF 1 16	DT 1 10 May 1999	RESZ 1035
ID|FBti0012460
SYM|M{peach}Dmau\w<up>pch</up>
SYN|w<up>pch</up>
ASTP|<fbsym>FBtp0001666==M{peach}</fbsym>
DT|10 May 1999
|4 Feb 1999
ICL|M
ASGN|<fbsym>FBgn0015655==Dmau\w</fbsym>

REFDSR
{
RDID|FBrf0047302
|Bryan et al.
|1987
SYN|w<up>pch</up>
}

REFDSR
{
RDID|FBrf0054139
|Garza et al.
|1991
ASAL|<fbsym>FBal0035990==Dmau\w<up>pch</up></fbsym>
CLOC|3C
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0015655==Dmau\w</fbsym>
}

REF
{
REFM|FBrf0045285
|Jacobson et al.
|1986
REFM|FBrf0047302
|Bryan et al.
|1987
REFM|FBrf0051913
|Bryan et al.
|1990
REFM|FBrf0053639
|Jacobson
|1991
REFM|FBrf0054139
|Garza et al.
|1991
REFM|FBrf0056227
|Capy et al.
|1992
REFM|FBrf0058610
|Lidholm et al.
|1993
REFM|FBrf0082291
|Lohe et al.
|1995
REFM|FBrf0084227
|Nikitin and Woodruff
|1995
REFM|FBrf0086524
|Lohe and Hartl
|1996
REFM|FBrf0090674
|Lohe et al.
|1996
REFM|FBrf0091100
|Kim and Moon
|1996
REFM|FBrf0092615
|Lohe et al.
|1997
REFM|FBrf0093707
|Hartl et al.
|1997
REFM|FBrf0099809
|Hartl et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035990==Dmau\w<up>pch</up></fbsym>

REFDSR
{
RDID|FBrf0051913
|Bryan et al.
|1990
PHP|Eye color: peach.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0090674
|Lohe et al.
|1996
PHP|Eye color: peach.
PHM|pigment cell
}

REF
{
REFM|FBrf0051913
|Bryan et al.
|1990
REFM|FBrf0090674
|Lohe et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012568	ICL 1 P	SYM 1 P{lacZ}hh<up>lacZ</up>	ASTR 1 -	CLOC 1 94E1	REF 1 2	DT 1 11 Mar 1999	RESZ 445
ID|FBti0012568
SYM|P{lacZ}hh<up>lacZ</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|11 Mar 1999
|11 Mar 1999
ICL|P
ASGN|<fbsym>FBgn0004644==hh</fbsym>

REFDSR
{
RDID|FBrf0105224
|Emerald and Roy
|1998
SYN|P{lacZ}hh<up>lacZ</up>
ASAL|<fbsym>FBal0094523==hh<up>lacZ</up></fbsym>
CLOC|94E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004644==hh</fbsym>
}

REF
{
REFM|FBrf0105224
|Emerald and Roy
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0094523==hh<up>lacZ</up></fbsym>

REFDSR
{
RDID|FBrf0105224
|Emerald and Roy
|1998
PHP|<fbsym>FBal0005465==hh<up>4</up></fbsym>/<fbsym>FBal0094523==hh<up>lacZ</up></fbsym> flies have
| defects in the external genitalia. In
|males, the severity of the defects can be classed into 3 types. 20%
|of males show loss of the anal plates. The typical horseshoe shape
|of the male external genitalia is maintained with a distinct lateral
|lobe, posterior lobe and claspers in these flies. In about 20% of
|males the horseshoe shape of the external genitalia is replaced with
|an "&agr;" shape, due to the absence of anal plates and a portion of the
|... (see <fbsym>FBal0094523==hh<up>lacZ</up></fbsym> report)
PHM|male genitalia
|anal plate
|genital arch
|male terminalia sensillum
|penis
|hypandrial process
|basal apodeme of penis
|gonopod thorn bristle
|gonopod long bristle
}

REF
{
REFM|FBrf0105224
|Emerald and Roy
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012584	ICL 1 P	SYM 1 P{UAS-kni.L}EP	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 30 Jun 1999	RESZ 686
ID|FBti0012584
SYM|P{UAS-kni.L}EP
ASTP|<fbsym>FBtp0002609==P{UAS-kni.L}</fbsym>
DT|30 Jun 1999
|7 May 1999
ICL|P
ASGN|<fbsym>FBgn0001320==kni</fbsym>

REFDSR
{
RDID|FBrf0104917
|Lunde et al.
|1998
ASAL|<fbsym>FBal0092912==kni<up>EP</up></fbsym>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
CC|NOT a <fbsym>FBtp0001317==P{EP}</fbsym> insertion. Expression of <fbsym>FBgn0001320==kni</fbsym> observed through-out the wing
| pouch, independent of presence of GAL4. Due to chomosomal position effect,
| since this is not observed for other insertions of <fbsym>FBtp0002609==P{UAS-kni.L}</fbsym>.
}

REF
{
REFM|FBrf0104917
|Lunde et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0012625	ICL 1 P	SYM 1 P{lacW}mog<up>p</up>	ASTR 1 -	CLOC 1 74C	REF 1 2	DT 1 8 May 1999	RESZ 438
ID|FBti0012625
SYM|P{lacW}mog<up>p</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|8 May 1999
|8 May 1999
ICL|P
ASGN|<fbsym>FBgn0026201==mog</fbsym>

REFDSR
{
RDID|FBrf0107025
|Nitasaka et al.
|1999
SYN|P{lacW}mog<up>p</up>
ASAL|<fbsym>FBal0095284==mog<up>p</up></fbsym>
CLOC|74C
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0026201==mog</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107025
|Nitasaka et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0095284==mog<up>p</up></fbsym>

REFDSR
{
RDID|FBrf0107025
|Nitasaka et al.
|1999
PHP|Flies are sensitive to UV: UV-irradiation reduces the number of
|homozygotes segregating from heterozygous stocks, and causes a
|defective eye phenotype due to somatic cell death.
|The rate of recombination in a <fbsym>FBal0095284==mog<up>p</up></fbsym> background is
| twice that
|of wild-type.
PHM|eye
}

REF
{
REFM|FBrf0107025
|Nitasaka et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012661	ICL 1 P	SYM 1 P{PZ}brk<up>XA</up>	ASTR 1 -	CLOC 1 7B1	REF 1 3	DT 1 8 May 1999	RESZ 679
ID|FBti0012661
SYM|P{PZ}brk<up>XA</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|8 May 1999
|8 May 1999
ICL|P
ASGN|<fbsym>FBgn0024250==brk</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0107636
|Campbell and Tomlinson
|1999
SYN|P{PZ}brk<up>XA</up>
ASAL|<fbsym>FBal0095493==brk<up>XA</up></fbsym>
CLOC|7B1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0024250==brk</fbsym>
PHC|lethal | pupal stage | recessive
}

REFDSR
{
RDID|FBrf0155696
|Chen and McKearin
|2003
ASAL|<fbsym>FBal0144910==Ecol\lacZ<up>brk-XA</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107636
|Campbell and Tomlinson
|1999
REFM|FBrf0155696
|Chen and McKearin
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0012680	ICL 1 copia	SYM 1 copia{}toc-BDGP	ASTR 1 -	CLOC 1 23D1--2	REF 1 2	DT 1 4 Feb 2000	RESZ 397
ID|FBti0012680
SYM|copia{}toc-BDGP
SYN|copia{}BDGP<up>1</up>
ASTP|<fbsym>FBtp0011420==copia</fbsym>
DT|4 Feb 2000
|25 Jun 1999
ICL|copia
ASGN|<fbsym>FBgn0015600==toc</fbsym>
ARGS|FBgn0015600

REFDSR
{
RDID|FBrf0104946
|FlyBase
|1996-
CLOC|23D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0015600==toc</fbsym>
}

REF
{
REFM|FBrf0104946
|FlyBase
|1996-
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0012768	ICL 1 P	SYM 1 P{HS-rho}Mod	ASTR 1 -	CLOC 1 -	REF 1 5	DT 1 30 Jun 1999	RESZ 619
ID|FBti0012768
SYM|P{HS-rho}Mod
ASTP|<fbsym>FBtp0002658==P{HS-rho}</fbsym>
DT|30 Jun 1999
|25 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0004635==rho</fbsym>

REFDSR
{
RDID|FBrf0091302
|Yu et al.
|1996
ASAL|<fbsym>FBal0035903==rho<up>Mod</up></fbsym>
CC|Insertion of <fbsym>FBtp0002658==P{HS-rho}</fbsym> that exhibits a moderate ectopic wing vein
| phenotype. Phenotype is position-specific; described as due to enhancer piracy.
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0091302
|Yu et al.
|1996
REFM|FBrf0104921
|Biehs et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035903==rho<up>Mod</up></fbsym>

REFDSR
{
RDID|FBrf0058540
|Sturtevant et al.
|1993
PHP|In the absence of heat induction individuals display a moderate constitutive
|excess vein phenotype. Homozygous phenotype is strongly suppressed
|by heterozygous <fbsym>FBal0017855==rho<up>ve-1</up></fbsym>.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0091302
|Yu et al.
|1996
PHP|One copy causes a short ectopic segment of vein between wing veins
|L3 and L4 near the margin and slight L3 and L4 deltas.
PHM|wing vein | ectopic
|wing vein L3
|wing vein L4
|wing vein
}

REFDSR
{
RDID|FBrf0104921
|Biehs et al.
|1998
PHP|Flies carrying <fbsym>FBal0035903==rho<up>Mod</up></fbsym> have ectopic wing vein material.
PHM|wing
|wing vein | ectopic
}

REFDSR
{
RDID|FBrf0108778
|Guichard et al.
|1999
PHP|Homozygous insertions cause a moderate extra-vein phenotype at 25<up>o</up>C.
PHM|wing
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0091302
|Yu et al.
|1996
REFM|FBrf0104921
|Biehs et al.
|1998
REFM|FBrf0108778
|Guichard et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012769	ICL 1 P	SYM 1 P{HS-rho}Stg	ASTR 1 -	CLOC 1 -	REF 1 6	DT 1 30 Jun 1999	RESZ 849
ID|FBti0012769
SYM|P{HS-rho}Stg
SYN|HS-rho<up>30A</up>
|Hs-rho30A
ASTP|<fbsym>FBtp0002658==P{HS-rho}</fbsym>
DT|30 Jun 1999
|25 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0004635==rho</fbsym>

REFDSR
{
RDID|FBrf0091302
|Yu et al.
|1996
ASAL|<fbsym>FBal0035904==rho<up>Stg</up></fbsym>
CC|Insertion of <fbsym>FBtp0002658==P{HS-rho}</fbsym> that exhibits a strong ectopic wing vein phenotype.
| Phenotype is position-specific; described as due to enhancer piracy.
}

REFDSR
{
RDID|FBrf0107601
|Baonza and Garcia-Bellido
|1999
SYN|Hs-rho30A
}

REFDSR
{
RDID|FBrf0152039
|Baker et al.
|2002
SYN|HS-rho<up>30A</up>
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0091302
|Yu et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107601
|Baonza and Garcia-Bellido
|1999
REFM|FBrf0152039
|Baker et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0035904==rho<up>Stg</up></fbsym>

REFDSR
{
RDID|FBrf0058540
|Sturtevant et al.
|1993
PHP|In the absence of heat induction individuals display a very strong
|constitutive excess vein phenotype.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0091302
|Yu et al.
|1996
PHP|One copy causes a strong ectopic wing vein phenotype.
PHM|wing vein | ectopic
}

REFDSR
{
RDID|FBrf0107601
|Baonza and Garcia-Bellido
|1999
PHP|<fbsym>FBal0035905==rho<up>Wk</up></fbsym>/<fbsym>FBal0035904==rho<up>Stg</up></fbsym> flies have
| extra wing veins.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0152039
|Baker et al.
|2002
PHP|Flies carrying <fbsym>FBal0035904==rho<up>Stg</up></fbsym> have wing blisters (in the
| absence of heat
|shock).
PHM|wing
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0091302
|Yu et al.
|1996
REFM|FBrf0107601
|Baonza and Garcia-Bellido
|1999
REFM|FBrf0152039
|Baker et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012782	ICL 1 P	SYM 1 P{HS-rho}Wk	ASTR 1 -	CLOC 1 -	REF 1 6	DT 1 27 Jun 1999	RESZ 781
ID|FBti0012782
SYM|P{HS-rho}Wk
SYN|HS-rho<up>27B</up>
|Hs-rho27B
|weak hs-rho
ASTP|<fbsym>FBtp0002658==P{HS-rho}</fbsym>
DT|27 Jun 1999
|27 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0004635==rho</fbsym>

REFDSR
{
RDID|FBrf0058540
|Sturtevant et al.
|1993
SYN|P{HS-rho}Wk
ASAL|<fbsym>FBal0035905==rho<up>Wk</up></fbsym>
}

REFDSR
{
RDID|FBrf0107601
|Baonza and Garcia-Bellido
|1999
SYN|Hs-rho27B
}

REFDSR
{
RDID|FBrf0108778
|Guichard et al.
|1999
SYN|weak hs-rho
}

REFDSR
{
RDID|FBrf0152039
|Baker et al.
|2002
SYN|HS-rho<up>27B</up>
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0076146
|Sturtevant and Bier
|1995
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107601
|Baonza and Garcia-Bellido
|1999
REFM|FBrf0108778
|Guichard et al.
|1999
REFM|FBrf0152039
|Baker et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0035905==rho<up>Wk</up></fbsym>

REFDSR
{
RDID|FBrf0058540
|Sturtevant et al.
|1993
PHP|In the absence of heat induction individuals display a very weak constitutive
|excess vein phenotype.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0107601
|Baonza and Garcia-Bellido
|1999
PHP|<fbsym>FBal0035905==rho<up>Wk</up></fbsym>/<fbsym>FBal0035904==rho<up>Stg</up></fbsym> flies have
| extra wing veins.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0108778
|Guichard et al.
|1999
PHP|Whether heatshocked or not, this non-inducable line exhibits a very
|weak extra wing vein phenotype.
PHM|wing vein
}

REFDSR
{
RDID|FBrf0152039
|Baker et al.
|2002
PHP|Flies carrying <fbsym>FBal0035905==rho<up>Wk</up></fbsym> have ectopic veins in the wing
| (in the absence
|of heat shock).
PHM|wing vein | ectopic
}

REF
{
REFM|FBrf0058540
|Sturtevant et al.
|1993
REFM|FBrf0107601
|Baonza and Garcia-Bellido
|1999
REFM|FBrf0108778
|Guichard et al.
|1999
REFM|FBrf0152039
|Baker et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012783	ICL 1 P	SYM 1 P{ninaE<up>+</up>}so<up>mda</up>	ASTR 1 -	CLOC 1 43B3--C1	REF 1 2	DT 1 27 Jun 1999	RESZ 506
ID|FBti0012783
SYM|P{ninaE<up>+</up>}so<up>mda</up>
ASTP|<fbsym>FBtp0002662==P{ninaE<up>+</up>}</fbsym>
DT|27 Jun 1999
|27 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0003460==so</fbsym>
ARGS|FBgn0003460

REFDSR
{
RDID|FBrf0079386
|Serikaku and O'Tousa
|1994
SYN|P{ninaE<up>+</up>}so<up>mda</up>
ASAL|<fbsym>FBal0039964==so<up>mda</up></fbsym>
CLOC|43B3--C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003460==so</fbsym>
}

REF
{
REFM|FBrf0079386
|Serikaku and O'Tousa
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0039964==so<up>mda</up></fbsym>

REFDSR
{
RDID|FBrf0079386
|Serikaku and O'Tousa
|1994
PHP|Aberrant development of the larval photoreceptor (Bolwigs) organ and
|the optic lobe primordium of the embryo. Adult photoreceptors fail
|to project axons into the optic ganglion, as a consequence optic lobe
|development is aborted and photoreceptor cells show age-dependent retinal
|degeneration and exhibit severe defects in the light evoked response.
|Peripheral regions of the eye show indentations or depressions. Heterozygotes
|with <fbsym>FBal0015924==so<up>1</up></fbsym> are wild type.
PHM|Bolwig's organ
|visual primordium
|photoreceptor cell
}

REFDSR
{
RDID|FBrf0108151
|Busto et al.
|1999
PHP|Wild-type larvae reduce their path lengths and show increased head
|swinging when exposed to light. This response is abolished in <fbsym>FBal0039964==so<up>mda</up></fbsym>
|larvae. Wild-type larvae show a greater change in direction when lights
|are turned on or off (light (L) to dark (D), or D to L transition)
|than in the absence of a light transition (D to D). The amplitude
|of change of direction is greater for the D to L than for the L to
|D transition. The difference in the amplitude of change of direction
|... (see <fbsym>FBal0039964==so<up>mda</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0129852
|Hassan et al.
|2000
PHP|Mutant larvae show no significant response to light (as measured by
|a "checker assay").
}

REFDSR
{
RDID|FBrf0144829
|Malpel et al.
|2002
PHP|Third instar larvae have detectable dendritic arborization of the lateral
|neurons in only 9% of cases.
|Optic lobes are completely missing in mutant animals and no retinal
|axons enter the brain, but eyelet cell boies and projections are present.
PHM|larval lateral neuron
|optic lobe
}

REF
{
REFM|FBrf0079386
|Serikaku and O'Tousa
|1994
REFM|FBrf0108151
|Busto et al.
|1999
REFM|FBrf0129852
|Hassan et al.
|2000
REFM|FBrf0144829
|Malpel et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012795	ICL 1 P	SYM 1 P{HS-rho}Sld	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 27 Jun 1999	RESZ 340
ID|FBti0012795
SYM|P{HS-rho}Sld
ASTP|<fbsym>FBtp0002658==P{HS-rho}</fbsym>
DT|27 Jun 1999
|27 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0004635==rho</fbsym>

REFDSR
{
RDID|FBrf0104921
|Biehs et al.
|1998
SYN|P{HS-rho}Sld
ASAL|<fbsym>FBal0092455==rho<up>Sld</up></fbsym>
}

REF
{
REFM|FBrf0104921
|Biehs et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0092455==rho<up>Sld</up></fbsym>

REFDSR
{
RDID|FBrf0104921
|Biehs et al.
|1998
PHP|Heterozygotes have intervein sectors converted into solid veins.
PHM|wing
|wing vein
}

REF
{
REFM|FBrf0104921
|Biehs et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012797	ICL 1 P	SYM 1 P{lacW}wg<up>Gla-PRev</up>	ASTR 1 -	CLOC 1 27F1	REF 1 2	DT 1 27 Jun 1999	RESZ 595
ID|FBti0012797
SYM|P{lacW}wg<up>Gla-PRev</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|27 Jun 1999
|27 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0004009==wg</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0106272
|Brunner et al.
|1999
SYN|P{lacW}wg<up>Gla-PRev</up>
ASAL|<fbsym>FBal0097270==Ecol\lacZ<up>wg-Gla-PRev</up></fbsym>
|<fbsym>FBal0096632==wg<up>Gla-PRev</up></fbsym>
CLOC|27F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004009==wg</fbsym>
PHC|lethal | segment polarity | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106272
|Brunner et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0096632==wg<up>Gla-PRev</up></fbsym>

REFDSR
{
RDID|FBrf0106272
|Brunner et al.
|1999
PHP|The eye phenotype is almost completely wild-type.
|<fbsym>FBal0096632==wg<up>Gla-PRev</up></fbsym>/<fbsym>FBal0044470==wg<up>rO216</up></fbsym> animals
| die, showing a strong segment polarity
|phenotype indistinguishable from that of <fbsym>FBal0044470==wg<up>rO216</up></fbsym> homozygotes.
PHM|segment polarity
}

REF
{
REFM|FBrf0106272
|Brunner et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0012798	ICL 1 P	SYM 1 P{PZ}und<up>P</up>	ASTR 1 -	CLOC 1 30C7	REF 1 2	DT 1 27 Jun 1999	RESZ 467
ID|FBti0012798
SYM|P{PZ}und<up>P</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|27 Jun 1999
|27 Jun 1999
ICL|P
ASGN|<fbsym>FBgn0025117==und</fbsym>

REFDSR
{
RDID|FBrf0108434
|Cutforth and Gaul
|1999
SYN|P{PZ}und<up>P</up>
ASAL|<fbsym>FBal0096639==und<up>P</up></fbsym>
CLOC|30C7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0025117==und</fbsym>
PHC|semi-lethal | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108434
|Cutforth and Gaul
|1999
}

ALESR
{
ASYM|<fbsym>FBal0096639==und<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0108434
|Cutforth and Gaul
|1999
PHP|Homozygotes have a roughened eye with a pronounced indentation at the
|anterior margin.
|In <fbsym>FBal0096639==und<up>P</up></fbsym>/<fbsym>und<up>&Dgr;19</up></fbsym> flies,
| the ommatidia occasionally have reversed
|polarity along the D/V axis. Some photoreceptor cells are missing.
PHM|eye
|wing
|eye | anterior
|ommatidium
|photoreceptor cell
}

REF
{
REFM|FBrf0108434
|Cutforth and Gaul
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013020	ICL 1 P	SYM 1 P{?'}hh<up>A</up>	ASTR 1 -	CLOC 1 94E1	REF 1 2	DT 1 14 Sep 1999	RESZ 503
ID|FBti0013020
SYM|P{?'}hh<up>A</up>
SYN|P{?'}hh<up>A</up>
ASTP|<fbsym>FBtp0002762==P{?'}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|P
ASGN|<fbsym>FBgn0004644==hh</fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
SYN|P{?'}hh<up>A</up>
ASAL|<fbsym>FBal0031480==hh<up>A</up></fbsym>
CLOC|94E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004644==hh</fbsym>
PHC|lethal | recessive
|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031480==hh<up>A</up></fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
PHP|Mild hh cuticle phenotype when heterozygous with
| <fbsym>FBal0005470==hh<up>9</up></fbsym>, or when homozygous,
|with occasional abdominal and thoracic denticle belt fusions. When
|heterozygous with <fbsym>FBal0005465==hh<up>4</up></fbsym>, at 18<up>o</up>C, some adults
| are produced, with wild
|type eyes. Eyes wild type over <fbsym>FBal0031487==hh<up>bar3</up></fbsym>.
|Homozygous embryos exhibit occasional abdominal and thoracic denticle
|belt fusions. Lethal when in homozygous or heterozygous combination
|with <fbsym>FBal0005466==hh<up>5</up></fbsym>, <fbsym>FBal0005469==hh<up>8</up></fbsym> or
| <fbsym>FBal0005470==hh<up>9</up></fbsym>. Transheterozygotes with <fbsym>FBal0005465==hh<up>4</up></fbsym>
|... (see <fbsym>FBal0031480==hh<up>A</up></fbsym> report)
PHM|denticle belt
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013021	ICL 1 P	SYM 1 P{?'}hh<up>AC</up>	ASTR 1 -	CLOC 1 94E1	REF 1 3	DT 1 14 Sep 1999	RESZ 661
ID|FBti0013021
SYM|P{?'}hh<up>AC</up>
SYN|P{?'}hh<up>AC</up>
ASTP|<fbsym>FBtp0002762==P{?'}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|P
ASGN|<fbsym>FBgn0004644==hh</fbsym>
SK|FBst0001749
|ry[506] hh[AC]/TM3, Sb[1]
|Total=1

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
SYN|P{?'}hh<up>AC</up>
ASAL|<fbsym>FBal0031481==hh<up>AC</up></fbsym>
CLOC|94E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004644==hh</fbsym>
PHC|lethal | recessive
|lethal | embryonic stage | recessive
}

REFDSR
{
RDID|FBrf0087580
|Ma et al.
|1996
PHC|lethal | recessive
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
REFM|FBrf0087580
|Ma et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031481==hh<up>AC</up></fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
PHP|Extreme hh cuticle phenotype when heterozygous with
| <fbsym>FBal0005470==hh<up>9</up></fbsym>, or when
|homozygous. Head segments fail to involute, naked cuticle portion
|of segment lost causing half size embryos with a lawn of denticles.
|When heterozygous with <fbsym>FBal0005465==hh<up>4</up></fbsym> at 18<up>o</up>C, adults
| show extreme mutant
|eye phenotype, also seen when heterozygous with <fbsym>FBal0031487==hh<up>bar3</up></fbsym>.
|Homozygous embryos exhibit failure head involution and loss of naked
|cuticle from the posterior surface of each segment. Lethal when in
|... (see <fbsym>FBal0031481==hh<up>AC</up></fbsym> report)
PHM|embryonic head
|denticle belt
}

REFDSR
{
RDID|FBrf0064592
|Ma et al.
|1993
PHP|Small clones of this allele in the eye have no effect, large clones
|have a non-cell autonomous disrupting effect on the array of rows and
|columns of the ommatidia, fused ommatidia and (rarely) loss of retinal
|tissue. Strong enhancer of <fbsym>FBal0005042==gl<up>3</up></fbsym>.
}

REFDSR
{
RDID|FBrf0091006
|Andrew et al.
|1997
PHP|Double mutant phenotype with <fbsym>FBgn0004396==CrebA</fbsym> mutants is additive.
}

REFDSR
{
RDID|FBrf0098358
|Strutt and Mlodzik
|1997
PHP|Clones in the developing eye cause no effect on the progression of
|the furrow other than a very subtle retardation, even when the clones
|are large.
}

REFDSR
{
RDID|FBrf0099759
|Dominguez and Hafen
|1997
PHP|Clones situated entirely within the eye field do not affect morphogenetic
|furrow propogation or ommatidial differentiation. Only in the center
|of large clones is the progression of the morphogenetic furrow retarded
|relative to the adjacent tissue. <fbsym>FBgn0004644==hh</fbsym> secreted from the neighboring
|wild type ommatidia rescues, in a nonautonomous manner, loss of <fbsym>FBgn0004644==hh</fbsym>.
|Clones that span the lateral or posterior margin of the eye exhibit
|no neuronal differentiation. Marginal clones lead to the formation
|... (see <fbsym>FBal0031481==hh<up>AC</up></fbsym> report)
PHM|ommatidium
}

REFDSR
{
RDID|FBrf0105224
|Emerald and Roy
|1998
PHP|Homozygous clones can block the development of large portions of the
|external genitalia in males; in extreme cases the external genitalia
|consist of only portions of the anal plate and claspers and the penis
|apparatus is completely absent. The female genitalia are less affected
|by homozygous clones; the long bristles are absent and the thorn bristles
|are duplicated.
PHM|male genitalia | somatic clone
|penis | somatic clone
|gonopod thorn bristle | somatic clone
|gonopod long bristle | somatic clone
}

REFDSR
{
RDID|FBrf0108513
|Dominguez
|1999
PHP|When analyzed in large clones in the developing eye the packing in
|the ommatidial clusters is disrupted.
PHM|ommatidial cluster
}

REFDSR
{
RDID|FBrf0110710
|Sanson et al.
|1999
PHP|When <fbsym>FBal0050824==wg<up>Scer\UAS.cLa</up></fbsym> is driven by
| <fbsym>FBal0052377==Scer\GAL4<up>en-e16E</up></fbsym> in a <fbsym>FBal0031481==hh<up>AC</up></fbsym>
|embryo, denticle rows 2, 3 and 4 are replaced by naked cuticle. Rows
|5 and 6 are replaced by small denticles. In heterozygotes for <fbsym>FBal0031481==hh<up>AC</up></fbsym>,
|carrying <fbsym>FBal0050824==wg<up>Scer\UAS.cLa</up></fbsym> and
| <fbsym>FBal0052377==Scer\GAL4<up>en-e16E</up></fbsym>, occasional breaches
|in the normal denticle belts occur as patches of naked cuticle, revealing
|a dosage sensitivity to the requirement for <fbsym>FBgn0004644==hh</fbsym> function at the segment
|border.
PHM|embryonic epidermis
|denticle row 2
|denticle row 3
|denticle row 4
|denticle row 5
|denticle row 6
}

REFDSR
{
RDID|FBrf0122981
|Burke et al.
|1999
PHP|Homozygous embryos show a segment polarity phenotype.
|Large clones in the posterior compartment of the wing have a similar
|phenotype to <fbsym>FBal0102761==disp<up>S037707</up></fbsym> clones, except that wing
| vein L4 is additionally
|disrupted.
PHM|segment polarity
|wing | somatic clone
|wing vein L4 | somatic clone
}

REFDSR
{
RDID|FBrf0130058
|Rusch and Kaufman
|2000
PHP|The gnathal lobes are reduced in mutant embryos.
PHM|embryonic gnathal segment
}

REFDSR
{
RDID|FBrf0131292
|Gallet et al.
|2000
PHP|No segmentation is seen in <fbsym>FBal0031481==hh<up>AC</up></fbsym> mutant embryos.
| Naked cuticle
|is absent and no denticle diversity is seen (only type 5 denticles
|are present).
PHM|embryonic/first instar larval cuticle
|denticle belt | supernumerary
|denticle belt
}

REFDSR
{
RDID|FBrf0134579
|Methot and Basler
|2001
PHP|Mutant embryos are short and show a "lawn of denticles" phenotype.
PHM|embryonic/first instar larval cuticle
|denticle belt
}

REFDSR
{
RDID|FBrf0135716
|Lee et al.
|2001
PHP|<fbsym>FBal0031490==hh<up>ts2</up></fbsym>/<fbsym>FBal0031481==hh<up>AC</up></fbsym> embryos have a
| severe segment polarity phenotype,
|in which the naked cuticle is lost, at the restrictive temperature.
PHM|(with hh<up>ts2</up>) embryonic/first instar larval cuticle & segment polarity
}

REFDSR
{
RDID|FBrf0138357
|Vied and Horabin
|2001
PHP|98.9% of <fbsym>FBal0031490==hh<up>ts2</up></fbsym>/<fbsym>FBal0031481==hh<up>AC</up></fbsym>
| ovarioles contain multi-chambered cysts.
|Branching of the fusome occurs closer to the anterior end of the germarium
|than in wild type.
PHM|(with hh<up>ts2</up>) ovariole
}

REFDSR
{
RDID|FBrf0138370
|Deshpande et al.
|2001
PHP|Neuroblast NB 7-3 is missing in 40% of mutant hemisegments.
PHM|neuroblast NB7-3
}

REFDSR
{
RDID|FBrf0148964
|Lawrence et al.
|2002
PHM|adult cuticle & abdomen | somatic clone with <fbsym>FBal0032520==ptc<up>S2</up></fbsym>
}

REFDSR
{
RDID|FBrf0151279
|Besse et al.
|2002
PHP|Ovaries of <fbsym>FBal0031481==hh<up>AC</up></fbsym>/<fbsym>FBal0031490==hh<up>ts2</up></fbsym>
| females maintained at the restrictive
|temperature (29<up>o</up>C) for 4-5 days show a number of defects including
|multicyst egg chambers. Large groups of disorganized somatic cells
|are seen at the periphery of the germaria and multicyst egg chambers.
PHM|(with hh<up>ts2</up>) egg chamber
}

REFDSR
{
RDID|FBrf0155685
|Gallet et al.
|2003
PHP|The ventral cuticles of <fbsym>FBal0031481==hh<up>AC</up></fbsym> embryos are transformed
| into a lawn
|of row 5 type denticles (i.e.- no naked cuticle is formed).
PHM|denticle row 1
|denticle row 2
|denticle row 3
|denticle row 4
|denticle row 6
|denticle row 5 | ectopic
|embryonic/first instar larval cuticle | ventral
}

REFDSR
{
RDID|FBrf0167512
|Desbordes and Sanson
|2003
PHP|The areas of naked cuticle are replaced by denticles in the mutant
|embryos, resulting in a "lawn of denticles" without clear polarity.
PHM|embryonic/first instar larval cuticle | segment polarity
|denticle | ectopic
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
REFM|FBrf0064592
|Ma et al.
|1993
REFM|FBrf0091006
|Andrew et al.
|1997
REFM|FBrf0098358
|Strutt and Mlodzik
|1997
REFM|FBrf0099759
|Dominguez and Hafen
|1997
REFM|FBrf0105224
|Emerald and Roy
|1998
REFM|FBrf0108513
|Dominguez
|1999
REFM|FBrf0110710
|Sanson et al.
|1999
REFM|FBrf0122981
|Burke et al.
|1999
REFM|FBrf0130058
|Rusch and Kaufman
|2000
REFM|FBrf0131292
|Gallet et al.
|2000
REFM|FBrf0134579
|Methot and Basler
|2001
REFM|FBrf0135716
|Lee et al.
|2001
REFM|FBrf0138357
|Vied and Horabin
|2001
REFM|FBrf0138370
|Deshpande et al.
|2001
REFM|FBrf0148964
|Lawrence et al.
|2002
REFM|FBrf0151279
|Besse et al.
|2002
REFM|FBrf0155685
|Gallet et al.
|2003
REFM|FBrf0167512
|Desbordes and Sanson
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013022	ICL 1 P	SYM 1 P{?'}hh<up>AE</up>	ASTR 1 -	CLOC 1 94E1	REF 1 2	DT 1 14 Sep 1999	RESZ 507
ID|FBti0013022
SYM|P{?'}hh<up>AE</up>
SYN|P{?'}hh<up>AE</up>
ASTP|<fbsym>FBtp0002762==P{?'}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|P
ASGN|<fbsym>FBgn0004644==hh</fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
SYN|P{?'}hh<up>AE</up>
ASAL|<fbsym>FBal0031482==hh<up>AE</up></fbsym>
CLOC|94E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004644==hh</fbsym>
PHC|lethal | recessive
|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031482==hh<up>AE</up></fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
PHP|Extreme hh cuticle phenotype when heterozygous with
| <fbsym>FBal0005470==hh<up>9</up></fbsym>, or when
|homozygous. Head segments fail to involute, naked cuticle portion
|of segment lost causing half size embryos with a lawn of denticles.
|When heterozygous with <fbsym>FBal0005465==hh<up>4</up></fbsym> at 18<up>o</up>C, adults
| show mild eye phenotype,
|but there is no mutant eye phenotype when heterozygous with <fbsym>FBal0031487==hh<up>bar3</up></fbsym>.
|Homozygous embryos exhibit failure head involution and loss of naked
|cuticle from the posterior surface of each segment. Lethal when in
|... (see <fbsym>FBal0031482==hh<up>AE</up></fbsym> report)
PHM|embryonic head
|denticle belt
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013023	ICL 1 P	SYM 1 P{?'}hh<up>AM</up>	ASTR 1 -	CLOC 1 94E1	REF 1 2	DT 1 14 Sep 1999	RESZ 507
ID|FBti0013023
SYM|P{?'}hh<up>AM</up>
SYN|P{?'}hh<up>AM</up>
ASTP|<fbsym>FBtp0002762==P{?'}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|P
ASGN|<fbsym>FBgn0004644==hh</fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
SYN|P{?'}hh<up>AM</up>
ASAL|<fbsym>FBal0031483==hh<up>AM</up></fbsym>
CLOC|94E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004644==hh</fbsym>
PHC|lethal | recessive
|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031483==hh<up>AM</up></fbsym>

REFDSR
{
RDID|FBrf0055558
|Lee et al.
|1992
PHP|Mild hh cuticle phenotype when heterozygous with
| <fbsym>FBal0005470==hh<up>9</up></fbsym>, or when homozygous,
|with occasional abdominal and thoracic denticle belt fusions. When
|heterozygous with <fbsym>FBal0005465==hh<up>4</up></fbsym>, at 18<up>o</up>C, some adults
| are produced, with wild
|type eyes. Eyes wild type over <fbsym>FBal0031487==hh<up>bar3</up></fbsym>.
|Homozygous embryos exhibit occasional abdominal and thoracic denticle
|belt fusions. Lethal when in homozygous or heterozygous combination
|with <fbsym>FBal0005466==hh<up>5</up></fbsym>, <fbsym>FBal0005469==hh<up>8</up></fbsym> or
| <fbsym>FBal0005470==hh<up>9</up></fbsym>. Transheterozygotes with <fbsym>FBal0005465==hh<up>4</up></fbsym>
|... (see <fbsym>FBal0031483==hh<up>AM</up></fbsym> report)
PHM|denticle belt
}

REF
{
REFM|FBrf0055558
|Lee et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013266	ICL 1 P	SYM 1 P{lacW}elav<up>E</up>	ASTR 1 +	CLOC 1 1B7--8	REF 1 2	DT 1 14 Sep 1999	RESZ 1201
ID|FBti0013266
SYM|P{lacW}elav<up>E</up>
SYN|E
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|P
ASGN|<fbsym>FBgn0000570==elav</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>
ASTR|<fbsym>FBtr0005150==Ecol\lacZ<up>elav-E</up>RA</fbsym>

REFDSR
{
RDID|FBrf0053818
|Prokop and Technau
|1991
CVBODPC|In third instar larva, appears to be expressed in all cells of the CNS.
| (Note:expression of <fbsym>FBti0013266==P{lacW}elav<up>E</up></fbsym> and <fbsym>FBti0013273==P{lacW}B1</fbsym>
| assayed together, in strain homozygous for both insertions.)
CVBODP|transcript distribution deduced from reporter protein
|<t> L | third instar larva stage 2 <a> larval central nervous system <p>
PHC|viable
|fertile
}

REFDSR
{
RDID|FBrf0103505
|Prokop et al.
|1998
SYN|E
ASAL|<fbsym>FBal0098864==Ecol\lacZ<up>elav-E</up></fbsym>
|<fbsym>FBal0098742==elav<up>E</up></fbsym>
CLOC|1B7--8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000570==elav</fbsym>
CVBODP|transcript distribution deduced from reporter protein
|<t> E <a> embryonic nervous system <p>
CC|Obtained from collection of E. Bier.
}

REF
{
REFM|FBrf0053818
|Prokop and Technau
|1991
REFM|FBrf0103505
|Prokop et al.
|1998
}

}

# EOR

TIR
{

RETE|ID 1 FBti0013361	ICL 1 P	SYM 1 P{bluetail}Abd-B<up>blt</up>	ASTR 1 -	CLOC 1 89E4--5	REF 1 7	DT 1 5 Nov 1999	RESZ 833
ID|FBti0013361
SYM|P{bluetail}Abd-B<up>blt</up>
SYN|bluetail
ASTP|<fbsym>FBtp0006523==P{bluetail}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0000015==Abd-B</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0058131
|Galloni et al.
|1993
SYN|P{bluetail}Abd-B<up>blt</up>
ASAL|<fbsym>FBal0028670==Abd-B<up>blt</up></fbsym>
|<fbsym>FBal0176213==Ecol\lacZ<up>Abd-B-blt</up></fbsym>
CLOC|89E4--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000015==Abd-B</fbsym>
}

REFDSR
{
RDID|FBrf0141654
|Hogga et al.
|2001
SYN|bluetail
}

REF
{
REFM|FBrf0058131
|Galloni et al.
|1993
REFM|FBrf0074694
|Vazquez et al.
|1993
REFM|FBrf0082148
|Hogga and Karch
|1995
REFM|FBrf0091065
|Hagstrom et al.
|1996
REFM|FBrf0093606
|Mihaly et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0141654
|Hogga et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0028670==Abd-B<up>blt</up></fbsym>

REFDSR
{
RDID|FBrf0058131
|Galloni et al.
|1993
PHP|Males exhibit a rudimentary 7th tergite.
PHM|abdominal tergite 7 | male
}

REFDSR
{
RDID|FBrf0074694
|Vazquez et al.
|1993
PHP|Weak iab7 phenotype.
}

REFDSR
{
RDID|FBrf0080088
|Hendrickson and Sakonju
|1995
PHP|Segments A6 and A7 show a more posterior identity when heterozygous
|with <fbsym>FBgn0000015==Abd-B</fbsym><up>-</up> than when hemizygous.
PHM|adult abdominal segment 6
|adult abdominal segment 7
}

REF
{
REFM|FBrf0058131
|Galloni et al.
|1993
REFM|FBrf0074694
|Vazquez et al.
|1993
REFM|FBrf0080088
|Hendrickson and Sakonju
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013377	ICL 1 P	SYM 1 P{scrt.sE}lz<up>Sprite</up>	ASTR 1 -	CLOC 1 8D5--6	REF 1 2	DT 1 5 Nov 1999	RESZ 452
ID|FBti0013377
SYM|P{scrt.sE}lz<up>Sprite</up>
ASTP|<fbsym>FBtp0005706==P{scrt.sE}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0002576==lz</fbsym>

REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
SYN|P{scrt.sE}lz<up>Sprite</up>
ASAL|<fbsym>FBal0050114==lz<up>Sprite</up></fbsym>
CLOC|8D5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002576==lz</fbsym>
}

REF
{
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0050114==lz<up>Sprite</up></fbsym>

REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|Conversion of outer photoreceptor neurons R3 and R4 to ventral R7-like
|photoreceptor, a dosage sensitive phenotype (R4 is more sensitive to
|conversion than R3). The fate of these R7-like cells is partially
|dependent on <fbsym>FBgn0003366==sev</fbsym> function, in a <fbsym>FBal0015458==sev<up>14</up></fbsym> background
| many R7-like
|cells fail to develop as photoreceptor neurons.
| <fbsym>FBal0015458==sev<up>14</up></fbsym>, <fbsym>FBal0050114==lz<up>Sprite</up></fbsym>
|double mutants display wild-type phototactic behavior (migrate towards
|the UV light source) demonstrating the converted R7-like cells function
|... (see <fbsym>FBal0050114==lz<up>Sprite</up></fbsym> report)
PHM|photoreceptor cell R3
|photoreceptor cell R4
}

REFDSR
{
RDID|FBrf0104748
|Flores et al.
|1998
PHP|The presumptive R3/R4 photoreceptor cells differentiate as R7 cells
|in flies carrying <fbsym>FBal0050114==lz<up>Sprite</up></fbsym>.
PHM|photoreceptor cell R3
|photoreceptor cell R4
}

REFDSR
{
RDID|FBrf0132427
|Clandinin and Zipursky
|2000
PHP|R3 and R4 are transformed to R7 cells. In completely transformed ommatidia
|the relative positions of the targets chosen by R1, R2, R5 and R6 are
|frequently highly aberrant. Ommatidia are normally rotated.
PHM|photoreceptor cell R3
|photoreceptor cell R4
|photoreceptor cell R1 & axon
|photoreceptor cell R2 & axon
|photoreceptor cell R5 & axon
|photoreceptor cell R6 & axon
}

REF
{
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0104748
|Flores et al.
|1998
REFM|FBrf0132427
|Clandinin and Zipursky
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013380	ICL 1 P	SYM 1 P{UAS-drl}i	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Nov 1999	RESZ 341
ID|FBti0013380
SYM|P{UAS-drl}i
ASTP|<fbsym>FBtp0007327==P{UAS-drl}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0015380==drl</fbsym>

REFDSR
{
RDID|FBrf0090483
|Callahan et al.
|1996
SYN|P{UAS-drl}i
ASAL|<fbsym>FBal0057582==drl<up>i</up></fbsym>
}

REF
{
REFM|FBrf0090483
|Callahan et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0057582==drl<up>i</up></fbsym>

REFDSR
{
RDID|FBrf0090483
|Callahan et al.
|1996
PHP|Two copies of <fbsym>FBti0013380==P{UAS-drl}i</fbsym> show nearly complete rescue of the <fbsym>FBal0045521==drl<up>R343</up></fbsym>
|embryonic 'bypass' phenotype.
}

REF
{
REFM|FBrf0090483
|Callahan et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013404	ICL 1 P	SYM 1 P{UAS-Ubx.IVa.W}K's	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 19 Feb 2001	RESZ 382
ID|FBti0013404
SYM|P{UAS-Ubx.IVa.W}K's
SYN|P{UAS.Ubx-IVa.W}K's
ASTP|<fbsym>FBtp0009567==P{UAS-Ubx.IVa.W}</fbsym>
DT|19 Feb 2001
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
SYN|P{UAS.Ubx-IVa.W}K's
ASAL|<fbsym>FBal0090058==w<up>K's</up></fbsym>
}

REF
{
REFM|FBrf0102846
|Netter et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0090058==w<up>K's</up></fbsym>

REFDSR
{
RDID|FBrf0102846
|Netter et al.
|1998
PHP|Pigmented area corresponds to dorsal half of the eye, with a pigmentation
|level ranging from orange to red. Ventral section of eye is white.
PHM|pigment cell
}

REF
{
REFM|FBrf0102846
|Netter et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013411	ICL 1 P	SYM 1 P{DMR}tsh<up>Fe</up>	ASTR 1 -	CLOC 1 40A5	REF 1 2	DT 1 5 Nov 1999	RESZ 435
ID|FBti0013411
SYM|P{DMR}tsh<up>Fe</up>
ASTP|<fbsym>FBtp0010462==P{DMR}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0003866==tsh</fbsym>

REFDSR
{
RDID|FBrf0105904
|Pan and Rubin
|1998
SYN|P{DMR}tsh<up>Fe</up>
ASAL|<fbsym>FBal0095156==tsh<up>Fe</up></fbsym>
CLOC|40A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003866==tsh</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105904
|Pan and Rubin
|1998
}

ALESR
{
ASYM|<fbsym>FBal0095156==tsh<up>Fe</up></fbsym>

REFDSR
{
RDID|FBrf0105904
|Pan and Rubin
|1998
PHP|Ectopic eye formation in the anterior region of the head, just ventral
|to the antenna. The ectopic eyes have nearly normal facets with interommatidial
|bristles, cone cells, pigment cells, photoreceptors and rhabdomeres.
|Ectopic eyes also appear on the antenna but are smaller and occur
|with lower frequency.
|Ectopic eyes are not seen on any other adult structure.
|An arista to leg transformation also occurs. A claw appears on the
|... (see <fbsym>FBal0095156==tsh<up>Fe</up></fbsym> report)
PHM|adult head
|arista
|head & eye | ectopic
|antenna & eye | ectopic
|eye | ectopic
|leg | ectopic
}

REF
{
REFM|FBrf0105904
|Pan and Rubin
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013480	ICL 1 P	SYM 1 P{UAS-hep.CA}CA	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Nov 1999	RESZ 363
ID|FBti0013480
SYM|P{UAS-hep.CA}CA
ASTP|<fbsym>FBtp0011052==P{UAS-hep.CA}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0010303==hep</fbsym>

REFDSR
{
RDID|FBrf0108559
|Adachi-Yamada et al.
|1999
SYN|P{UAS-hep.CA}CA
ASAL|<fbsym>FBal0098235==hep<up>CA</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108559
|Adachi-Yamada et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0098235==hep<up>CA</up></fbsym>

REFDSR
{
RDID|FBrf0108559
|Adachi-Yamada et al.
|1999
PHP|<fbsym>FBal0098235==hep<up>CA</up></fbsym> heterozygotes show notching of the wing in
| less than 10%
|of cases.
|Massive cell death is seen in both the proximal and distal wing primordia
|in the <fbsym>FBal0098235==hep<up>CA</up></fbsym> late third larval instar wing disc.
PHM|wing
|dorsal mesothoracic disc
}

REFDSR
{
RDID|FBrf0145123
|Chen et al.
|2002
PHP|10% of heterozygous flies lack part of the wing.
PHM|wing
}

REF
{
REFM|FBrf0108559
|Adachi-Yamada et al.
|1999
REFM|FBrf0145123
|Chen et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013484	ICL 1 P	SYM 1 P{hs-&lgr;top}Mod	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Nov 1999	RESZ 409
ID|FBti0013484
SYM|P{hs-&lgr;top}Mod
SYN|lambda-top<up>HS-mod</up>
ASTP|<fbsym>FBtp0011214==P{hs-&lgr;top}</fbsym>
DT|5 Nov 1999
|5 Nov 1999
ICL|P
ASGN|<fbsym>FBgn0022739==btl::Egfr</fbsym>

REFDSR
{
RDID|FBrf0108778
|Guichard et al.
|1999
SYN|lambda-top<up>HS-mod</up>
ASAL|<fbsym>FBal0098773==btl::Egfr<up>Mod</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108778
|Guichard et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0098773==btl::Egfr<up>Mod</up></fbsym>

REFDSR
{
RDID|FBrf0108778
|Guichard et al.
|1999
PHP|Homozygous insertions cause a moderate extra-vein phenotype.
PHM|wing
}

REF
{
REFM|FBrf0108778
|Guichard et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014085	ICL 1 Doc	SYM 1 Doc{}Antp<up>Doc</up>	ASTR 1 -	CLOC 1 84A6--B2	REF 1 2	DT 1 6 Jan 2000	RESZ 448
ID|FBti0014085
SYM|Doc{}Antp<up>Doc</up>
ASTP|<fbsym>FBtp0011424==Doc</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Doc
ASGN|<fbsym>FBgn0000095==Antp</fbsym>

REFDSR
{
RDID|FBrf0073744
|Lim and Simmons
|1994
SYN|Doc{}Antp<up>Doc</up>
ASAL|<fbsym>FBal0028935==Antp<up>Doc</up></fbsym>
CLOC|84A6--B2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000095==Antp</fbsym>
}

REF
{
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014101	ICL 1 ?	SYM 1 ?{}Bx<up>M</up>	ASTR 1 -	CLOC 1 17C3--4	REF 1 2	DT 1 6 Jan 2000	RESZ 407
ID|FBti0014101
SYM|?{}Bx<up>M</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0000242==Bx</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}Bx<up>M</up>
ASAL|<fbsym>FBal0001443==Bx<up>M</up></fbsym>
MU|spontaneous
CLOC|17C3--4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000242==Bx</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014102	ICL 1 P	SYM 1 P{Bm&Dgr;-w}CycA<up>hari</up>	ASTR 1 -	CLOC 1 68E1	REF 1 4	DT 1 21 Nov 2000	RESZ 582
ID|FBti0014102
SYM|P{Bm&Dgr;-w}CycA<up>hari</up>
SYN|P{}CycA<up>hari</up>
ASTP|<fbsym>FBtp0000774==P{Bm&Dgr;-w}</fbsym>
DT|21 Nov 2000
|6 Jan 2000
ICL|P
PRG|P{Bm&Dgr;-w}mw474
ASGN|<fbsym>FBgn0000404==CycA</fbsym>

REFDSR
{
RDID|FBrf0055951
|Ueda et al.
|1992
SYN|P{}CycA<up>hari</up>
ASAL|<fbsym>FBal0002204==CycA<up>hari</up></fbsym>
CLOC|68E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000404==CycA</fbsym>
}

REF
{
REFM|FBrf0055951
|Ueda et al.
|1992
REFM|FBrf0056094
|Takahisa et al.
|1992
REFM|FBrf0091062
|Gordadze and Benes
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002204==CycA<up>hari</up></fbsym>

REFDSR
{
RDID|FBrf0051379
|Lehner and O'Farrell
|1990
PHP|Abrupt disappearance of CycB that normally accompanies mitosis do not
|occur. The changes in the pattern of CycB expression result from controls
|at the transcript level.
}

REFDSR
{
RDID|FBrf0055951
|Ueda et al.
|1992
PHP|Homozygous flies exhibit bristle defects. Sensory mother cells do
|not divide properly: loss or abnormalities of adult mechanosensory
|organs.
}

REFDSR
{
RDID|FBrf0056094
|Takahisa et al.
|1992
PHP|Abnormal bristles in adult. Homozygotes miss bristles and/or sockets
|(see Ueda et al., EMBO J. 11: 2935-2939).
}

REF
{
REFM|FBrf0051379
|Lehner and O'Farrell
|1990
REFM|FBrf0055951
|Ueda et al.
|1992
REFM|FBrf0056094
|Takahisa et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014111	ICL 1 P	SYM 1 P{}Dl<up>P-N</up>	ASTR 1 -	CLOC 1 92A1--2	REF 1 2	DT 1 6 Jan 2000	RESZ 463
ID|FBti0014111
SYM|P{}Dl<up>P-N</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000463==Dl</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}Dl<up>P-N</up>
ASAL|<fbsym>FBal0002629==Dl<up>P-N</up></fbsym>
MU|P-element activity
CLOC|92A1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000463==Dl</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014112	ICL 1 P	SYM 1 P{}Doa<up>HD</up>	ASTR 1 -	CLOC 1 98F1--2	REF 1 5	DT 1 19 Feb 2001	RESZ 909
ID|FBti0014112
SYM|P{}Doa<up>HD</up>
SYN|P{}Doa<up>1</up>
|P{}Doa<up>2</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|19 Feb 2001
|6 Jan 2000
ICL|P
ID2|FBti0014113
ASGN|<fbsym>FBgn0053553==Doa</fbsym>

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0058584
|Rabinow et al.
|1993
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0074875
|Yun et al.
|1994
SYN|P{}Doa<up>1</up>
|P{}Doa<up>2</up>
ASAL|<fbsym>FBal0002719==Doa<up>HD</up></fbsym>
MU|PM hybrid dysgenesis
CLOC|98F1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0053553==Doa</fbsym>
}

REFDSR
{
RDID|FBrf0130184
|Yun et al.
|2000
PHC|(with Df(3R)3450) lethal
|(with Doa<up>01705b</up>) lethal
}

REF
{
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0058584
|Rabinow et al.
|1993
REFM|FBrf0074875
|Yun et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130184
|Yun et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0002719==Doa<up>HD</up></fbsym>

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
PHP|Crosses between <fbsym>FBal0002719==Doa<up>HD</up></fbsym> and
| <fbsym>FBal0002727==Doa<up>9</up></fbsym> heterozygotes indicate that <fbsym>FBgn0000480==Doa</fbsym>
|is not an embryonic lethal, and is probably lethal during early larval
|stages.
|Rare <fbsym>FBal0002719==Doa<up>HD</up></fbsym>/<fbsym>FBal0002724==Doa<up>6</up></fbsym> or
| <fbsym>FBal0002719==Doa<up>HD</up></fbsym>/<fbsym>FBal0002725==Doa<up>7</up></fbsym> escapers of
| lethality are
|found at a frequency of approximately 0.5%. <fbsym>FBal0002719==Doa<up>HD</up></fbsym>/<fbsym>FBal0002724==Doa<up>6</up></fbsym>
|escapers are more frequently female than male (ratio 4:1) and the male
|escapers are sterile despite having motile sperm.
}

REFDSR
{
RDID|FBrf0074875
|Yun et al.
|1994
PHP|Heterozygotes with <fbsym>FBal0002725==Doa<up>7</up></fbsym> have ommatidia of varying
| size and disorganization
|of the interommatidial bristles. Random interruption of the normal
|lattice of pigment cells and random vacuolization of the retina and
|pigment cells are restored to at least normal levels (suppression of
|<fbsym>FBal0018195==w<up>a</up></fbsym>).
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Heterozygotes with <fbsym>FBal0002724==Doa<up>6</up></fbsym> or
| <fbsym>FBal0002725==Doa<up>7</up></fbsym> survive rarely and when they do,
| <fbsym>FBal0018195==w<up>a</up></fbsym> is
|darkened to nearly wild-type color; <fbsym>FBal0018306==w<up>sp55</up></fbsym> reacts in
|the opposite manner, becoming nearly white; eyes of
|escapers have disarranged facets. Males of these
|heteroallelic combinations involving <fbsym>FBal0002724==Doa<up>6</up></fbsym> are
|sterile despite having motile sperm; females and both
|sexes involving <fbsym>FBal0002725==Doa<up>7</up></fbsym> are weakly fertile.
}

REF
{
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0074875
|Yun et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014115	ICL 1 hopper	SYM 1 hopper{}Dsim\N<up>fa-Ds</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 6 Jan 2000	RESZ 464
ID|FBti0014115
SYM|hopper{}Dsim\N<up>fa-Ds</up>
ASTP|<fbsym>FBtp0011438==hopper</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|hopper
ASGN|<fbsym>FBgn0012846==Dsim\N</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|hopper{}Dsim\N<up>fa-Ds</up>
ASAL|<fbsym>FBal0029503==Dsim\N<up>fa-Ds</up></fbsym>
MU|spontaneous
LOCB|Proximity to gene: <fbsym>FBgn0012846==Dsim\N</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014166	ICL 1 P	SYM 1 P{}N<up>DTV</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 3	DT 1 6 Jan 2000	RESZ 570
ID|FBti0014166
SYM|P{}N<up>DTV</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0004647==N</fbsym>

REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}N<up>DTV</up>
ASAL|<fbsym>FBal0012764==N<up>DTV</up></fbsym>
MU|PM hybrid dysgenesis
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012764==N<up>DTV</up></fbsym>

REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
PHP|Heterozygous females show wing nicking.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Shows standard N phenotype in homo- and heterozygotes;
}

REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014167	ICL 1 FB	SYM 1 FB{}N<up>M</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 3	DT 1 6 Jan 2000	RESZ 555
ID|FBti0014167
SYM|FB{}N<up>M</up>
ASTP|<fbsym>FBtp0011426==FB</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|FB
ASGN|<fbsym>FBgn0004647==N</fbsym>

REFDSR
{
RDID|FBrf0063371
|Cicak and Oster
|1957
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|FB{}N<up>M</up>
ASAL|<fbsym>FBal0012780==N<up>M</up></fbsym>
MU|spontaneous
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0063371
|Cicak and Oster
|1957
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012780==N<up>M</up></fbsym>

REFDSR
{
RDID|FBrf0063371
|Cicak and Oster
|1957
PHP|Lethal in hemizygous males. Females show notching of the tips and
|occasionally of the edges of the wing, have thickened veins which broaden
|to form deltas, slightly smaller eyes than normal and infrequently
|a gross reduction of one eye.
| <fbsym>FBal0012780==N<up>M</up></fbsym>/<fbsym>FBal0012900==N<up>spl-1</up></fbsym> flies have roughened
|eyes which are smaller than normal and split bristles.
PHM|wing
|wing vein
|eye
|macrochaeta
}

REF
{
REFM|FBrf0063371
|Cicak and Oster
|1957
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014168	ICL 1 P	SYM 1 P{}N<up>PI</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 3	DT 1 6 Jan 2000	RESZ 567
ID|FBti0014168
SYM|P{}N<up>PI</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0004647==N</fbsym>

REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}N<up>PI</up>
ASAL|<fbsym>FBal0012784==N<up>PI</up></fbsym>
MU|PM hybrid dysgenesis
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012784==N<up>PI</up></fbsym>

REFDSR
{
RDID|FBrf0046957
|Kelley et al.
|1987
PHP|Heterozygous females show wing nicking.
}

REF
{
REFM|FBrf0046957
|Kelley et al.
|1987
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014169	ICL 1 ?	SYM 1 ?{}N<up>S</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 4	DT 1 6 Jan 2000	RESZ 613
ID|FBti0014169
SYM|?{}N<up>S</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0004647==N</fbsym>

REFDSR
{
RDID|FBrf0039985
|Kramers et al.
|1983
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}N<up>S</up>
ASAL|<fbsym>FBal0012785==N<up>S</up></fbsym>
MU|spontaneous
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0039985
|Kramers et al.
|1983
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012785==N<up>S</up></fbsym>

REFDSR
{
RDID|FBrf0045066
|Schalet
|1986
PHP|Heterozygotes display a weak notched wing phenotype.
PHM|wing
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Weak Notch. <fbsym>FBal0012785==N<up>S</up></fbsym>/<fbsym>FBal0012860==N<up>Ax-S</up></fbsym> is lethal.
}

REF
{
REFM|FBrf0045066
|Schalet
|1986
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014172	ICL 1 flea	SYM 1 flea{}N<up>fa-fx</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 2	DT 1 6 Jan 2000	RESZ 522
ID|FBti0014172
SYM|flea{}N<up>fa-fx</up>
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|flea
ASGN|<fbsym>FBgn0004647==N</fbsym>
SK|FBst0000048
|N[fa-fx]/C(1)DX, y[1] f[1]
|Total=1

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|flea{}N<up>fa-fx</up>
ASAL|<fbsym>FBal0012867==N<up>fa-fx</up></fbsym>
MU|<up>3</up>H-thymidine
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012867==N<up>fa-fx</up></fbsym>

REFDSR
{
RDID|FBrf0054541
|Markopoulou and Artavanis-Tsakonas
|1991
PHP|Retina defects are associated with optic lobe defects in 100% of homozygous
|<fbsym>FBal0012867==N<up>fa-fx</up></fbsym> retina clones generated by somatic
| recombination. The arrangement
|of ommatidia is severely disrupted, the number of ommatidia is reduced
|and they appear shorter than normal in homozygous clones in the retina.
|A disruption of the fenestrated zone, laminar cortex and neuropil
|can be seen in the underlying optic lobe. Homozygous late pupae have
|normal optic lobe morphology, but the lamina neuropil is severely disrupted,
|... (see <fbsym>FBal0012867==N<up>fa-fx</up></fbsym> report)
PHM|lamina neuropil
|medulla neuropil
|retina | somatic clone | cell autonomous
|optic lobe | somatic clone | cell autonomous
|ommatidium | somatic clone | cell autonomous
|optic neuropil | somatic clone | cell autonomous
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Strong echinus-like eyes, darkening with age with
|glistening frosted appearance. Homozygous females
|sterile, but sterility may be separable from <fbsym>FBal0012867==N<up>fa-fx</up></fbsym>
|(Kaplan and Hayes, 1967).
|strong allele; not dosage compensated
}

REF
{
REFM|FBrf0054541
|Markopoulou and Artavanis-Tsakonas
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014173	ICL 1 flea	SYM 1 flea{}N<up>fa-g</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 3	DT 1 6 Jan 2000	RESZ 926
ID|FBti0014173
SYM|flea{}N<up>fa-g</up>
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|flea
ASGN|<fbsym>FBgn0004647==N</fbsym>
SK|FBst0002886
|w[a] N[fa-g]; l(2)52Fe[E6.17]/CyO
|FBst0003072
|w[a] N[fa-g]; l(2)52Fd[E3.27]/CyO
|FBst0003176
|w[a] N[fa-g]; Rho1[E3.10]/CyO
|FBst0003339
|w[a] N[fa-g]; l(2)52Fc[D8.13]/CyO
|FBst0003517
|w[a] N[fa-g]; Df(2R)Jp4/CyO
|FBst0003518
|w[a] N[fa-g]; Df(2R)Jp1/CyO
|FBst0003520
|w[a] N[fa-g]; Df(2R)Jp8, w[+]/CyO
|FBst0003521
|w[a] N[fa-g]; Df(2R)Jp6/CyO
|FBst0003522
|w[a] N[fa-g]; Df(2R)Jp7, w[+]/CyO
|Total=9

REFDSR
{
RDID|FBrf0051947
|Rabinow and Birchler
|1990
SYN|flea{}N<up>fa-g</up>
ASAL|<fbsym>FBal0012868==N<up>fa-g</up></fbsym>
MU|spontaneous
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0051947
|Rabinow and Birchler
|1990
REFM|FBrf0056273
|Gorman and Girton
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012868==N<up>fa-g</up></fbsym>

REFDSR
{
RDID|FBrf0027480
|Shellenbarger and Mohler
|1975
PHP|Homozygotes have rough eyes with a glossy surface. This phenotype
|is the same at 18, 25 and 29<up>o</up>C.
PHM|eye
|ommatidium
}

REFDSR
{
RDID|FBrf0044443
|Welshons and Welshons
|1986
PHP|Homozygous female and hemizygous male flies have rough, glossy eyes.
|<fbsym>FBal0012874==N<up>fa-swb</up></fbsym>/<fbsym>FBal0012868==N<up>fa-g</up></fbsym> flies have
| rough eyes that are not glossy.
PHM|eye
}

REFDSR
{
RDID|FBrf0049795
|Cagan and Ready
|1989
PHP|The eye has a smooth, glossy appearance, because the corneal lenses
|are separated by a shallow trough rather than a sharp crevice as in
|the wild-type. The ommatidial array is less regular than in normal
|eyes. Few ommachrome containing primary pigment cells are present,
|and there are excess pteridine-containing secondary-like pigment cells.
|Eye bristles are not properly placed. Cell death in the eye is reduced.
PHM|eye
|lens
|ommatidial cluster
|primary pigment cell
|secondary pigment cell
}

REFDSR
{
RDID|FBrf0049851
|Siren and Portin
|1989
PHP|Expression was suppressed by Dl mutations and enhanced by E(spl) and
|H mutations.
}

REFDSR
{
RDID|FBrf0051947
|Rabinow and Birchler
|1990
PHP|Homozygotes exhibit rough eyes due to misrouting of primary pigment
|cells to the fate of secondary pigment cells (FBrf0049795). Phenotype
|can be altered by <fbsym>FBgn0003326==sca</fbsym> mutations, necrotic patches of tissue appears
|in both eyes.
PHM|eye
}

REFDSR
{
RDID|FBrf0051969
|Xu and Artavanis-Tsakonas
|1990
PHP|Pronounced eye phenotype. Does not interact with <fbsym>FBal0031145==dx<up>ENU</up></fbsym>.
}

REFDSR
{
RDID|FBrf0054255
|Portin and Rantanen
|1991
PHP|Mutations of mam, bib and neur in an heterozygous condition had no
|effect on the expression of <fbsym>FBal0012854==N<up>Ax-59d</up></fbsym> or
| <fbsym>FBal0012853==N<up>Ax-59b</up></fbsym> except when
|coupled in cis with <fbsym>FBal0012868==N<up>fa-g</up></fbsym>. The neurogenic mutations
| suppress the
|wing venation phenotype of N.
}

REFDSR
{
RDID|FBrf0054541
|Markopoulou and Artavanis-Tsakonas
|1991
PHP|Retina defects are not associated with optic lobe defects in 50% of
|homozygous <fbsym>FBal0012868==N<up>fa-g</up></fbsym> retina clones generated by somatic recombination.
|The arrangement of ommatidia is severely disrupted, the number of
|ommatidia is reduced and they appear shorter than normal in homozygous
|clones in the retina. A disruption of the fenestrated zone, laminar
|cortex and neuropil can be seen in the underlying optic lobe if it
|is defective.
}

REFDSR
{
RDID|FBrf0055810
|Duus et al.
|1992
PHP|Rough eyes, irregular arrangements of facets and irregularities in
|internal retinal structures.
}

REFDSR
{
RDID|FBrf0056273
|Gorman and Girton
|1992
PHP|Glossy looking eyes. Additive interactions with dx alleles.
}

REFDSR
{
RDID|FBrf0063631
|Lefevre
|1974
PHP|<fbsym>FBal0012873==N<up>fa-l2</up></fbsym>/<fbsym>FBal0012868==N<up>fa-g</up></fbsym> flies have
| rough, irregular eyes.
PHM|eye
|ommatidium
}

REFDSR
{
RDID|FBrf0104448
|Hayashi et al.
|1998
PHP|Primary pigment cells are not formed in hemizygous flies.
PHM|primary pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eyes have facets more irregular than fa, but surface
|is smoothed, giving a glossy effect. Equal mutant
|expression in both sexes. Pigment distribution may be
|uneven, contributing to an impression of altered eye
|color. No wing effect. Eyes of <fbsym>FBal0012868==N<up>fa-g</up></fbsym>/<fbsym>FBal0012863==N<up>fa-1</up></fbsym>
|intermediate between the two homozygotes.
|Complementary with spl, <fbsym>FBal0012892==N<up>nd-3</up></fbsym>, nd and <fbsym>FBal0012891==N<up>nd-2</up></fbsym>
|... (see <fbsym>FBal0012868==N<up>fa-g</up></fbsym> report)
}

REF
{
REFM|FBrf0027480
|Shellenbarger and Mohler
|1975
REFM|FBrf0044443
|Welshons and Welshons
|1986
REFM|FBrf0049795
|Cagan and Ready
|1989
REFM|FBrf0049851
|Siren and Portin
|1989
REFM|FBrf0051947
|Rabinow and Birchler
|1990
REFM|FBrf0051969
|Xu and Artavanis-Tsakonas
|1990
REFM|FBrf0054255
|Portin and Rantanen
|1991
REFM|FBrf0054541
|Markopoulou and Artavanis-Tsakonas
|1991
REFM|FBrf0055810
|Duus et al.
|1992
REFM|FBrf0056273
|Gorman and Girton
|1992
REFM|FBrf0063631
|Lefevre
|1974
REFM|FBrf0104448
|Hayashi et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014177	ICL 1 flea	SYM 1 flea{}N<up>fa-swbBG</up>	ASTR 1 -	CLOC 1 3C7--9	REF 1 2	DT 1 6 Jan 2000	RESZ 454
ID|FBti0014177
SYM|flea{}N<up>fa-swbBG</up>
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|flea
ASGN|<fbsym>FBgn0004647==N</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|flea{}N<up>fa-swbBG</up>
ASAL|<fbsym>FBal0012875==N<up>fa-swbBG</up></fbsym>
CLOC|3C7--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004647==N</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0012875==N<up>fa-swbBG</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Flies have nicked wings.
PHM|wing
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014207	ICL 1 P	SYM 1 P{}Ser<up>Rpw</up>	ASTR 1 -	CLOC 1 97E6--8	REF 1 2	DT 1 6 Jan 2000	RESZ 442
ID|FBti0014207
SYM|P{}Ser<up>Rpw</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0004197==Ser</fbsym>

REFDSR
{
RDID|FBrf0079431
|Soanes and Bell
|1995
SYN|P{}Ser<up>Rpw</up>
ASAL|<fbsym>FBal0034012==Ser<up>Rpw</up></fbsym>
CLOC|97E6--8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004197==Ser</fbsym>
}

REF
{
REFM|FBrf0079431
|Soanes and Bell
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0034012==Ser<up>Rpw</up></fbsym>

REFDSR
{
RDID|FBrf0079431
|Soanes and Bell
|1995
PHP|Wing margin is incised. At 22<up>o</up>C heterozygotes show nicking around
|the entire margin, at 17<up>o</up>C the nicking is more extreme, at 29<up>o</up>C
|the phenotype overlaps wild type.
PHM|wing | conditional cs
}

REF
{
REFM|FBrf0079431
|Soanes and Bell
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014232	ICL 1 gypsy	SYM 1 gypsy{}Sxl<up>fLS</up>	ASTR 1 -	CLOC 1 6F3--5	REF 1 6	DT 1 6 Jan 2000	RESZ 816
ID|FBti0014232
SYM|gypsy{}Sxl<up>fLS</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0042036
|Maine et al.
|1985
SYN|gypsy{}Sxl<up>fLS</up>
ASAL|<fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>
CLOC|6F3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003659==Sxl</fbsym>
}

REFDSR
{
RDID|FBrf0053358
|Bell et al.
|1991
PHC|lethal | female
}

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHC|lethal | female | recessive
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHC|lethal
}

REF
{
REFM|FBrf0042036
|Maine et al.
|1985
REFM|FBrf0046351
|Salz et al.
|1987
REFM|FBrf0053358
|Bell et al.
|1991
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHP|Fully complemented by <fbsym>FBal0049190==Sxl<up>fb</up></fbsym>,
| <fbsym>FBal0030317==Sxl<up>fc</up></fbsym> and <fbsym>FBal0016686==Sxl<up>f9</up></fbsym>. Homozygous
|germ cell clones do not develop into oocytes.
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Able to initiate female development, but is defective in its ability
|to maintain the female developmental commitment and/or to elicit female
|sexual differentiation. It is masculinizing in homozygous mutant
|somatic clones induced by mitotic recombination and it causes the
|tissue in such clones to grow poorly; nevertheless, it has no dominant
|effect on the sexual phenotype of triploid intersexes, nor does it
|interact in a dominant fashion with mutations in <fbsym>FBgn0000413==da</fbsym> or <fbsym>FBgn0003411==sisA</fbsym>, both
|... (see <fbsym>FBal0016689==Sxl<up>fLS</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0072617
|Bernstein and Cline
|1994
PHP|<fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>/<fbsym>FBal0016680==Sxl<up>f1</up></fbsym> shows wild type
| dosage compensation in <fbsym>FBal0014870==run<up>25</up></fbsym>
|phenotype assay.
}

REFDSR
{
RDID|FBrf0076149
|Pultz and Baker
|1995
PHP|Survival of <fbsym>FBal0005441==her<up>1</up></fbsym>/<fbsym>FBal0009283==her<up>mat-1</up></fbsym>
| and <fbsym>FBal0005441==her<up>1</up></fbsym>/<fbsym>FBal0005442==her<up>2</up></fbsym> daughters not
|affected in the presence of <fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>.
}

REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0072617
|Bernstein and Cline
|1994
REFM|FBrf0076149
|Pultz and Baker
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014234	ICL 1 P	SYM 1 P{}Sxl<up>fPODH</up>	ASTR 1 -	CLOC 1 6F3--5	REF 1 2	DT 1 6 Jan 2000	RESZ 439
ID|FBti0014234
SYM|P{}Sxl<up>fPODH</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0046351
|Salz et al.
|1987
SYN|P{}Sxl<up>fPODH</up>
ASAL|<fbsym>FBal0016699==Sxl<up>fPODH</up></fbsym>
CLOC|6F3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003659==Sxl</fbsym>
}

REF
{
REFM|FBrf0046351
|Salz et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016699==Sxl<up>fPODH</up></fbsym>

REFDSR
{
RDID|FBrf0046351
|Salz et al.
|1987
PHP|Fails to complement <fbsym>FBgn0003659==Sxl</fbsym> alleles that are defective in somatic function,
|suggesting that this allele probably eliminates all known somatic functions.
|Partially complements <fbsym>FBal0016681==Sxl<up>f2</up></fbsym>, an allele defective in
| germline function;
|heteroallelic females are semi-fertile and the ovaries do not contain
|any abnormal oocytes.
}

REF
{
REFM|FBrf0046351
|Salz et al.
|1987
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014235	ICL 1 P	SYM 1 P{}Sxl<up>fPb</up>	ASTR 1 -	CLOC 1 6F3--5	REF 1 3	DT 1 6 Jan 2000	RESZ 491
ID|FBti0014235
SYM|P{}Sxl<up>fPb</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0042036
|Maine et al.
|1985
SYN|P{}Sxl<up>fPb</up>
ASAL|<fbsym>FBal0016696==Sxl<up>fPb</up></fbsym>
CLOC|6F3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003659==Sxl</fbsym>
PHC|lethal | female
}

REF
{
REFM|FBrf0042036
|Maine et al.
|1985
REFM|FBrf0046351
|Salz et al.
|1987
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016696==Sxl<up>fPb</up></fbsym>

REFDSR
{
RDID|FBrf0046351
|Salz et al.
|1987
PHP|Partial loss-of-function allele. Only partially complemented by <fbsym>FBal0016685==Sxl<up>f7,M1</up></fbsym>.
|Fully complements <fbsym>FBal0016686==Sxl<up>f9</up></fbsym> and
| <fbsym>FBal0016681==Sxl<up>f2</up></fbsym>. Homozygous germline clones
|develop normally.
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|A P-insertion-induced lethal hypomorphic allele with the unusual
|distinction of displaying a mosaic intersex phenotype in homozygous
|mutant diplo-X clones induced by mitotic recombination; hence, appears
|to be defective in the cellular maintenance of the female sexual
|commitment. Under dysgenic conditions, can mutate further to less
|extreme or to more extreme condition. Partially complements
|<fbsym>FBal0016685==Sxl<up>f7,M1</up></fbsym>, generating masculinized individuals; partially
|... (see <fbsym>FBal0016696==Sxl<up>fPb</up></fbsym> report)
}

REF
{
REFM|FBrf0046351
|Salz et al.
|1987
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014236	ICL 1 ?	SYM 1 ?{}Sxl<up>fc</up>	ASTR 1 -	CLOC 1 6F3--5	REF 1 2	DT 1 6 Jan 2000	RESZ 441
ID|FBti0014236
SYM|?{}Sxl<up>fc</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
SYN|?{}Sxl<up>fc</up>
ASAL|<fbsym>FBal0030317==Sxl<up>fc</up></fbsym>
CLOC|6F3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003659==Sxl</fbsym>
PHC|lethal | recessive | female | partially
}

REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030317==Sxl<up>fc</up></fbsym>

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHP|Fully complements <fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>. Homozygous females show a
| high degree
|of lethality; 70% die as embryos, 28% die as larvae. Those that survive
|are normal females. Homozygous clones also develop female structures.
|Homozygous germ cell clones give rise to functional eggs. <fbsym>FBal0016685==Sxl<up>f7,M1</up></fbsym>/<fbsym>FBal0030317==Sxl<up>fc</up></fbsym>
|flies lack gonads and occasionally have a male spot on the fifth and
|sixth tergites. Viability is greatly reduced in heterozygous combination
|with <fbsym>FBab0000599==Df(1)N71</fbsym> or <fbsym>FBab0000974==Df(1)svr</fbsym>.
}

REFDSR
{
RDID|FBrf0058121
|Granadino et al.
|1993
PHP|<fbsym>FBal0016685==Sxl<up>f7,M1</up></fbsym>/<fbsym>FBal0030317==Sxl<up>fc</up></fbsym> females do
| not develop ovaries, though germ
|cells of this genotype transplanted into wild-type hosts produce functional
|oocytes, suggesting that it is in the somatic cells of this genotype
|that the ovaries are affected.
PHM|ovary
}

REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0058121
|Granadino et al.
|1993
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014241	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bx-AF</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 6 Jan 2000	RESZ 460
ID|FBti0014241
SYM|gypsy{}Ubx<up>bx-AF</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|gypsy{}Ubx<up>bx-AF</up>
ASAL|<fbsym>FBal0017523==Ubx<up>bx-AF</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014246	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bx-X</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 6 Jan 2000	RESZ 457
ID|FBti0014246
SYM|gypsy{}Ubx<up>bx-X</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|gypsy{}Ubx<up>bx-X</up>
ASAL|<fbsym>FBal0017531==Ubx<up>bx-X</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014248	ICL 1 gypsy	SYM 1 gypsy{}Ubx<up>bxd-PR</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 6 Jan 2000	RESZ 459
ID|FBti0014248
SYM|gypsy{}Ubx<up>bxd-PR</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0049522
|Harrison et al.
|1989
SYN|gypsy{}Ubx<up>bxd-PR</up>
ASAL|<fbsym>FBal0028588==Ubx<up>bxd-PR</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
}

REF
{
REFM|FBrf0049522
|Harrison et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0028588==Ubx<up>bxd-PR</up></fbsym>

REFDSR
{
RDID|FBrf0049522
|Harrison et al.
|1989
PHP|Partial revertant.
}

REF
{
REFM|FBrf0049522
|Harrison et al.
|1989
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014249	ICL 1 ?	SYM 1 ?{}Ubx<up>bxd-SR</up>	ASTR 1 -	CLOC 1 89D6--9	REF 1 2	DT 1 6 Jan 2000	RESZ 404
ID|FBti0014249
SYM|?{}Ubx<up>bxd-SR</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003944==Ubx</fbsym>

REFDSR
{
RDID|FBrf0040194
|Bender et al.
|1983
SYN|?{}Ubx<up>bxd-SR</up>
ASAL|<fbsym>FBal0017560==Ubx<up>bxd-SR</up></fbsym>
CLOC|89D6--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003944==Ubx</fbsym>
}

REF
{
REFM|FBrf0040194
|Bender et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014256	ICL 1 P	SYM 1 P{}aop<up>yan-AM</up>	ASTR 1 -	CLOC 1 22D1	REF 1 2	DT 1 6 Jan 2000	RESZ 446
ID|FBti0014256
SYM|P{}aop<up>yan-AM</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000097==aop</fbsym>

REFDSR
{
RDID|FBrf0072711
|Brunner et al.
|1994
SYN|P{}aop<up>yan-AM</up>
ASAL|<fbsym>FBal0034186==aop<up>yan-AM</up></fbsym>
CLOC|22D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000097==aop</fbsym>
}

REF
{
REFM|FBrf0072711
|Brunner et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014268	ICL 1 ?	SYM 1 ?{}bt<up>l-a</up>	ASTR 1 -	CLOC 1 102C2--3	REF 1 4	DT 1 6 Jan 2000	RESZ 780
ID|FBti0014268
SYM|?{}bt<up>l-a</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0005666==bt</fbsym>

REFDSR
{
RDID|FBrf0016176
|Hochman et al.
|1964
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0022724
|Hochman
|1971
PHC|lethal
}

REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
SYN|?{}bt<up>l-a</up>
ASAL|<fbsym>FBal0027983==bt<up>l-a</up></fbsym>
CLOC|102C2--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005666==bt</fbsym>
PHC|lethal | embryonic stage | recessive
|(with bt<up>D</up>) lethal | embryonic stage
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0016176
|Hochman et al.
|1964
REFM|FBrf0022724
|Hochman
|1971
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0027983==bt<up>l-a</up></fbsym>

REFDSR
{
RDID|FBrf0079869
|Ayme-Southgate et al.
|1995
PHP|Homozygotes die as late embryos and do not have spontaneous muscle
|contractions. <fbsym>FBal0001328==bt<up>D</up></fbsym>/<fbsym>FBal0027983==bt<up>l-a</up></fbsym>
| transheterozygotes die as embryos.
}

REF
{
REFM|FBrf0079869
|Ayme-Southgate et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014271	ICL 1 P	SYM 1 P{}cact<up>BQ</up>	ASTR 1 -	CLOC 1 35F1	REF 1 4	DT 1 6 Jan 2000	RESZ 510
ID|FBti0014271
SYM|P{}cact<up>BQ</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000250==cact</fbsym>

REFDSR
{
RDID|FBrf0053786
|Roth et al.
|1991
SYN|P{}cact<up>BQ</up>
ASAL|<fbsym>FBal0030692==cact<up>BQ</up></fbsym>
CLOC|35F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000250==cact</fbsym>
}

REF
{
REFM|FBrf0053786
|Roth et al.
|1991
REFM|FBrf0092467
|Bergmann et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0150746
|Kiger and Ho
|2001
}

ALESR
{
ASYM|<fbsym>FBal0030692==cact<up>BQ</up></fbsym>

REFDSR
{
RDID|FBrf0053786
|Roth et al.
|1991
PHP|When in trans to loss-of-function cact alleles a dorsalized embryo
|is generated.
}

REFDSR
{
RDID|FBrf0058074
|Govind et al.
|1993
PHP|Females homozygous for this allele or heterozygous for this allele
|and a deficiency for <fbsym>FBgn0000250==cact</fbsym> generate strongly dorsalized or dorsolateralized
|embryos. Females transheterozygous for this allele and a loss of function
|allele result in embryos in which ventral structures are progressively
|lost at the expense of dorsal structures as the strength of the loss
|of function allele increases.
PHM|embryonic ventral epidermis
}

REFDSR
{
RDID|FBrf0092467
|Bergmann et al.
|1996
PHP|Causes a dorsalized phenotype.
PHM|embryonic/first instar larval cuticle | ventral
}

REFDSR
{
RDID|FBrf0103015
|Qiu et al.
|1998
PHP|No <fbsym>FBal0001509==cact<up>3</up></fbsym>/<fbsym>FBal0030692==cact<up>BQ</up></fbsym>;
| <fbsym>FBal0016828==Tl<up>3</up></fbsym>/+ adults or <fbsym>FBal0001509==cact<up>3</up></fbsym>/<fbsym>FBal0030692==cact<up>BQ</up></fbsym>
|; <fbsym>FBal0016833==Tl<up>8</up></fbsym>/+ adults have melanotic capsules.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHM|embryonic ventral epidermis
}

REF
{
REFM|FBrf0053786
|Roth et al.
|1991
REFM|FBrf0058074
|Govind et al.
|1993
REFM|FBrf0092467
|Bergmann et al.
|1996
REFM|FBrf0103015
|Qiu et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014283	ICL 1 ?	SYM 1 ?{}ci<up>W</up>	ASTR 1 -	CLOC 1 102A1--3	REF 1 2	DT 1 6 Jan 2000	RESZ 439
ID|FBti0014283
SYM|?{}ci<up>W</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0004859==ci</fbsym>
SK|FBst0000646
|ci[W]
|Total=1

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|?{}ci<up>W</up>
ASAL|<fbsym>FBal0001653==ci<up>W</up></fbsym>
MU|spontaneous
CLOC|102A1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004859==ci</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0001653==ci<up>W</up></fbsym>

REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Lack all longitudinal and transverse veins and affect morphogenesis
|of legs and eyes.
}

REFDSR
{
RDID|FBrf0073755
|Locke and Tartof
|1994
PHP|Homozygous viable.
}

REFDSR
{
RDID|FBrf0087686
|Sanchez-Herrero et al.
|1996
PHP|Homozygotes occasionally show overgrowth in the anterior compartment
|of the wing. <fbsym>FBal0001651==ci<up>D</up></fbsym>/<fbsym>FBal0001653==ci<up>W</up></fbsym> flies
| have abnormal legs.
PHM|wing | anterior compartment
|(with ci<up>D</up>) leg
}

REFDSR
{
RDID|FBrf0088080
|Dominguez et al.
|1996
PHP|Wings from homozygotes have, at low penetrance, a mirror symmetrical
|outgrowth composed of anterior wing material, resembling duplications
|caused by ectopic <fbsym>FBgn0000490==dpp</fbsym> expression.
PHM|wing
}

REFDSR
{
RDID|FBrf0092613
|Locke and Hanna
|1996
PHM|wing vein
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Homozygote is extreme ci type. Wings sometimes almost
|twice normal width, arclike, and virtually lack veins.
|Often present is a well-organized pattern of venation
|in which the posterior crossvein flows smoothly into
|L5. Legs lumpy, sex combs larger than normal, antennae
|enlarged, eyes smaller and extra bristles present.
|Heterozygote shows gap in L4 in 80% of flies. <fbsym>FBal0001653==ci<up>W</up></fbsym>
|... (see <fbsym>FBal0001653==ci<up>W</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0108513
|Dominguez
|1999
PHP|When analyzed in large clones in the developing eye the packing in
|the ommatidial clusters is disrupted.
PHM|ommatidial cluster
}

REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|Heterozygotes show variable loss of vein L4 tissue.
PHM|wing vein L4
}

REFDSR
{
RDID|FBrf0130102
|Svendsen et al.
|2000
PHP|Heterozygotes show wing vein L4 defects.
PHM|wing vein L4
}

REF
{
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0073755
|Locke and Tartof
|1994
REFM|FBrf0087686
|Sanchez-Herrero et al.
|1996
REFM|FBrf0088080
|Dominguez et al.
|1996
REFM|FBrf0092613
|Locke and Hanna
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108513
|Dominguez
|1999
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
REFM|FBrf0130102
|Svendsen et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014288	ICL 1 jockey	SYM 1 jockey{}ct<up>+D</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 2	DT 1 6 Jan 2000	RESZ 443
ID|FBti0014288
SYM|jockey{}ct<up>+D</up>
ASTP|<fbsym>FBtp0011444==jockey</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|jockey
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0052591
|Flavell et al.
|1990
SYN|jockey{}ct<up>+D</up>
ASAL|<fbsym>FBal0030974==ct<up>+D</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0052591
|Flavell et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030974==ct<up>+D</up></fbsym>

REFDSR
{
RDID|FBrf0052591
|Flavell et al.
|1990
PHP|Complete reversion to wild type.
}

REF
{
REFM|FBrf0052591
|Flavell et al.
|1990
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014295	ICL 1 gypsy	SYM 1 gypsy{}ct<up>K</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 8	DT 1 6 Jan 2000	RESZ 946
ID|FBti0014295
SYM|gypsy{}ct<up>K</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0004198==ct</fbsym>
SK|FBst0000171
|y[1] ct[K]; bw[1]
|Total=1

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|gypsy{}ct<up>K</up>
ASAL|<fbsym>FBal0002000==ct<up>K</up></fbsym>
MU|spontaneous
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REFDSR
{
RDID|FBrf0053813
|Jack et al.
|1991
PHC|lethal | larval stage | recessive
}

REFDSR
{
RDID|FBrf0054133
|Liu et al.
|1991
PHC|lethal
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|lethal
}

REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0053813
|Jack et al.
|1991
REFM|FBrf0054133
|Liu et al.
|1991
REFM|FBrf0056247
|Hoover et al.
|1992
REFM|FBrf0098327
|Ponomarenko et al.
|1997
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002000==ct<up>K</up></fbsym>

REFDSR
{
RDID|FBrf0033190
|Johnson and Judd
|1979
PHP|Scalloped wings. Bristles are finer than wild-type. Completely complemented
|by <fbsym>FBab0000623==Df(1)R19</fbsym>.
PHM|wing
|macrochaeta
}

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Flies have scalloped wing margins and fine scutellar bristles.
PHM|wing
|scutellar bristle
}

REFDSR
{
RDID|FBrf0053813
|Jack et al.
|1991
PHP|Adult survivors exhibit wing margin defects.
PHM|Malpighian tubule
|adult spiracle
|external sensory organ
|central nervous system
|vibrissae
|wing
}

REFDSR
{
RDID|FBrf0054133
|Liu et al.
|1991
PHP|Homozygous embryos lack Malpighian tubules and the gut wall is 3--4
|fold thicker than wild type at the junction of the posterior and anterior
|midgut.
}

REFDSR
{
RDID|FBrf0063599
|Krivshenko
|1956
PHP|Mutants have a number of cuts on the internal and external sides of
|the wing (resembling <fbsym>FBgn0003345==sd</fbsym> mutations). The macrochaetae of the mesonotum
|and especially the scutellum are of the M type.
PHM|wing
|scutum & macrochaeta
|scutellum & macrochaeta
}

REFDSR
{
RDID|FBrf0102837
|Johnston et al.
|1998
PHP|Shows no interaction with <fbsym>FBgn0051481==pb</fbsym> mutations.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|cut wings
|fine bristles
|Classified as a group-I lethal because
|homozygotes show reduced viability and only 10% of
|fewer heterozygotes with other lethal alleles survive;
|survivors have weakly cut wings, as well as fine
|bristles and enlarged and deformed humeral callus, not
|... (see <fbsym>FBal0002000==ct<up>K</up></fbsym> report)
}

REF
{
REFM|FBrf0033190
|Johnson and Judd
|1979
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0053813
|Jack et al.
|1991
REFM|FBrf0054133
|Liu et al.
|1991
REFM|FBrf0063599
|Krivshenko
|1956
REFM|FBrf0102837
|Johnston et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014345	ICL 1 roo	SYM 1 roo{}ct<up>MRP</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 3	DT 1 6 Jan 2000	RESZ 479
ID|FBti0014345
SYM|roo{}ct<up>MRP</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0050561
|Tchurikov et al.
|1989
SYN|roo{}ct<up>MRP</up>
ASAL|<fbsym>FBal0002073==ct<up>MRP</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014363	ICL 1 jockey	SYM 1 jockey{}ct<up>MRpD</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 2	DT 1 6 Jan 2000	RESZ 492
ID|FBti0014363
SYM|jockey{}ct<up>MRpD</up>
ASTP|<fbsym>FBtp0011444==jockey</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|jockey
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0052591
|Flavell et al.
|1990
SYN|jockey{}ct<up>MRpD</up>
ASAL|<fbsym>FBal0030974==ct<up>+D</up></fbsym>
|<fbsym>FBal0030987==ct<up>MRpD</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0052591
|Flavell et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0030974==ct<up>+D</up></fbsym>

REFDSR
{
RDID|FBrf0052591
|Flavell et al.
|1990
PHP|Complete reversion to wild type.
}

REF
{
REFM|FBrf0052591
|Flavell et al.
|1990
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0030987==ct<up>MRpD</up></fbsym>

REFDSR
{
RDID|FBrf0052591
|Flavell et al.
|1990
PHP|Weak cut wing phenotype.
PHM|wing
}

REF
{
REFM|FBrf0052591
|Flavell et al.
|1990
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014382	ICL 1 gypsy	SYM 1 gypsy{}ct<up>MRwR</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 2	DT 1 6 Jan 2000	RESZ 451
ID|FBti0014382
SYM|gypsy{}ct<up>MRwR</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|gypsy{}ct<up>MRwR</up>
ASAL|<fbsym>FBal0002092==ct<up>MRwR</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002092==ct<up>MRwR</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Cut wings.
PHM|wing
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014392	ICL 1 roo	SYM 1 roo{}ct<up>n</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 4	DT 1 6 Jan 2000	RESZ 816
ID|FBti0014392
SYM|roo{}ct<up>n</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0004198==ct</fbsym>
SK|FBst0000024
|ct[n] oc[1]/FM1
|FBst0002550
|C(1)M4, y[2]/ct[n] oc[1] Hmr[1] v[1]
|FBst0003022
|ct[n] otu[1] v[24]/FM3
|FBst0004093
|C(1)RM, In(1)dl-49, y[1] ct[l] sn[X2]: y[1] <fbsym>FBal0002094==ct[n]</fbsym> oc[1] ptg[1] car[1]/R(YL)/C(1;YS)1, oc[1] ptg[1]
|Total=4

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|roo{}ct<up>n</up>
ASAL|<fbsym>FBal0002094==ct<up>n</up></fbsym>
MU|heat-treatment
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0050561
|Tchurikov et al.
|1989
REFM|FBrf0098741
|Tchurikov et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002094==ct<up>n</up></fbsym>

REFDSR
{
RDID|FBrf0033190
|Johnson and Judd
|1979
PHP|Notched wings. Completely complemented by <fbsym>FBab0000623==Df(1)R19</fbsym>.
PHM|wing
}

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Phenotype is unaffected by <fbsym>FBal0032166==mod(mdg4)<up>ul</up></fbsym>.
}

REFDSR
{
RDID|FBrf0053813
|Jack et al.
|1991
PHP|Adult wing margin has gaps at the tip.
PHM|wing
}

REFDSR
{
RDID|FBrf0063799
|Plough and Ives
|1934
PHP|Phenotype is much less extreme than <fbsym>FBal0001933==ct<up>1</up></fbsym>. Shallow
| terminal notches
|are seen between wing veins L2 and L3 and between veins L3 and L4.
|Some variation in the phenotype is seen.
| <fbsym>FBal0002094==ct<up>n</up></fbsym>/<fbsym>FBal0001933==ct<up>1</up></fbsym> flies have
|the same phenotype as <fbsym>FBal0002094==ct<up>n</up></fbsym> homozygotes.
PHM|wing
}

REFDSR
{
RDID|FBrf0098380
|de Celis and Bray
|1997
PHP|Severe allele that produces extensive loss of wing margin structures.
PHM|wing
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|cut wings
|Wings notched at tips. Classification of males reliable, of
|females harder, but perfect at higher temperatures. Viability
|excellent.
|RK1 in male.
}

REF
{
REFM|FBrf0033190
|Johnson and Judd
|1979
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0053813
|Jack et al.
|1991
REFM|FBrf0063799
|Plough and Ives
|1934
REFM|FBrf0098380
|de Celis and Bray
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014394	ICL 1 copia	SYM 1 copia{}ct<up>ns</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 2	DT 1 6 Jan 2000	RESZ 451
ID|FBti0014394
SYM|copia{}ct<up>ns</up>
ASTP|<fbsym>FBtp0011420==copia</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|copia
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
SYN|copia{}ct<up>ns</up>
ASAL|<fbsym>FBal0002095==ct<up>ns</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002095==ct<up>ns</up></fbsym>

REFDSR
{
RDID|FBrf0033190
|Johnson and Judd
|1979
PHP|Notched wings.
PHM|wing
}

REFDSR
{
RDID|FBrf0053813
|Jack et al.
|1991
PHP|Adult wing margin has gaps at the tip.
PHM|wing
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|weak allele
}

REF
{
REFM|FBrf0033190
|Johnson and Judd
|1979
REFM|FBrf0053813
|Jack et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014408	ICL 1 roo	SYM 1 roo{}dsx<up>D</up>	ASTR 1 -	CLOC 1 84E5--6	REF 1 3	DT 1 6 Jan 2000	RESZ 941
ID|FBti0014408
SYM|roo{}dsx<up>D</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0000504==dsx</fbsym>
SK|FBst0000840
|T(1;3)OR60/TM2/In(3R)C, <fbsym>FBal0003200==dsx[D]</fbsym> Sb[1] sprd[1] e[1] l(3)e[1]
|FBst0001141
|C(1)RM, y[2] sc[1] z[1]/T(1;3)m9, <fbsym>FBal0003200==dsx[D]</fbsym> Sb[1] e[1] l(3)e[1]
|FBst0002451
|st[1] betaTub85D[D] ss[1] e[s]/TM2 & <fbsym>FBal0003200==dsx[D]</fbsym> Sb[1] e[1]/TM2
|FBst1000043
|B[S] Y; T(1;3)OR60, y; <fbsym>FBal0003200==dsx[D]</fbsym> Sb e/ TM6
|FBst1000044
|B[S] Y; T(1;3)OR60; dsx[D]/ TM8
|Total=5

REFDSR
{
RDID|FBrf0051864
|Nagoshi and Baker
|1990
SYN|roo{}dsx<up>D</up>
ASAL|<fbsym>FBal0003200==dsx<up>D</up></fbsym>
MU|spontaneous
CLOC|84E5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000504==dsx</fbsym>
}

REF
{
REFM|FBrf0051864
|Nagoshi and Baker
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003200==dsx<up>D</up></fbsym>

REFDSR
{
RDID|FBrf0027527
|Duncan and Kaufman
|1975
PHP|Female intersexuals.
}

REFDSR
{
RDID|FBrf0037844
|Schupbach
|1982
PHP|Effects only XX flies. Homozygous XX flies have rudimentary gonads,
|occasionally with some oocytes and eggs.
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/<fbsym>FBal0003154==dsx<up>1</up></fbsym> flies are
|transformed into somatically male-like animals.
}

REFDSR
{
RDID|FBrf0039215
|Epper and Sanchez
|1983
PHP|Flies are intersex, having two somewhat abnormal and incomplete sets
|of genitalia.
}

REFDSR
{
RDID|FBrf0046300
|Nothiger et al.
|1987
PHP|Only affects XX flies: the terminalia of XX heterozygous flies carry
|abnormal male and female elements, with the female genitalia anterior
|to the male genitalia. The male genitalia are well developed, but
|the penis apparatus is reduced, the hypandrium is mostly absent and
|many bristles are abnormal. The female vaginal plate is always present,
|but is reduced in size with abnormal bristles. There is often a mass
|of yellow, chitinized material between the vaginal plates, which is
|... (see <fbsym>FBal0003200==dsx<up>D</up></fbsym> report)
PHM|female terminalia
|female genitalia
|female gonopod
|prothoracic leg | female
|female analia
|anal plate | female
}

REFDSR
{
RDID|FBrf0049556
|Nothiger et al.
|1989
PHP|They are sterile even in the presence of a Y chromosome. The gonads
|form testes which are generally non-gametogenic, containing degenerated
|germ cells and debris or gonial cells whose sex cannot be determined.
|A variable proportion are gametogenic, containing either oogenic or
|spermatogenic stages of germ cell development (never both in the same
|gonad). In these cases oogenesis is arrested anywhere between stages
|... (see <fbsym>FBal0003200==dsx<up>D</up></fbsym> report)
PHM|gonad
}

REFDSR
{
RDID|FBrf0053736
|Feng et al.
|1991
PHP|Heterozygous flies are intersex, having both male and female reproductive
|organs.
PHM|genitalia
}

REFDSR
{
RDID|FBrf0055047
|Hilfiker and Nothiger
|1991
PHP|<fbsym>FBal0018011==vir<up>ts</up></fbsym>/<fbsym>FBal0018011==vir<up>ts</up></fbsym>
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ XX flies have a <fbsym>FBgn0000504==dsx</fbsym> phenotype at 25<up>o</up>C,
|and are strongly masculinized intersexes or almost pseudomales with
|poorly developed gonads at 29<up>o</up>C.
}

REFDSR
{
RDID|FBrf0055884
|Taylor and Truman
|1992
PHP|Sex specific neuroblasts fail to undergo any postembryonic divisions
|in male or female larval nervous systems.
}

REFDSR
{
RDID|FBrf0074590
|Taylor et al.
|1994
PHP|XX <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+,
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/<fbsym>FBab0002755==Df(3R)dsx15</fbsym> and
| <fbsym>FBal0005628==ix<up>1</up></fbsym>/<fbsym>FBal0005628==ix<up>1</up></fbsym>; <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+
|flies do not show any male-specific courtship when paired with mature
|virgin females.
|88% of XY <fbsym>FBal0003200==dsx<up>D</up></fbsym>/<fbsym>FBab0002755==Df(3R)dsx15</fbsym> flies,
| 100% of XY <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ flies
|and 50% of XY <fbsym>FBal0005628==ix<up>1</up></fbsym>/<fbsym>FBal0005628==ix<up>1</up></fbsym>;
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ flies show male-specific
|courtship when paired with mature virgin females.
}

REFDSR
{
RDID|FBrf0089694
|Humphreys et al.
|1996
PHP|<fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ and
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/<fbsym>FBal0062879==dsx<up>3-A135</up></fbsym> adults are
| hypersensitive to
|paraquat.
}

REFDSR
{
RDID|FBrf0090773
|Rudner et al.
|1996
PHP|<fbsym>FBal0003200==dsx<up>D</up></fbsym> is unable to suppress the sex comb defect seen
| in homozygous
|male <fbsym>FBal0008116==U2af38<up>06751</up></fbsym> flies.
}

REFDSR
{
RDID|FBrf0092518
|Finley et al.
|1997
PHP|XX <fbsym>FBal0045531==dsf<up>1</up></fbsym> <fbsym>FBal0003200==dsx<up>D</up></fbsym> double
| hemizygotes have wild-type ventral abdominal
|muscle innervation phenotype, while XY <fbsym>FBgn0015381==dsf</fbsym><up>+</up> <fbsym>FBgn0003741==tra</fbsym><up>-</up>
| <fbsym>FBal0045531==dsf<up>1</up></fbsym> <fbsym>FBal0003200==dsx<up>D</up></fbsym>
|double hemizygotes have a <fbsym>FBal0045531==dsf<up>1</up></fbsym> ventral abdominal
| muscle innervation
|phenotype, indicating that <fbsym>FBgn0015381==dsf</fbsym> acts independently of <fbsym>FBgn0000504==dsx</fbsym>.
}

REFDSR
{
RDID|FBrf0098342
|Sanchez and Santamaria
|1997
PHP|XX D.teissieri-D.melanogaster hybrid flies carrying one copy of <fbsym>FBal0003200==dsx<up>D</up></fbsym>
|have an almost completely normal set of male genital structures. Vaginal
|plates are almost always absent and the female eighth tergite is incomplete
|or missing. The penis apparatus is more normal in terms of the structures
|present and their differentiation in XX D.teissieri-D.melanogaster
|<fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ hybrid flies than in XX D.melanogaster
| <fbsym>FBal0003200==dsx<up>D</up></fbsym>/+ flies.
|The seventh tergite and sternite are present in XX D.melanogaster
|... (see <fbsym>FBal0003200==dsx<up>D</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0105191
|Arthur et al.
|1998
PHP|X/X <fbsym>FBal0017004==tra<up>1</up></fbsym>/<fbsym>FBal0017004==tra<up>1</up></fbsym>
| <fbsym>FBal0051045==tra<up>hs.PBa</up></fbsym> and X/Y
| <fbsym>FBal0017004==tra<up>1</up></fbsym>/<fbsym>FBal0017004==tra<up>1</up></fbsym> <fbsym>FBal0051045==tra<up>hs.PBa</up></fbsym>
|flies have a female body and pheromone pattern and display indiscriminate
|sexual behavior. By introducing <fbsym>FBal0003200==dsx<up>D</up></fbsym> mutants now
| have a male
|body and male pheromone pattern, these flies are unattractive to males
|but will still court both sexes.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|dominant; affects XX only
}

REFDSR
{
RDID|FBrf0162055
|DeFalco et al.
|2003
PHP|Female <fbsym>FBal0003200==dsx<up>D</up></fbsym>/<fbsym>FBal0003154==dsx<up>1</up></fbsym> stage 15
| gonads exhibit a completely masculinized
|phenotype, in which male-specific somatic gonadal precursors are clearly
|present.
PHM|(with dsx<up>1</up>) gonadal sheath proper primordium | female
}

REF
{
REFM|FBrf0027527
|Duncan and Kaufman
|1975
REFM|FBrf0037844
|Schupbach
|1982
REFM|FBrf0039215
|Epper and Sanchez
|1983
REFM|FBrf0046300
|Nothiger et al.
|1987
REFM|FBrf0049556
|Nothiger et al.
|1989
REFM|FBrf0053736
|Feng et al.
|1991
REFM|FBrf0055047
|Hilfiker and Nothiger
|1991
REFM|FBrf0055884
|Taylor and Truman
|1992
REFM|FBrf0074590
|Taylor et al.
|1994
REFM|FBrf0089694
|Humphreys et al.
|1996
REFM|FBrf0090773
|Rudner et al.
|1996
REFM|FBrf0092518
|Finley et al.
|1997
REFM|FBrf0098342
|Sanchez and Santamaria
|1997
REFM|FBrf0105191
|Arthur et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0162055
|DeFalco et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014409	ICL 1 F	SYM 1 F{}dsx<up>M</up>	ASTR 1 -	CLOC 1 84E5--6	REF 1 3	DT 1 6 Jan 2000	RESZ 573
ID|FBti0014409
SYM|F{}dsx<up>M</up>
ASTP|<fbsym>FBtp0011425==F-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|F
ASGN|<fbsym>FBgn0000504==dsx</fbsym>
SK|FBst0004243
|dsx[M]/In(3L)P, In(3R)P, Me[1]/Dp(1;3)B[S3i], B[+]
|Total=1

REFDSR
{
RDID|FBrf0051864
|Nagoshi and Baker
|1990
SYN|F{}dsx<up>M</up>
ASAL|<fbsym>FBal0003202==dsx<up>M</up></fbsym>
MU|spontaneous
CLOC|84E5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000504==dsx</fbsym>
}

REF
{
REFM|FBrf0051864
|Nagoshi and Baker
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003202==dsx<up>M</up></fbsym>

REFDSR
{
RDID|FBrf0046300
|Nothiger et al.
|1987
PHP|Only affects XX flies: the terminalia of XX heterozygous flies carry
|abnormal male and female elements, with the female genitalia anterior
|to the male genitalia. The male genitalia are well developed, but
|the penis apparatus is reduced, the hypandrium is mostly absent and
|many bristles are abnormal. The female vaginal plate is always present,
|but is reduced in size with abnormal bristles. There is often a mass
|of yellow, chitinized material between the vaginal plates, which is
|... (see <fbsym>FBal0003202==dsx<up>M</up></fbsym> report)
PHM|female terminalia
|female genitalia
|female gonopod
|prothoracic leg | female
|female analia
|anal plate | female
|genitalia
}

REFDSR
{
RDID|FBrf0049556
|Nothiger et al.
|1989
PHP|Chromosomal females (XX) mutant for <fbsym>FBgn0000504==dsx</fbsym> are transformed into "pseudomales".
|They are sterile even in the presence of a Y chromosome. The gonads
|form testes.
PHM|gonad
}

REFDSR
{
RDID|FBrf0055884
|Taylor and Truman
|1992
PHP|Sex specific neuroblasts fail to undergo any postembryonic divisions
|in male or female larval nervous systems.
}

REFDSR
{
RDID|FBrf0074590
|Taylor et al.
|1994
PHP|XX <fbsym>FBal0003202==dsx<up>M</up></fbsym>/+ flies do not show any male-specific
| courtship when paired
|with mature virgin females.
|100% of XY <fbsym>FBal0003202==dsx<up>M</up></fbsym>/+ flies show male-specific courtship
| when paired
|with mature virgin females.
}

REFDSR
{
RDID|FBrf0080396
|Simmerl et al.
|1995
PHP|Intersex phenotype. Cells derived from the female genital disc can
|develop male genital structures.
PHM|genital disc
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|dominant; affects XX only
}

REFDSR
{
RDID|FBrf0134558
|Sanchez et al.
|2001
PHP|<fbsym>FBal0003202==dsx<up>M</up></fbsym>/+ genital discs are intersexual; both male and
| female genital
|primordia develop in these discs.
PHM|genital disc
}

REF
{
REFM|FBrf0046300
|Nothiger et al.
|1987
REFM|FBrf0049556
|Nothiger et al.
|1989
REFM|FBrf0055884
|Taylor and Truman
|1992
REFM|FBrf0074590
|Taylor et al.
|1994
REFM|FBrf0080396
|Simmerl et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0134558
|Sanchez et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014410	ICL 1 ?	SYM 1 ?{}dsx<up>T</up>	ASTR 1 -	CLOC 1 84E5--6	REF 1 3	DT 1 6 Jan 2000	RESZ 454
ID|FBti0014410
SYM|?{}dsx<up>T</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0000504==dsx</fbsym>

REFDSR
{
RDID|FBrf0051864
|Nagoshi and Baker
|1990
SYN|?{}dsx<up>T</up>
ASAL|<fbsym>FBal0003205==dsx<up>T</up></fbsym>
MU|spontaneous
CLOC|84E5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000504==dsx</fbsym>
}

REF
{
REFM|FBrf0051864
|Nagoshi and Baker
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003205==dsx<up>T</up></fbsym>

REFDSR
{
RDID|FBrf0046300
|Nothiger et al.
|1987
PHP|Only affects XX flies: the terminalia of XX heterozygous flies carry
|abnormal male and female elements, with the female genitalia anterior
|to the male genitalia. The male genitalia are well developed, but
|the penis apparatus is reduced, the hypandrium is mostly absent and
|many bristles are abnormal. The female vaginal plate is always present,
|but is reduced in size with abnormal bristles. There is often a mass
|of yellow, chitinized material between the vaginal plates, which is
|... (see <fbsym>FBal0003205==dsx<up>T</up></fbsym> report)
PHM|female terminalia
|female genitalia
|female gonopod
|prothoracic leg | female
|female analia
|anal plate | female
|genitalia
}

REFDSR
{
RDID|FBrf0076142
|Nagoshi et al.
|1995
PHP|No more than 26% of XX
| <fbsym>FBal0003205==dsx<up>T</up></fbsym>/<fbsym>FBal0003154==dsx<up>1</up></fbsym> mutant
| pseudomales produce
|gonads with the most severe group 1 pseudotestes phenotype. The remaining
|pseudomales have a less severe phenotype, with viable germ cells.
|<fbsym>FBal0013357==otu<up>10</up></fbsym> and <fbsym>Df(1)otu-P&Dgr;1</fbsym> cause an increase in
| severity of
|this phenotype: over 70% of the resulting gonads were of group 1.
PHM|germ cell
}

REF
{
REFM|FBrf0046300
|Nothiger et al.
|1987
REFM|FBrf0076142
|Nagoshi et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014411	ICL 1 P	SYM 1 P{}dx<up>P</up>	ASTR 1 -	CLOC 1 6B1--2	REF 1 2	DT 1 6 Jan 2000	RESZ 428
ID|FBti0014411
SYM|P{}dx<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000524==dx</fbsym>

REFDSR
{
RDID|FBrf0068437
|Busseau et al.
|1994
SYN|P{}dx<up>P</up>
ASAL|<fbsym>FBal0031146==dx<up>P</up></fbsym>
CLOC|6B1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000524==dx</fbsym>
}

REF
{
REFM|FBrf0068437
|Busseau et al.
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031146==dx<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0051969
|Xu and Artavanis-Tsakonas
|1990
PHP|Viable. Extra wing vein material at tips. Weak rough eye phenotype:
|irregular ommatidia, bristles are duplicated or missing. No visual
|abnormality.
}

REFDSR
{
RDID|FBrf0068437
|Busseau et al.
|1994
PHM|wing
|eye
|ocellus
}

REFDSR
{
RDID|FBrf0141440
|Ramain et al.
|2001
PHP|Homozygous females have an excess of microchaetae, having 143.00 +/-
|1.92 thoracic microchaetae per heminotum (compared to the wild-type
|number of 130.35 +/- 1.54).
PHM|microchaeta
}

REFDSR
{
RDID|FBrf0151854
|Duvic et al.
|2002
PHP|<fbsym>FBal0031146==dx<up>P</up></fbsym> mutant larvae have normal wild-type numbers of
| crystal cells.
}

REF
{
REFM|FBrf0051969
|Xu and Artavanis-Tsakonas
|1990
REFM|FBrf0068437
|Busseau et al.
|1994
REFM|FBrf0141440
|Ramain et al.
|2001
REFM|FBrf0151854
|Duvic et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014443	ICL 1 Tirant	SYM 1 Tirant{}emc<up>D</up>	ASTR 1 -	CLOC 1 61C9	REF 1 3	DT 1 6 Jan 2000	RESZ 641
ID|FBti0014443
SYM|Tirant{}emc<up>D</up>
ASTP|<fbsym>FBtp0011467==Tirant</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Tirant
ASGN|<fbsym>FBgn0000575==emc</fbsym>
SK|FBst0001032
|emc[D] rho[ve-1] rs[2] st[1] bul[D]/TM1
|FBst0001189
|emc[D] st[1] in[1] kni[ri-1] p[p] Dr[Mio]/TM6C, ca[1]
|Total=2

REFDSR
{
RDID|FBrf0055956
|Cubas and Modolell
|1992
SYN|Tirant{}emc<up>D</up>
ASAL|<fbsym>FBal0003710==emc<up>D</up></fbsym>
MU|spontaneous
CLOC|61C9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000575==emc</fbsym>
}

REF
{
REFM|FBrf0055956
|Cubas and Modolell
|1992
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003710==emc<up>D</up></fbsym>

REFDSR
{
RDID|FBrf0051368
|Garrell and Modolell
|1990
PHP|Dominant.
}

REFDSR
{
RDID|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
PHP|Wings have plexi between LII and LIII on one side and between LIV and
|LV on the other. Terminal gaps of LV, thinner veins and broader than
|normal wings.
}

REFDSR
{
RDID|FBrf0055045
|Mari-Beffa et al.
|1991
PHP|Heterozygotes lack anterior-medial microchaetae.
| <fbsym>FBal0003710==emc<up>D</up></fbsym> reduces ASC
|transcription.
}

REFDSR
{
RDID|FBrf0063385
|Craymer
|1980
PHP|RK1
|Heterozygotes lack one or both postvertical bristles and often lack
|other bristles. Wing vein L5 is often incomplete. Homozygotes exhibit
|missing postvertical bristles and ocellars are absent or strongly reduced,
|patches of microchaetae and other bristles are often missing.
PHM|postvertical bristle
|ocellar bristle
|microchaeta
|macrochaeta
|wing vein L5
}

REFDSR
{
RDID|FBrf0074922
|de Celis et al.
|1991
PHP|Absence of specific macrochaetae on the notum and reduction of the
|total number of microchaetae. <fbsym>FBal0003710==emc<up>D</up></fbsym> corrects Hw
| phenotypes in both
|ectopic and normal positions.
}

REFDSR
{
RDID|FBrf0084540
|de Celis et al.
|1995
PHP|Mitotic clones in the wing tend to avoid veins.
}

REFDSR
{
RDID|FBrf0107601
|Baonza and Garcia-Bellido
|1999
PHP|Homozygotes have slightly smaller wings than normal and lack the distal
|region of wing vein L5.
PHM|wing vein L5
|wing
}

REF
{
REFM|FBrf0051368
|Garrell and Modolell
|1990
REFM|FBrf0052918
|Diaz-Benjumea and Garcia-Bellido
|1990
REFM|FBrf0055045
|Mari-Beffa et al.
|1991
REFM|FBrf0063385
|Craymer
|1980
REFM|FBrf0074922
|de Celis et al.
|1991
REFM|FBrf0084540
|de Celis et al.
|1995
REFM|FBrf0107601
|Baonza and Garcia-Bellido
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014447	ICL 1 blastopia	SYM 1 flea{}ey<up>R</up>	ASTR 1 -	CLOC 1 102C2	REF 1 6	DT 1 23 Aug 2003	RESZ 2010
ID|FBti0014447
SYM|flea{}ey<up>R</up>
SYN|blastopia{}ey<up>R</up>
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|23 Aug 2003
|6 Jan 2000
ICL|blastopia
ASGN|<fbsym>FBgn0005558==ey</fbsym>
SK|FBst0000639
|ci[1] <fbsym>FBal0003934==ey[R]</fbsym> sv[n]
|FBst0000641
|ci[1] gvl[1] <fbsym>FBal0003934==ey[R]</fbsym> sv[n]
|FBst0000651
|gvl[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0000683
|bw[1]; e[4]; ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0000705
|C(1;Y)1, In(1)dl-49, y[1]; bw[1]; e[4]; ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0000720
|C(4)RM-P2, ci[1] ey[R]: gvl[1] sv[n]
|FBst0001611
|y[1] pn[1]; C(4)RM, ci[1] ey[R]/0
|FBst0001612
|C(1)RM, y[1] v[1] bb[1]/0; C(4)RM, ci[1] ey[R]/0 & C(1;Y)1, v[1] f[1] B[1]/0; C(4)RM, ci[1] ey[R]/0
|FBst0001785
|C(4)RM, ci[1] ey[R]/0
|FBst0004059
|Dp(1;1)Co, y[2] w[a]/Ts(1Lt;4Lt)w[m5]; Ts(1Rt;4Rt)w[258-21]/ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0004228
|bt[1] <fbsym>FBal0003934==ey[R]</fbsym> sv[n]
|FBst0004229
|ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0004232
|gvl[1] <fbsym>FBal0003934==ey[R]</fbsym> sv[n]
|FBst0004258
|C(1;Y)1, y[1]/0; bw[1]; e[4]; ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0004260
|C(1)DX, y[1] f[1]; bw[1]; e[4]; ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0004361
|y[1]; bw[1]; e[4]; ci[1] <fbsym>FBal0003934==ey[R]</fbsym>
|FBst0004406
|y[1]; ry[506]; C(4)RM, ci[1] ey[R]/0
|FBst1001732
|0/C(1;Y), y[2] su(w[a]) w[a];  ci[1] <fbsym>FBal0003934==ey[R]</fbsym> sv[spa-pol]
|Total=18

REFDSR
{
RDID|FBrf0074219
|Quiring et al.
|1994
SYN|blastopia{}ey<up>R</up>
ASAL|<fbsym>FBal0003934==ey<up>R</up></fbsym>
MU|spontaneous
CLOC|102C2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005558==ey</fbsym>
}

REFDSR
{
RDID|FBrf0132376
|Callaerts et al.
|2001
PHC|lethal | partially | recessive
}

REF
{
REFM|FBrf0074219
|Quiring et al.
|1994
REFM|FBrf0081543
|Callaerts et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0106625
|Hauck et al.
|1999
REFM|FBrf0107506
|Xu et al.
|1999
REFM|FBrf0132376
|Callaerts et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0003934==ey<up>R</up></fbsym>

REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHP|Adult eyes vary in size from full to nothing, eye disc varies from
|rudimentary to full-sized.
PHM|eye
|eye-antennal disc
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye size relative to that of wild type: .25-.50
PHM|eye
}

REFDSR
{
RDID|FBrf0126718
|Kurata et al.
|2000
PHM|eye
}

REFDSR
{
RDID|FBrf0128595
|Noveen et al.
|2000
PHP|The medial lobe of the mushroom body is malformed, fused, missing or
|reduced in diameter in 38% of second instar larvae. The number of
|Kenyon cells is reduced. The diameter of the MB peduncle is not reduced.
|Embryonic pattern of mushroom body neuroblasts is apparently normal.
PHM|mushroom body
|medial branch of mushroom body
|Kenyon cell
}

REFDSR
{
RDID|FBrf0132376
|Callaerts et al.
|2001
PHP|Homozygotes show 30% lethality.
|Eyes are reduced in size in homozygotes; 5% have eyes that are 0-25%
|of wild-type size, 19% have eyes that are 25-50% of wild-type size,
|49% have eyes that are 50-75% of wild-type size and 27% have eyes that
|are 75-100% of wild-type size.
|Homozygotes have no overt defects in the mushroom body or central complex.
|97% of <fbsym>FBal0003934==ey<up>R</up></fbsym>/<fbsym>FBal0117526==ey<up>JD</up></fbsym> flies have
| eyes which are 75-100% of wild-type
|... (see <fbsym>FBal0003934==ey<up>R</up></fbsym> report)
PHM|eye
|(with ey<up>D1Da</up>) eye
|(with ey<up>JD</up>) eye
}

REFDSR
{
RDID|FBrf0144814
|Kronhamn et al.
|2002
PHP|<fbsym>FBal0003934==ey<up>R</up></fbsym>/<fbsym>FBal0028184==ey<up>D</up></fbsym> animals have small eyes.
PHM|(with ey<up>D</up>) eye
}

REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126718
|Kurata et al.
|2000
REFM|FBrf0128595
|Noveen et al.
|2000
REFM|FBrf0132376
|Callaerts et al.
|2001
REFM|FBrf0144814
|Kronhamn et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014454	ICL 1 gypsy	SYM 1 gypsy{}f<up>K</up>	ASTR 1 -	CLOC 1 15F4--7	REF 1 3	DT 1 6 Jan 2000	RESZ 483
ID|FBti0014454
SYM|gypsy{}f<up>K</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0000630==f</fbsym>

REFDSR
{
RDID|FBrf0056247
|Hoover et al.
|1992
SYN|gypsy{}f<up>K</up>
ASAL|<fbsym>FBal0003970==f<up>K</up></fbsym>
MU|spontaneous
CLOC|15F4--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000630==f</fbsym>
}

REF
{
REFM|FBrf0056247
|Hoover et al.
|1992
REFM|FBrf0064511
|Hoover et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003970==f<up>K</up></fbsym>

REFDSR
{
RDID|FBrf0064511
|Hoover et al.
|1993
PHP|Mild <fbsym>FBgn0000630==f</fbsym> bristle phenotype. Bristle phenotype is under the control
|of a second site modifier.
PHM|macrochaeta
|microchaeta
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|suppressed by <fbsym>FBal0016319==su(Hw)<up>2</up></fbsym>
}

REF
{
REFM|FBrf0064511
|Hoover et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014455	ICL 1 gypsy	SYM 1 gypsy{}f<up>X</up>	ASTR 1 -	CLOC 1 15F4--7	REF 1 2	DT 1 6 Jan 2000	RESZ 648
ID|FBti0014455
SYM|gypsy{}f<up>X</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0000630==f</fbsym>
SK|FBst0004073
|Tp(1;1)f[+ih], y[1] v[1] f[X]; T(2;3)bw[VA], bw[VA]/L[2] l(2)*[*]
|FBst0005670
|In(1)dl-49, y[1] w[1] M(1)15DEF[1:4C]/In(1)sc[8], lz[1] <fbsym>FBal0003975==f[X]</fbsym> B[1]
|Total=2

REFDSR
{
RDID|FBrf0065437
|Ishimaru and Saigo
|1993
SYN|gypsy{}f<up>X</up>
ASAL|<fbsym>FBal0003975==f<up>X</up></fbsym>
MU|X ray
CLOC|15F4--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000630==f</fbsym>
}

REF
{
REFM|FBrf0065437
|Ishimaru and Saigo
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003975==f<up>X</up></fbsym>

REFDSR
{
RDID|FBrf0006515
|Muller
|1946
PHP|"f<up>m</up>" flies (<fbsym>FBal0003975==f<up>X</up></fbsym>
| <fbsym>FBab0021550==Tp(1;1)f<up>+ih</up></fbsym> double mutant) show a variable
|phenotype; many have an ordinary <fbsym>FBgn0000630==f</fbsym> mutant phenotype, but a high percentage
|show coherent patches of the body, often of considerable size, in which
|the bristles are normal. Occasionally, almost the whole fly appears
|wild type.
PHM|macrochaeta
}

REFDSR
{
RDID|FBrf0098231
|Dickinson and Thatcher
|1997
PHP|Larvae exhibit an intermediate bristle phenotype within the denticles
|of all rows.
PHM|denticle belt
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|moderate - both macrochaetae and microchaetae clearly affected
|A medium f. Suppressed by su(f).
|hypomorph (Oster, Erlich, and Muller, 1958).
|RK1.
|suppressed by su(f)
|RK1
}

REF
{
REFM|FBrf0006515
|Muller
|1946
REFM|FBrf0098231
|Dickinson and Thatcher
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014456	ICL 1 Stalker	SYM 1 Stalker{}f<up>eu</up>	ASTR 1 -	CLOC 1 15F4--7	REF 1 2	DT 1 6 Jan 2000	RESZ 445
ID|FBti0014456
SYM|Stalker{}f<up>eu</up>
ASTP|<fbsym>FBtp0011465==Stalker</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Stalker
ASGN|<fbsym>FBgn0000630==f</fbsym>

REFDSR
{
RDID|FBrf0051630
|Georgiev et al.
|1990
SYN|Stalker{}f<up>eu</up>
ASAL|<fbsym>FBal0031238==f<up>eu</up></fbsym>
CLOC|15F4--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000630==f</fbsym>
}

REF
{
REFM|FBrf0051630
|Georgiev et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014457	ICL 1 P	SYM 1 P{}f<up>hd</up>	ASTR 1 -	CLOC 1 15F4--7	REF 1 5	DT 1 6 Jan 2000	RESZ 538
ID|FBti0014457
SYM|P{}f<up>hd</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000630==f</fbsym>

REFDSR
{
RDID|FBrf0064511
|Hoover et al.
|1993
SYN|P{}f<up>hd</up>
ASAL|<fbsym>FBal0034602==f<up>hd</up></fbsym>
CLOC|15F4--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000630==f</fbsym>
}

REF
{
REFM|FBrf0064511
|Hoover et al.
|1993
REFM|FBrf0083249
|Lankenau
|1995
REFM|FBrf0085417
|Lankenau et al.
|1996
REFM|FBrf0088371
|Lankenau et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0034602==f<up>hd</up></fbsym>

REFDSR
{
RDID|FBrf0064511
|Hoover et al.
|1993
PHP|Extreme <fbsym>FBgn0000630==f</fbsym> phenotype affecting the macrochaetae, microchaetae and
|trichomes.
PHM|macrochaeta
|microchaeta
|prothoracic dorsal trichome
|mesothoracic dorsal trichome
|metathoracic dorsal trichome
}

REFDSR
{
RDID|FBrf0083249
|Lankenau
|1995
PHP|<fbsym>FBtp0007303==P{falter}</fbsym> is able to revert the bristle phenotype.
PHM|macrochaeta
}

REFDSR
{
RDID|FBrf0128123
|Lankenau et al.
|2000
PHP|About of quarter of <fbsym>FBal0105029==f<up>asH</up></fbsym>/<fbsym>FBal0034602==f<up>hd</up></fbsym>
| flies possess at least one kinked
|bristle.
PHM|macrochaeta
}

REF
{
REFM|FBrf0064511
|Hoover et al.
|1993
REFM|FBrf0083249
|Lankenau
|1995
REFM|FBrf0128123
|Lankenau et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014481	ICL 1 P	SYM 1 P{}hop<up>air</up>	ASTR 1 -	CLOC 1 10B5--6	REF 1 4	DT 1 6 Jan 2000	RESZ 643
ID|FBti0014481
SYM|P{}hop<up>air</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0004864==hop</fbsym>

REFDSR
{
RDID|FBrf0053739
|Watson et al.
|1991
SYN|P{}hop<up>air</up>
ASAL|<fbsym>FBal0031501==hop<up>air</up></fbsym>
CLOC|10B5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004864==hop</fbsym>
PHC|lethal | larval stage | recessive
}

REFDSR
{
RDID|FBrf0064770
|Zinyk et al.
|1993
PHC|lethal | polyphasic | recessive
}

REF
{
REFM|FBrf0053739
|Watson et al.
|1991
REFM|FBrf0059077
|Hanratty and Dearolf
|1993
REFM|FBrf0064770
|Zinyk et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0031501==hop<up>air</up></fbsym>

REFDSR
{
RDID|FBrf0053739
|Watson et al.
|1991
PHP|Melanotic tumor formation and lethality are due to the same mutation.
|Mutations exhibit incomplete penetrance and expressivity of the melanotic
|tumor phenotype. Small and/or abnormally shaped brain. No visible
|lymph gland defects.
}

REFDSR
{
RDID|FBrf0059077
|Hanratty and Dearolf
|1993
PHP|Melanotic phenotype: encapsulation of abnormal cells or tissues by
|otherwise normal haemocytes.
}

REFDSR
{
RDID|FBrf0064770
|Zinyk et al.
|1993
PHP|Autoimmune mutation causing polyphasic lethality with melanotic tumor
|formation (Watson Dev. Genet. 12:173). This developmental arrest is
|slightly suppressed by <fbsym>FBal0000811==awd<up>K</up></fbsym>, in that average lethal
| phase shifted
|later.
}

REF
{
REFM|FBrf0053739
|Watson et al.
|1991
REFM|FBrf0059077
|Hanratty and Dearolf
|1993
REFM|FBrf0064770
|Zinyk et al.
|1993
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014518	ICL 1 ?	SYM 1 ?{}SamDC<up>c</up>	ASTR 1 -	CLOC 1 31D9	REF 1 3	DT 1 6 Jan 2000	RESZ 556
ID|FBti0014518
SYM|?{}SamDC<up>c</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0019932==SamDC</fbsym>
ARGS|FBgn0019932

REFDSR
{
RDID|FBrf0058585
|Clegg et al.
|1993
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
SYN|?{}SamDC<up>c</up>
ASAL|<fbsym>FBal0034916==SamDC<up>c</up></fbsym>
CLOC|31D9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0019932==SamDC</fbsym>
}

REF
{
REFM|FBrf0058585
|Clegg et al.
|1993
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0034916==SamDC<up>c</up></fbsym>

REFDSR
{
RDID|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
PHP|Eclosion is delayed by 3 days in homozygous flies, and the adults have
|a Minute-like bristle phenotype.
|<fbsym>FBal0034916==SamDC<up>c</up></fbsym> is lethal in combination with
| <fbsym>FBal0034918==SamDC<up>e</up></fbsym>, if <fbsym>FBal0034918==SamDC<up>e</up></fbsym>
|is maternally inherited.
| <fbsym>FBal0034916==SamDC<up>c</up></fbsym>/<fbsym>FBal0034918==SamDC<up>e</up></fbsym> flies in
| which <fbsym>FBal0034918==SamDC<up>e</up></fbsym>
|is paternally inherited show a 3 day delay in eclosion and the adults
|have a Minute-like bristle phenotype.
|Homozygous, heterozygous,
| <fbsym>FBal0034916==SamDC<up>c</up></fbsym>/<fbsym>FBal0034917==SamDC<up>d</up></fbsym>, <fbsym>FBal0034916==SamDC<up>c</up></fbsym>/<fbsym>FBal0034918==SamDC<up>e</up></fbsym>
|... (see <fbsym>FBal0034916==SamDC<up>c</up></fbsym> report)
PHM|macrochaeta
}

REF
{
REFM|FBrf0099842
|Larsson and Rasmuson-Lestander
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014537	ICL 1 ?	SYM 1 ?{}lz<up>K</up>	ASTR 1 -	CLOC 1 8D5--6	REF 1 2	DT 1 6 Jan 2000	RESZ 464
ID|FBti0014537
SYM|?{}lz<up>K</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0002576==lz</fbsym>
SK|FBst0002387
|lz[K]
|FBst0003657
|In(1)sc[260-14] lz[K]/C(1)DX, y[1] f[1]
|Total=2

REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
SYN|?{}lz<up>K</up>
ASAL|<fbsym>FBal0011825==lz<up>K</up></fbsym>
CLOC|8D5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002576==lz</fbsym>
}

REF
{
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0011825==lz<up>K</up></fbsym>

REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHP|A weak lz allele. Adult eye slightly rough, irregular facets shapes,
|eye disc appears normal.
}

REFDSR
{
RDID|FBrf0063599
|Krivshenko
|1956
PHP|Homozygous males have slightly narrow eyes, with uneven fused facets.
|Males are viable and fertile, homozygous females have not been obtained.
|Heterozygous females are phenotypically normal.
PHM|eye
|ommatidium
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|RK1.
|Tarsal claws normal. Spermathecae and parovaria present.
}

REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. The
|number of large and small basiconic sensilla is reduced. The density
|of the coeloconic sensilla on the antennal funiculus is increased and
|the density of the large basiconic sensilla on the antennal funiculus
|is decreased compared to wild-type.
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
}

REFDSR
{
RDID|FBrf0086985
|Daga et al.
|1996
PHP|Some ommatidia have a supernumerary R7 photoreceptor cell, and some
|have extra outer photoreceptor cells.
PHM|photoreceptor cell
}

REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygous females have normal eyes. Hemizygous males have a mild
|rough eye phenotype, with disruption of the ommatidial array at the
|posterior rim of the eye. Black pock marks are visible on the surface
|of the eye.
PHM|eye | posterior
|ommatidium
|eye
}

REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|Mild eye phenotype. Defects in photoreceptor neuron recruitment.
|Some facets have seven cells with larger, R1 to R6 like rhabdomeres,
|an R7-like cell is absent. Facets may have a duplicated R7 cells.
|Other facets have normal looking R7 cells but incorrect numbers of
|outer photoreceptor cells.
PHM|photoreceptor cell R1
|photoreceptor cell R2
|photoreceptor cell R3
|photoreceptor cell R4
|photoreceptor cell R5
|photoreceptor cell R6
|photoreceptor cell R7
}

REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|<fbsym>FBal0011825==lz<up>K</up></fbsym> adults have a mild mutant eye phenotype. Ectopic
| cell death
|is seen in third larval instar eye discs.
PHM|eye
|eye disc
}

REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0063599
|Krivshenko
|1956
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0086985
|Daga et al.
|1996
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014553	ICL 1 gypsy	SYM 1 gypsy{}br<up>npr-fs</up>	ASTR 1 -	CLOC 1 2B3--5	REF 1 2	DT 1 6 Jan 2000	RESZ 578
ID|FBti0014553
SYM|gypsy{}br<up>npr-fs</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0000210==br</fbsym>

REFDSR
{
RDID|FBrf0055826
|Huang and Orr
|1992
SYN|gypsy{}br<up>npr-fs</up>
ASAL|<fbsym>FBal0013162==br<up>npr-fs</up></fbsym>
MU|P-element activity
CLOC|2B3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000210==br</fbsym>
PHC|female sterile | recessive
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHC|female sterile | recessive
}

REF
{
REFM|FBrf0055826
|Huang and Orr
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0013162==br<up>npr-fs</up></fbsym>

REFDSR
{
RDID|FBrf0049940
|Orr et al.
|1989
PHP|Mature follicles of homozygous females have minor defects in the endochorion
|(which are uniformly distributed) and have defective respiratory appendages.
PHM|endochorion
|dorsal appendage
}

REFDSR
{
RDID|FBrf0055826
|Huang and Orr
|1992
PHP|In stage 13 of oogenesis nurse cell domain distension fails and subsequent
|readsorption of nurse cells produces a typical appendageless egg. Chorion
|gene amplification is abnormally arrested in stage 13 and 14 <fbsym>FBal0013162==br<up>npr-fs</up></fbsym>
|follicles. Mosaic experiments reveal a somatic but not germ line requirement
|for 'npr' function.
PHM|dorsal appendage
}

REFDSR
{
RDID|FBrf0099732
|Deng and Bownes
|1997
PHP|Females produce 'appendageless' eggs.
PHM|dorsal appendage
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Morphologically abnormal eggs that fail to hatch.
|Various defects in respiratory appendages and chorionic architecture.
PHM|chorion
|dorsal appendage
}

REF
{
REFM|FBrf0049940
|Orr et al.
|1989
REFM|FBrf0055826
|Huang and Orr
|1992
REFM|FBrf0099732
|Deng and Bownes
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014595	ICL 1 P	SYM 1 P{}r<up>hdt</up>	ASTR 1 -	CLOC 1 14F5--15A1	REF 1 2	DT 1 6 Jan 2000	RESZ 463
ID|FBti0014595
SYM|P{}r<up>hdt</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003189==r</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}r<up>hdt</up>
ASAL|<fbsym>FBal0014252==r<up>hdt</up></fbsym>
MU|PM hybrid dysgenesis
CLOC|14F5--15A1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003189==r</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014620	ICL 1 Doc	SYM 1 Doc{}sas<up>Doc</up>	ASTR 1 -	CLOC 1 84C8--D1	REF 1 2	DT 1 6 Jan 2000	RESZ 460
ID|FBti0014620
SYM|Doc{}sas<up>Doc</up>
ASTP|<fbsym>FBtp0011424==Doc</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Doc
ASGN|<fbsym>FBgn0002306==sas</fbsym>
ARGS|FBgn0002306

REFDSR
{
RDID|FBrf0073744
|Lim and Simmons
|1994
SYN|Doc{}sas<up>Doc</up>
ASAL|<fbsym>FBal0032641==sas<up>Doc</up></fbsym>
CLOC|84C8--D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002306==sas</fbsym>
}

REF
{
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014622	ICL 1 ?	SYM 1 ?{}sc<up>Ac</up>	ASTR 1 -	CLOC 1 1A8	REF 1 3	DT 1 6 Jan 2000	RESZ 431
ID|FBti0014622
SYM|?{}sc<up>Ac</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0004170==sc</fbsym>

REFDSR
{
RDID|FBrf0042024
|Campuzano et al.
|1985
SYN|?{}sc<up>Ac</up>
ASAL|<fbsym>FBal0015226==sc<up>Ac</up></fbsym>
CLOC|1A8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004170==sc</fbsym>
}

REF
{
REFM|FBrf0042024
|Campuzano et al.
|1985
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014631	ICL 1 P	SYM 1 P{}sli<up>P</up>	ASTR 1 -	CLOC 1 52C9--D1	REF 1 2	DT 1 6 Jan 2000	RESZ 463
ID|FBti0014631
SYM|P{}sli<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003425==sli</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}sli<up>P</up>
ASAL|<fbsym>FBal0015701==sli<up>P</up></fbsym>
MU|P-element activity
CLOC|52C9--D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003425==sli</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014632	ICL 1 P	SYM 1 P{}sn<up>(+)</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 2	DT 1 6 Jan 2000	RESZ 430
ID|FBti0014632
SYM|P{}sn<up>(+)</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
SYN|P{}sn<up>(+)</up>
ASAL|<fbsym>FBal0015769==sn<up>(+)</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0015769==sn<up>(+)</up></fbsym>

REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
PHP|Wild-type bristle phenotype.
}

REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014662	ICL 1 P	SYM 1 P{}sn<up>cm</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 2	DT 1 6 Jan 2000	RESZ 437
ID|FBti0014662
SYM|P{}sn<up>cm</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}sn<up>cm</up>
ASAL|<fbsym>FBal0015854==sn<up>cm</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0015854==sn<up>cm</up></fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|An allele of <fbsym>FBgn0003447==sn</fbsym> that is mutable in dysgenic but not in
|non-dysgenic genotypes. Mutation takes place in two directions; one is
|to apparent stable reversions and the other to a more extreme
|phenotype, <fbsym>FBal0015856==sn<up>ext</up></fbsym>, which is in turn unstable. Gnarled macrochaetae
|and kinky microchaetae.
PHM|macrochaeta
|microchaeta
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014663	ICL 1 P	SYM 1 P{}sn<up>e</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 3	DT 1 6 Jan 2000	RESZ 465
ID|FBti0014663
SYM|P{}sn<up>e</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
SYN|P{}sn<up>e</up>
ASAL|<fbsym>FBal0015855==sn<up>e</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014664	ICL 1 P	SYM 1 P{}sn<up>ext</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 2	DT 1 6 Jan 2000	RESZ 464
ID|FBti0014664
SYM|P{}sn<up>ext</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|P{}sn<up>ext</up>
ASAL|<fbsym>FBal0015856==sn<up>ext</up></fbsym>
MU|PM hybrid dysgenesis
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014687	ICL 1 jockey	SYM 1 jockey{}st<up>sp</up>	ASTR 1 -	CLOC 1 73A3	REF 1 2	DT 1 6 Jan 2000	RESZ 490
ID|FBti0014687
SYM|jockey{}st<up>sp</up>
ASTP|<fbsym>FBtp0011444==jockey</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|jockey
ASGN|<fbsym>FBgn0003515==st</fbsym>
SK|FBst0000612
|st[sp]
|Total=1

REFDSR
{
RDID|FBrf0086235
|ten Have et al.
|1995
SYN|jockey{}st<up>sp</up>
ASAL|<fbsym>FBal0016158==st<up>sp</up></fbsym>
MU|spontaneous
CLOC|73A3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003515==st</fbsym>
}

REF
{
REFM|FBrf0086235
|ten Have et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016158==st<up>sp</up></fbsym>

REFDSR
{
RDID|FBrf0005752
|Brehme and Demerec
|1942
PHP|Malpighian tubule color: pale yellow; distinguishable from wild-type.
}

REFDSR
{
RDID|FBrf0049915
|Tearle et al.
|1989
PHP|Spotted phenotype.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: scarlet with facets and groups of facets that appear wild
|type; darkening spreads in old fly.
|<fbsym>FBal0016158==st<up>sp</up></fbsym>/<fbsym>FBal0016127==st<up>1</up></fbsym> like <fbsym>FBal0016158==st<up>sp</up></fbsym>.
|RK2.
PHM|pigment cell
}

REF
{
REFM|FBrf0005752
|Brehme and Demerec
|1942
REFM|FBrf0049915
|Tearle et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014720	ICL 1 Tirant	SYM 1 Tirant{}sv<up>de</up>	ASTR 1 -	CLOC 1 102D4	REF 1 3	DT 1 6 Jan 2000	RESZ 674
ID|FBti0014720
SYM|Tirant{}sv<up>de</up>
ASTP|<fbsym>FBtp0011467==Tirant</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Tirant
ASGN|<fbsym>FBgn0005561==sv</fbsym>
SK|FBst0000662
|sv[de]/Dp(2;4)ey[D], Alp[eyD]: ey[D]
|FBst1001546
|f[36a]; sv[de]/ci[D]
|FBst1001659
|mwh h; ey[D]/sv[de]
|Total=3

REFDSR
{
RDID|FBrf0094793
|Goldschmidt
|1944
PHC|sterile
}

REFDSR
{
RDID|FBrf0103260
|Fu et al.
|1998
SYN|Tirant{}sv<up>de</up>
ASAL|<fbsym>FBal0016606==sv<up>de</up></fbsym>
MU|spontaneous
CLOC|102D4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005561==sv</fbsym>
}

REF
{
REFM|FBrf0094793
|Goldschmidt
|1944
REFM|FBrf0103260
|Fu et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016606==sv<up>de</up></fbsym>

REFDSR
{
RDID|FBrf0103260
|Fu et al.
|1998
PHP|<fbsym>FBal0092506==sv<up>spa-20</up></fbsym> strongly enhances the bristle phenotype of
| <fbsym>FBal0016606==sv<up>de</up></fbsym> in
|transheterozygotes; in the eyes there is nearly complete loss of bristle
|shafts, and in other parts of the body, loss or reduction of the shafts
|of microchaetae and macrochaetae is more severe than in
| <fbsym>FBal0016606==sv<up>de</up></fbsym> homozygotes.
PHM|microchaeta
|macrochaeta
|interommatidial bristle
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|More extreme than <fbsym>FBal0016607==sv<up>n</up></fbsym>. Thorax denuded over large
|areas. Phenotype more severe than <fbsym>FBal0005293==H<up>2</up></fbsym>; bristleless
|sockets found on adult integumentary derivatives of
|all imaginal discs; nearly 100% penetrance on thorax.
|Shafts, where present, often bent, twisted, or forked;
|up to 97% of bristle organs on wing costa and distal
|leg segments fail to produce normal shafts. Bracts
|... (see <fbsym>FBal0016606==sv<up>de</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0108432
|Kavaler et al.
|1999
PHP|<fbsym>FBal0016606==sv<up>de</up></fbsym>/<fbsym>FBab0002954==Df(4)G</fbsym> flies have more severe
| bristle defects than <fbsym>FBal0016606==sv<up>de</up></fbsym>
|homozygotes.
|Almost all homozygotes eclose, but the adults are uncoordinated and
|die within a few days of eclosion.
|Homozygotes show bristle defects over the entire body surface. The
|microchaetae and macrochaetae of the notum can have stunted or misshapen
|shafts, or may have empty sockets. Macrochaetae also occasionally
|... (see <fbsym>FBal0016606==sv<up>de</up></fbsym> report)
PHM|macrochaeta
|scutum & macrochaeta
|scutum & microchaeta
|scutum & macrochaeta & trichogen cell
|scutum & macrochaeta & tormogen cell
|anterior dorsocentral bristle & trichogen cell
|posterior dorsocentral bristle & tormogen cell
}

REF
{
REFM|FBrf0103260
|Fu et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108432
|Kavaler et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014721	ICL 1 blastopia	SYM 1 flea{}sv<up>n</up>	ASTR 1 -	CLOC 1 102D4	REF 1 2	DT 1 23 Aug 2003	RESZ 872
ID|FBti0014721
SYM|flea{}sv<up>n</up>
SYN|blastopia{}sv<up>n</up>
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|23 Aug 2003
|6 Jan 2000
ICL|blastopia
ASGN|<fbsym>FBgn0005561==sv</fbsym>
SK|FBst0000639
|ci[1] ey[R] <fbsym>FBal0016607==sv[n]</fbsym>
|FBst0000641
|ci[1] gvl[1] ey[R] <fbsym>FBal0016607==sv[n]</fbsym>
|FBst0000642
|ci[1] <fbsym>FBal0016607==sv[n]</fbsym>
|FBst0000663
|sv[n]
|FBst0000720
|C(4)RM-P2, ci[1] ey[R]: gvl[1] <fbsym>FBal0016607==sv[n]</fbsym>
|FBst0004228
|bt[1] ey[R] <fbsym>FBal0016607==sv[n]</fbsym>
|FBst0004232
|gvl[1] ey[R] <fbsym>FBal0016607==sv[n]</fbsym>
|Total=7

REFDSR
{
RDID|FBrf0103260
|Fu et al.
|1998
SYN|blastopia{}sv<up>n</up>
ASAL|<fbsym>FBal0016607==sv<up>n</up></fbsym>
CLOC|102D4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005561==sv</fbsym>
}

REF
{
REFM|FBrf0103260
|Fu et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0016607==sv<up>n</up></fbsym>

REFDSR
{
RDID|FBrf0103260
|Fu et al.
|1998
PHP|<fbsym>FBal0092506==sv<up>spa-20</up></fbsym> strongly enhances the bristle phenotype of
| <fbsym>FBal0016607==sv<up>n</up></fbsym> in
|transheterozygotes; in the eyes there is nearly complete loss of bristle
|shafts, and in other parts of the body, loss or reduction of the shafts
|of microchaetae and macrochaetae is more severe than in
| <fbsym>FBal0016607==sv<up>n</up></fbsym> homozygotes.
|The bristle phenotype of <fbsym>FBal0016607==sv<up>n</up></fbsym> mutants is entirely
| rescued on the
|notum, partially rescued in the eye and not rescued on the abdomen
|by <fbsym>FBal0092509==sv<up>2.0.cFa</up></fbsym>.
PHM|microchaeta
|macrochaeta
|interommatidial bristle
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Extremely short bristles. Viability excellent.
|Trichogen irregularly displaced, becoming more or less
|converted into tormogen (Lees and Waddington, 1943).
|Polarity of microchaetae in vicinity of double sockets
|disrupted such that they form a whorl around socket
|(Toney and Thompson, 1980). In triplo-4
| <fbsym>sv<up>n</up>&#64;/sv<up>n</up></fbsym>/<fbsym>FBal0016607==sv<up>n</up></fbsym>,
| the phenotype is more nearly normal than in diplo-4. ... (see
| <fbsym>FBal0016607==sv<up>n</up></fbsym> report) 
}

REFDSR
{
RDID|FBrf0108432
|Kavaler et al.
|1999
PHP|<fbsym>FBal0016607==sv<up>n</up></fbsym>/<fbsym>FBab0002954==Df(4)G</fbsym> flies have more severe
| bristle defects than <fbsym>FBal0016607==sv<up>n</up></fbsym>
|homozygotes.
|Homozygotes show bristle defects over the entire body surface. The
|microchaetae and macrochaetae of the notum often have stunted or misshapen
|shafts. Macrochaetae also occasionally show a double socket phenotype.
PHM|macrochaeta
|scutum & macrochaeta
|scutum & microchaeta
|scutum & microchaeta & trichogen cell
|scutum & macrochaeta & trichogen cell
}

REFDSR
{
RDID|FBrf0187662
|Sousa-Neves et al.
|2005
PHP|<fbsym>FBal0124929==sv<up>rugoso-nu</up></fbsym>/<fbsym>FBal0016607==sv<up>n</up></fbsym> flies show
| loss of hairs.
PHM|(with sv<up>rugoso-nu</up>) chaeta
}

REF
{
REFM|FBrf0103260
|Fu et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108432
|Kavaler et al.
|1999
REFM|FBrf0187662
|Sousa-Neves et al.
|2005
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014755	ICL 1 H	SYM 1 H{}vg<up>al</up>	ASTR 1 -	CLOC 1 49E1	REF 1 5	DT 1 6 Jan 2000	RESZ 540
ID|FBti0014755
SYM|H{}vg<up>al</up>
ASTP|<fbsym>FBtp0011431==hobo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|H
ASGN|<fbsym>FBgn0003975==vg</fbsym>

REFDSR
{
RDID|FBrf0054088
|Bazin et al.
|1991
SYN|H{}vg<up>al</up>
ASAL|<fbsym>FBal0035916==vg<up>al</up></fbsym>
CLOC|49E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003975==vg</fbsym>
}

REF
{
REFM|FBrf0054088
|Bazin et al.
|1991
REFM|FBrf0089591
|Bazin and Higuet
|1996
REFM|FBrf0098200
|Bonnivard et al.
|1997
REFM|FBrf0099521
|Silber et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035916==vg<up>al</up></fbsym>

REFDSR
{
RDID|FBrf0054088
|Bazin et al.
|1991
PHP|Wings have terminal notches and lateral excisions. Halteres and scutellar
|bristles are wild-type. Viability and fertility are normal.
PHM|wing
}

REFDSR
{
RDID|FBrf0099521
|Silber et al.
|1997
PHP|Wing length increases with increasing temperature.
PHM|wing | conditional cs
}

REF
{
REFM|FBrf0054088
|Bazin et al.
|1991
REFM|FBrf0099521
|Silber et al.
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014758	ICL 1 roo	SYM 1 roo{}vg<up>ni</up>	ASTR 1 -	CLOC 1 49E1	REF 1 2	DT 1 6 Jan 2000	RESZ 467
ID|FBti0014758
SYM|roo{}vg<up>ni</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0003975==vg</fbsym>
SK|FBst0000435
|vg[ni]
|Total=1

REFDSR
{
RDID|FBrf0047923
|Williams and Bell
|1988
SYN|roo{}vg<up>ni</up>
ASAL|<fbsym>FBal0017894==vg<up>ni</up></fbsym>
CLOC|49E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003975==vg</fbsym>
}

REF
{
REFM|FBrf0047923
|Williams and Bell
|1988
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0017894==vg<up>ni</up></fbsym>

REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|A change in phenotype, wing scalloping, was seen in tests for interaction
|with <fbsym>FBal0012671==mw<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0051947
|Rabinow and Birchler
|1990
PHP|Homozygotes are wild type, wing phenotype seen only when heterozygous
|with another <fbsym>FBgn0003975==vg</fbsym> allele.
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Homozygote normal; enhanced by Minutes; 1/4 of
| <fbsym>FBal0017894==vg<up>ni</up></fbsym>/<fbsym>FBal0017868==vg<up>1</up></fbsym> show
|wings nicks.
|RK3.
PHM|(with vg<up>1</up>) wing
}

REFDSR
{
RDID|FBrf0090702
|Morcillo et al.
|1996
PHP|<fbsym>FBal0002014==ct<up>L32</up></fbsym>; <fbsym>FBal0035732==su(Hw)<up>e2</up></fbsym> flies
| heterozygous for <fbsym>FBal0017894==vg<up>ni</up></fbsym> display a
|significant <fbsym>FBgn0004198==ct</fbsym> wing phenotype.
}

REF
{
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0051947
|Rabinow and Birchler
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0090702
|Morcillo et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014759	ICL 1 ?	SYM 1 ?{}vg<up>np</up>	ASTR 1 -	CLOC 1 49E1	REF 1 3	DT 1 6 Jan 2000	RESZ 526
ID|FBti0014759
SYM|?{}vg<up>np</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003975==vg</fbsym>
SK|FBst0000436
|vg[np]
|FBst1000796
|dl[4] pr vg[np]/ CyO, l(2)100[DTS]
|Total=2

REFDSR
{
RDID|FBrf0052606
|Williams et al.
|1990
SYN|?{}vg<up>np</up>
ASAL|<fbsym>FBal0017899==vg<up>np</up></fbsym>
MU|spontaneous
CLOC|49E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003975==vg</fbsym>
}

REF
{
REFM|FBrf0052606
|Williams et al.
|1990
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0017899==vg<up>np</up></fbsym>

REFDSR
{
RDID|FBrf0056344
|Bazin and Silber
|1992
PHP|Not suppressed by <fbsym>FBal0016572==Su(vg)B27<up>1</up></fbsym>,
| <fbsym>FBal0016573==Su(vg)E4<up>1</up></fbsym> or <fbsym>FBal0016574==Su(vg)E6<up>1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHP|Homozygotes display high resistance to aminopterin.
}

REFDSR
{
RDID|FBrf0090702
|Morcillo et al.
|1996
PHP|<fbsym>FBal0002014==ct<up>L32</up></fbsym>; <fbsym>FBal0035732==su(Hw)<up>e2</up></fbsym> flies
| heterozygous for <fbsym>FBal0017899==vg<up>np</up></fbsym> display a
|significant <fbsym>FBgn0004198==ct</fbsym> wing phenotype.
}

REFDSR
{
RDID|FBrf0099521
|Silber et al.
|1997
PHP|Wing length decreases with increasing temperature.
PHM|wing | conditional ts
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|terminal incisions in wings; overlaps wild type at 25<up>o</up>C, not at
| 19<up>o</up>C. Wing buds show scalloping.
|RK2.
}

REF
{
REFM|FBrf0056344
|Bazin and Silber
|1992
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0090702
|Morcillo et al.
|1996
REFM|FBrf0099521
|Silber et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014760	ICL 1 FB	SYM 1 FB{}w<up>+UR</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 6 Jan 2000	RESZ 553
ID|FBti0014760
SYM|FB{}w<up>+UR</up>
ASTP|<fbsym>FBtp0011426==FB</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|FB
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0006026
|Df(1)vt, sc[1] z[1] w[+UR]/FM6
|Total=1

REFDSR
{
RDID|FBrf0091149
|Rasmuson-Lestander and Ekstrom
|1996
SYN|FB{}w<up>+UR</up>
ASAL|<fbsym>FBal0033102==w<up>+UR</up></fbsym>
|<fbsym>FBal0033103==w<up>+UZ</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0091149
|Rasmuson-Lestander and Ekstrom
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0033103==w<up>+UZ</up></fbsym>

REFDSR
{
RDID|FBrf0055430
|Montell et al.
|1992
PHP|Eye color: yellow.
PHM|pigment cell
}

REF
{
REFM|FBrf0055430
|Montell et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014761	ICL 1 NOF	SYM 1 NOF{}w<up>+UZ</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 6 Jan 2000	RESZ 458
ID|FBti0014761
SYM|NOF{}w<up>+UZ</up>
ASTP|<fbsym>FBtp0011454==NOF</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|NOF
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0091149
|Rasmuson-Lestander and Ekstrom
|1996
SYN|NOF{}w<up>+UZ</up>
ASAL|<fbsym>FBal0033103==w<up>+UZ</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0091149
|Rasmuson-Lestander and Ekstrom
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0033103==w<up>+UZ</up></fbsym>

REFDSR
{
RDID|FBrf0055430
|Montell et al.
|1992
PHP|Eye color: yellow.
PHM|pigment cell
}

REF
{
REFM|FBrf0055430
|Montell et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014779	ICL 1 I	SYM 1 I{}w<up>IRI</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 6 Jan 2000	RESZ 426
ID|FBti0014779
SYM|I{}w<up>IRI</up>
ASTP|<fbsym>FBtp0011439==I-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|I
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0054158
|Rabinow et al.
|1991
SYN|I{}w<up>IRI</up>
ASAL|<fbsym>FBal0033140==w<up>IRI</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014781	ICL 1 Doc	SYM 1 Doc{}w<up>aG</up>	ASTR 1 -	CLOC 1 3B6	REF 1 3	DT 1 6 Jan 2000	RESZ 460
ID|FBti0014781
SYM|Doc{}w<up>aG</up>
ASTP|<fbsym>FBtp0011424==Doc</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Doc
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0068432
|Buff et al.
|1993
SYN|Doc{}w<up>aG</up>
ASAL|<fbsym>FBal0033144==w<up>aG</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0068432
|Buff et al.
|1993
REFM|FBrf0104490
|Nabirochkin et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014789	ICL 1 P	SYM 1 P{}w<up>apl</up>	ASTR 1 -	CLOC 1 3B6	REF 1 4	DT 1 6 Jan 2000	RESZ 575
ID|FBti0014789
SYM|P{}w<up>apl</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0054158
|Rabinow et al.
|1991
SYN|P{}w<up>apl</up>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
ASAL|<fbsym>FBal0018206==w<up>apl</up></fbsym>
MU|PM hybrid dysgenesis
}

REF
{
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0068460
|Csink et al.
|1994
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018206==w<up>apl</up></fbsym>

REFDSR
{
RDID|FBrf0084324
|Roseman et al.
|1995
PHP|Dosage compensation is almost equal in males and females in a <fbsym>FBal0032826==su(Hw)<up>V</up></fbsym>/<fbsym>FBal0016324==su(Hw)<up>7</up></fbsym>
|mutant background.
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REF
{
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0100562
|Frolov et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014791	ICL 1 blood	SYM 1 blood{}w<up>bl</up>	ASTR 1 -	CLOC 1 3B6	REF 1 8	DT 1 6 Jan 2000	RESZ 712
ID|FBti0014791
SYM|blood{}w<up>bl</up>
ASTP|<fbsym>FBtp0011415==blood</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|blood
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0004449
|w[bl]
|Total=1

REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
SYN|blood{}w<up>bl</up>
ASAL|<fbsym>FBal0018218==w<up>bl</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0098391
|Costas et al.
|1997
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018218==w<up>bl</up></fbsym>

REFDSR
{
RDID|FBrf0006364
|Ephrussi and Herold
|1945
PHP|Temperature sensitivity greatest 40-48 hr after pupation.
}

REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
PHP|Homozygous males are darker than homozygous females. Triple X metafemale
|individuals homozygous for <fbsym>FBal0018218==w<up>bl</up></fbsym> have pigment levels
| near the normal
|intensity of <fbsym>FBal0018218==w<up>bl</up></fbsym> homozygous XX females.
}

REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: yellowish-ruby, later <fbsym>FBgn0003351==se</fbsym>-like; female lighter than male;
|at 19<up>o</up>C as dark as <fbsym>FBal0013871==pn<up>1</up></fbsym>; at 30<up>o</up>C,
| as light as <fbsym>FBal0018215==w<up>bf</up></fbsym> or <fbsym>FBal0018254==w<up>i</up></fbsym>.
|Testis color: colorless.
|Malpighian tubule color: pale yellow at 25<up>o</up>C.
PHM|pigment cell
|testis pigment cell
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0105774
|Benevolenskaya et al.
|1998
PHM|pigment cell
}

REF
{
REFM|FBrf0006364
|Ephrussi and Herold
|1945
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105774
|Benevolenskaya et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014793	ICL 1 pogo	SYM 1 pogo{}w<up>ch</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 8 Jul 2003	RESZ 616
ID|FBti0014793
SYM|pogo{}w<up>ch</up>
SYN|Doc{pogo{}}w<up>ch</up>
|Doc{}w<up>1</up>
|pogo{}w<up>ch</up>
ASTP|<fbsym>FBtp0011457==pogo</fbsym>
DT|8 Jul 2003
|6 Jan 2000
ICL|pogo
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0004451
|w[ch] wy[1]/FM7c
|FBst0006250
|w[ch]; Su(w[ch])[1]/In(2L)Cy, In(2R)Cy, Cy[1] cn[2]
|Total=2

REFDSR
{
RDID|FBrf0087538
|Larsson et al.
|1996
SYN|pogo{}w<up>ch</up>
ASAL|<fbsym>FBal0018224==w<up>ch</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018224==w<up>ch</up></fbsym>

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: light yellow-pink.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0055430
|Montell et al.
|1992
PHP|Eye color: pinkish.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: translucent pink; male lighter than female.
|Eye color: light, with <fbsym>FBal0014434==rb<up>1</up></fbsym>.
|Eye color: light, with <fbsym>FBal0004957==g<up>1</up></fbsym>.
|Eye color: white, when heterozygous with <fbsym>FBal0018195==w<up>a</up></fbsym>.
|Ocellus color: pale.
|Testis color: colorless.
|Malpighian tubule color: colorless.
PHM|pigment cell
|Malpighian tubule
|testis pigment cell
|ocellus pigment granule
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have pink-orange eyes with only 2% red pigment (compared
|to 100% pigment in wild type).
PHM|pigment cell
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0055430
|Montell et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014794	ICL 1 coral	SYM 1 coral{}w<up>co</up>	ASTR 1 -	CLOC 1 3B6	REF 1 7	DT 1 6 Jan 2000	RESZ 676
ID|FBti0014794
SYM|coral{}w<up>co</up>
ASTP|<fbsym>FBtp0011421==coral</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|coral
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000153
|w[co] sn[2]
|Total=1

REFDSR
{
RDID|FBrf0068460
|Csink et al.
|1994
SYN|coral{}w<up>co</up>
ASAL|<fbsym>FBal0018225==w<up>co</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0068460
|Csink et al.
|1994
REFM|FBrf0074960
|Birchler et al.
|1994
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018225==w<up>co</up></fbsym>

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: deep ruby in male, darkening to <fbsym>FBgn0001087==g</fbsym>-like; lighter in female.
|Malpighian tubule color: pale yellow.
PHM|pigment cell
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have dull red eyes with 26% red pigment (compared to 100%
|pigment in wild type).
PHM|pigment cell
}

REF
{
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014795	ICL 1 pogo	SYM 1 pogo{}w<up>e</up>	ASTR 1 -	CLOC 1 3B6	REF 1 7	DT 1 8 Jul 2003	RESZ 1109
ID|FBti0014795
SYM|pogo{}w<up>e</up>
SYN|Doc{}w<up>1</up>
|pogo{}w<up>e</up>
ASTP|<fbsym>FBtp0011457==pogo</fbsym>
DT|8 Jul 2003
|6 Jan 2000
ICL|pogo
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000014
|br[1] <fbsym>FBal0018237==w[e]</fbsym> ec[1] rb[1] t[4]/FM1, lz[+]
|FBst0000159
|w[e]
|FBst0000269
|w[e]; cru[1] crs[1]
|FBst0000676
|w[e]; Dp(2;3)P, P[1], Gd[1]/TM6
|FBst0000737
|w[e] bb[l]/Y; l(2)mr[1]/In(2L)NS, In(2R)NS, l(2)35De[1] px[1] l(2)NS[1] sp[1]
|FBst0200525
|w[e]
|FBst0200537
|w[e]; pe[1]
|FBst0200538
|w[e]; st[1] pe[1]
|FBst0200542
|y[40a] w[e]; ap[1]
|Total=9

REFDSR
{
RDID|FBrf0054703
|O'Hare et al.
|1991
SYN|pogo{}w<up>e</up>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
ASAL|<fbsym>FBal0018237==w<up>e</up></fbsym>
MU|spontaneous
}

REF
{
REFM|FBrf0054703
|O'Hare et al.
|1991
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0057263
|Tudor et al.
|1992
REFM|FBrf0058549
|Sabl and Birchler
|1993
REFM|FBrf0084324
|Roseman et al.
|1995
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018237==w<up>e</up></fbsym>

REFDSR
{
RDID|FBrf0002371
|Muller
|1932
PHP|Amount of pigment formed by <fbsym>FBal0018237==w<up>e</up></fbsym> not a function of
| gene dose:
|<fbsym>FBal0018237==w<up>e</up></fbsym> female = <fbsym>FBal0018237==w<up>e</up></fbsym> male < <fbsym>FBal0018237==w<up>e</up></fbsym>/<fbsym>FBal0018237==w<up>e</up></fbsym>
|male = <fbsym>FBal0018237==w<up>e</up></fbsym>/<fbsym>FBal0018237==w<up>e</up></fbsym> female <
| <fbsym>FBal0018237==w<up>e</up></fbsym>/<fbsym>FBal0018237==w<up>e</up></fbsym>/<fbsym>FBal0018237==w<up>e</up></fbsym> female.
}

REFDSR
{
RDID|FBrf0003530
|Beadle and Ephrussi
|1936
PHP|A <fbsym>FBal0018237==w<up>e</up></fbsym> optic disk transplanted into a wild-type host
|shows autonomous eye color development.
}

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: light yellow-pink.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
PHP|Eye color: homozygous males lighter than homozygous females.
|Triple X metafemale individuals homozygous for <fbsym>FBal0018237==w<up>e</up></fbsym>
| have a darker
|eye color than <fbsym>FBal0018237==w<up>e</up></fbsym> homozygous XX females.
}

REFDSR
{
RDID|FBrf0086910
|Bhadra and Birchler
|1996
PHP|Decrease in wild type eye pigment in the presence of <fbsym>FBal0052163==Mow<up>gamma</up></fbsym>.
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: females, yellowish-pink; males lighter than females.
|Eye color: <fbsym>FBal0018237==w<up>e</up></fbsym>/<fbsym>FBal0018074==w<up>1</up></fbsym> females,
| similar to <fbsym>FBal0018237==w<up>e</up></fbsym> males.
|Testis color: colorless.
|Malpighian tubule color: colorless.
PHM|pigment cell
|Malpighian tubule
|testis pigment cell
}

REFDSR
{
RDID|FBrf0128132
|Benevolenskaya et al.
|2000
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have pink eyes with only 4% red pigment (compared to 100%
|pigment in wild type).
PHM|pigment cell
}

REF
{
REFM|FBrf0002371
|Muller
|1932
REFM|FBrf0003530
|Beadle and Ephrussi
|1936
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0056147
|Birchler
|1992
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128132
|Benevolenskaya et al.
|2000
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014798	ICL 1 roo	SYM 1 roo{}w<up>h</up>	ASTR 1 -	CLOC 1 3B6	REF 1 8	DT 1 8 Jul 2003	RESZ 789
ID|FBti0014798
SYM|roo{}w<up>h</up>
SYN|Doc{}w<up>1</up>
|roo{}w<up>h</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|8 Jul 2003
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000162
|w[h]
|Total=1

REFDSR
{
RDID|FBrf0054158
|Rabinow et al.
|1991
SYN|roo{}w<up>h</up>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
ASAL|<fbsym>FBal0018246==w<up>h</up></fbsym>
MU|spontaneous
}

REF
{
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0054703
|O'Hare et al.
|1991
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018246==w<up>h</up></fbsym>

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: light yellow.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0051869
|Rabinow and Birchler
|1990
PHP|Eye color: mottled with <fbsym>FBgn0002910==mw</fbsym>.
}

REFDSR
{
RDID|FBrf0063569
|Kaufman
|1969
PHP|Eye color: The <fbsym>FBal0018223==w<up>cf2</up></fbsym> eye color is not diluted when
| <fbsym>FBal0018223==w<up>cf2</up></fbsym> is
|in transheterozygous combination with <fbsym>FBal0018246==w<up>h</up></fbsym>.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0064501
|Heinrich et al.
|1993
PHP|Eye color: unaffected by <fbsym>FBal0063073==LTSV\RBZ<up>hs.w</up></fbsym>.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0100562
|Frolov et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: between <fbsym>FBal0018215==w<up>bf</up></fbsym> and
| <fbsym>FBal0018198==w<up>a4</up></fbsym>; slightly darker in male than in female.
|Malpighian tubule color: colorless.
PHM|pigment cell
|Malpighian tubule
}

REFDSR
{
RDID|FBrf0105774
|Benevolenskaya et al.
|1998
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0128132
|Benevolenskaya et al.
|2000
PHM|pigment cell
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0051869
|Rabinow and Birchler
|1990
REFM|FBrf0063569
|Kaufman
|1969
REFM|FBrf0064501
|Heinrich et al.
|1993
REFM|FBrf0100562
|Frolov et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105774
|Benevolenskaya et al.
|1998
REFM|FBrf0128132
|Benevolenskaya et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014803	ICL 1 F	SYM 1 F{}w<up>i+A</up>	ASTR 1 -	CLOC 1 3B6	REF 1 3	DT 1 6 Jan 2000	RESZ 477
ID|FBti0014803
SYM|F{}w<up>i+A</up>
ASTP|<fbsym>FBtp0011425==F-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|F
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0047228
|di Nocera and Casari
|1987
SYN|F{}w<up>i+A</up>
ASAL|<fbsym>FBal0018256==w<up>i+A</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0047228
|di Nocera and Casari
|1987
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018256==w<up>i+A</up></fbsym>

REFDSR
{
RDID|FBrf0037618
|Karess and Rubin
|1982
PHP|Eye color: wild-type.
}

REF
{
REFM|FBrf0037618
|Karess and Rubin
|1982
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014804	ICL 1 roo	SYM 1 roo{}w<up>is</up>	ASTR 1 -	CLOC 1 3B6	REF 1 3	DT 1 6 Jan 2000	RESZ 889
ID|FBti0014804
SYM|roo{}w<up>is</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0005572
|sc[1] z[1] w[is]; Su(z)2[1.b7]/CyO
|FBst0005573
|sc[1] z[1] w[is]; Su(z)2[1]/CyO
|FBst0006237
|sc[1] z[1] w[is]; M(2)21AB[1]/In(2L)Cy, In(2R)Cy, Cy[1] cn[2]
|FBst0006238
|sc[1] z[1] w[is]; Su(z)6[1]/In(2L)Cy, In(2R)Cy, Cy[1] cn[2]
|FBst0006239
|sc[1] z[1] w[is]; Su(z)7[1]/In(2L)Cy, In(2R)Cy, Cy[1] cn[2]
|FBst0006253
|sc[1] z[1] w[is]; Su(z)4[1]/TM3, Sb[1] Ser[1]
|Total=6

REFDSR
{
RDID|FBrf0068645
|Rasmuson-Lestander et al.
|1993
SYN|roo{}w<up>is</up>
ASAL|<fbsym>FBal0018267==w<up>is</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0068645
|Rasmuson-Lestander et al.
|1993
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018267==w<up>is</up></fbsym>

REFDSR
{
RDID|FBrf0068645
|Rasmuson-Lestander et al.
|1993
PHP|Eye color: orange, in <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018267==w<up>is</up></fbsym>/Y males.
|<fbsym>FBal0018822==z<up>1</up></fbsym> is dominant over <fbsym>FBgn0004050==z</fbsym><up>+</up> in the interaction
|with <fbsym>FBal0018267==w<up>is</up></fbsym>.
}

REFDSR
{
RDID|FBrf0082794
|Wu and Howe
|1995
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0094184
|Birve and Rasmuson-Lestander
|1994
PHP|Repression of <fbsym>FBal0018267==w<up>is</up></fbsym> by <fbsym>FBal0018822==z<up>1</up></fbsym> is
| suppressed by <fbsym>FBal0063038==Su(z)12<up>1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: wild-type.
|Male has greatly reduced amount of isoxanthopterin in abdomen.
|Eye color: variegated, <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018267==w<up>is</up></fbsym> male; between <fbsym>FBal0018822==z<up>1</up></fbsym> and wild-type.
}

REF
{
REFM|FBrf0068645
|Rasmuson-Lestander et al.
|1993
REFM|FBrf0082794
|Wu and Howe
|1995
REFM|FBrf0094184
|Birve and Rasmuson-Lestander
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014805	ICL 1 roo	SYM 1 copia{roo{}}w<up>ric</up>	ASTR 1 -	CLOC 1 3B6	REF 1 8	DT 1 29 Nov 2005	RESZ 874
ID|FBti0014805
SYM|copia{roo{}}w<up>ric</up>
SYN|roo{}w<up>ric</up>
ASTP|<fbsym>FBtp0019627==copia{roo{}}</fbsym>
DT|29 Nov 2005
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0073744
|Lim and Simmons
|1994
SYN|roo{}w<up>ric</up>
ASAL|<fbsym>FBal0018294==w<up>ric</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0152010
|Mukae et al.
|2002
CC|Nested insertion of <fbsym>FBgn0000155==roo</fbsym> element into <fbsym>FBgn0000349==copia</fbsym> element.
}

REF
{
REFM|FBrf0068460
|Csink et al.
|1994
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152010
|Mukae et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0018294==w<up>ric</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: like <fbsym>FBal0018195==w<up>a</up></fbsym>.
PHM|pigment cell
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014810	ICL 1 gypsy	SYM 1 gypsy{}y<up>+Ds</up>	ASTR 1 -	CLOC 1 1A5	REF 1 2	DT 1 6 Jan 2000	RESZ 440
ID|FBti0014810
SYM|gypsy{}y<up>+Ds</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0055739
|Kroczynska et al.
|1992
SYN|gypsy{}y<up>+Ds</up>
ASAL|<fbsym>FBal0033189==y<up>+Ds</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REF
{
REFM|FBrf0055739
|Kroczynska et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0033189==y<up>+Ds</up></fbsym>

REFDSR
{
RDID|FBrf0055739
|Kroczynska et al.
|1992
PHP|Body color: darker than wild-type in body and wing, with bristles unaffected.
}

REF
{
REFM|FBrf0055739
|Kroczynska et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014811	ICL 1 gypsy	SYM 1 gypsy{}y<up>+ms</up>	ASTR 1 -	CLOC 1 1A5	REF 1 2	DT 1 6 Jan 2000	RESZ 440
ID|FBti0014811
SYM|gypsy{}y<up>+ms</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0055739
|Kroczynska et al.
|1992
SYN|gypsy{}y<up>+ms</up>
ASAL|<fbsym>FBal0033194==y<up>+ms</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REF
{
REFM|FBrf0055739
|Kroczynska et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0033194==y<up>+ms</up></fbsym>

REFDSR
{
RDID|FBrf0055739
|Kroczynska et al.
|1992
PHP|Body color: bristles wild-type; body and wing slightly reduced <fbsym>FBgn0004034==y</fbsym><up>+</up> expression.
}

REF
{
REFM|FBrf0055739
|Kroczynska et al.
|1992
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014832	ICL 1 ?	SYM 1 ?{}y<up>td</up>	ASTR 1 -	CLOC 1 1A5	REF 1 2	DT 1 6 Jan 2000	RESZ 413
ID|FBti0014832
SYM|?{}y<up>td</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
SYN|?{}y<up>td</up>
ASAL|<fbsym>FBal0018729==y<up>td</up></fbsym>
MU|spontaneous
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018729==y<up>td</up></fbsym>

REFDSR
{
RDID|FBrf0044248
|Chia et al.
|1986
PHP|Body color: type 2 allele - some areas of cuticle are wild type, others
|have mutant pigmentation.
PHM|adult cuticle
}

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Body color: bristles, hairs, wild-type.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Body color: body rich tan, antennae light yellow, bristles black.
|Larval mouth part color: golden brown.
PHM|adult cuticle
|antenna
|cephalopharyngeal skeleton
}

REF
{
REFM|FBrf0044248
|Chia et al.
|1986
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014874	ICL 1 gypsy	SYM 1 gypsy{}pho<up>c</up>	ASTR 1 -	CLOC 1 102D6	REF 1 4	DT 1 6 Jan 2000	RESZ 726
ID|FBti0014874
SYM|gypsy{}pho<up>c</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0002521==pho</fbsym>

REFDSR
{
RDID|FBrf0044158
|Breen and Duncan
|1986
PHC|lethal | pharate adult stage
}

REFDSR
{
RDID|FBrf0068508
|Girton and Jeon
|1994
PHC|lethal | pharate adult stage | recessive
}

REFDSR
{
RDID|FBrf0102896
|Brown et al.
|1998
SYN|gypsy{}pho<up>c</up>
ASAL|<fbsym>FBal0039758==pho<up>c</up></fbsym>
MU|spontaneous
CLOC|102D6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002521==pho</fbsym>
PHC|lethal
}

REF
{
REFM|FBrf0044158
|Breen and Duncan
|1986
REFM|FBrf0068508
|Girton and Jeon
|1994
REFM|FBrf0102896
|Brown et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0039758==pho<up>c</up></fbsym>

REFDSR
{
RDID|FBrf0068508
|Girton and Jeon
|1994
PHP|Homozygotes, hemizygotes and heteroallelic with <fbsym>FBal0039758==pho<up>c</up></fbsym>
| die as pharate
|adults. Pupae exhibit transformation of antenna into legs, partial
|transformation of meso- and metathoracic legs into prothoracic, pattern
|duplications (presence of a sixth tarsal segment) and deficiencies
|in the legs (partial claw formation), partial transformation of abdominal
|segments to a more posterior identity and transformation of parovaria
|into spermathecia.
PHM|antenna & pupa
|mesothoracic leg & pupa
|metathoracic leg & pupa
|prothoracic tarsus & pupa
|mesothoracic tarsus & pupa
|metathoracic tarsus & pupa
|pupal abdomen
|female accessory gland & pupa
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|pupal lethal
}

REF
{
REFM|FBrf0068508
|Girton and Jeon
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014882	ICL 1 Dsim\ninja	SYM 1 Dsim\ninja{}Dsim\w<up>cho</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 6 Jan 2000	RESZ 459
ID|FBti0014882
SYM|Dsim\ninja{}Dsim\w<up>cho</up>
ASTP|<fbsym>FBtp0011473==Dsim\ninja</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Dsim\ninja
ASGN|<fbsym>FBgn0012902==Dsim\w</fbsym>

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|Dsim\ninja{}Dsim\w<up>cho</up>
ASAL|<fbsym>FBal0042521==Dsim\w<up>cho</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0012902==Dsim\w</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014903	ICL 1 P	SYM 1 P{}nos<up>BN</up>	ASTR 1 -	CLOC 1 91F4	REF 1 3	DT 1 6 Jan 2000	RESZ 481
ID|FBti0014903
SYM|P{}nos<up>BN</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0002962==nos</fbsym>

REFDSR
{
RDID|FBrf0087514
|Kobayashi et al.
|1996
SYN|P{}nos<up>BN</up>
ASAL|<fbsym>FBal0044220==nos<up>BN</up></fbsym>
CLOC|91F4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002962==nos</fbsym>
}

REF
{
REFM|FBrf0087514
|Kobayashi et al.
|1996
REFM|FBrf0101903
|Forbes and Lehmann
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0044220==nos<up>BN</up></fbsym>

REFDSR
{
RDID|FBrf0078260
|Curtis et al.
|1995
PHM|abdominal segment
}

REFDSR
{
RDID|FBrf0087514
|Kobayashi et al.
|1996
PHP|Pole cells fail to migrate into the gonads. Transplantation of pole
|cells into hosts that can form normal abdomens demonstrates the pole
|cells cannot penetrate the gonads. No <fbsym>FBal0013375==ovo<up>D1</up></fbsym> females transplanted
|with <fbsym>FBal0044220==nos<up>BN</up></fbsym> pole cells produce progeny, also
| demonstrating the pole
|cells cannot penetrate the gonads.
PHM|pole cell
}

REFDSR
{
RDID|FBrf0101903
|Forbes and Lehmann
|1998
PHP|The effects of loss of maternal and zygotic <fbsym>FBgn0002962==nos</fbsym> product on germ cell
|migration is studied in females with <fbsym>FBal0005406==hb<up>15</up></fbsym>
| <fbsym>FBal0044220==nos<up>BN</up></fbsym> mutant germ
|line clones crossed to
| <fbsym>FBal0013151==nos<up>18</up></fbsym>/<fbsym>FBab0002537==Df(3R)Dl-FX3</fbsym> males. Germ cells
|are formed in the embryos indicating <fbsym>FBgn0002962==nos</fbsym> function is not required
|for their formation. <fbsym>FBgn0002962==nos</fbsym> activity is essential for germ cell migration,
|from stage 10 onwards. Following exit of the germ cells of the posterior
|midgut pocket, germ cells fail to migrate over the surface of the gut
|... (see <fbsym>FBal0044220==nos<up>BN</up></fbsym> report)
}

REFDSR
{
RDID|FBrf0111783
|Asaoka-Taguchi et al.
|1999
PHP|The average number of pole cells per embryo is reduced compared to
|controls in embryos derived from homozygous females.
PHM|pole cell
}

REFDSR
{
RDID|FBrf0111849
|Deshpande et al.
|1999
PHP|Germ cells clump prematurely and stay in the middle of the embryo.
PHM|germ cell
}

REFDSR
{
RDID|FBrf0131417
|Verrotti and Wharton
|2000
PHM|embryonic abdominal segment
}

REFDSR
{
RDID|FBrf0148963
|Gamberi et al.
|2002
PHP|Homozygotes show severe head involution defects in only 4% of larvae.
PHM|dorsal closure stage embryo
}

REFDSR
{
RDID|FBrf0179243
|Hayashi et al.
|2004
PHP|Beginning at stage 9/10, most pole cells are lost in embryos derived
|from homozygous females. The pole cells in these embryos sometimes
|show irregular shapes characteristic of apoptotic cells and 19.7% are
|TUNEL-positive.
PHM|pole cell | maternal effect
}

REF
{
REFM|FBrf0078260
|Curtis et al.
|1995
REFM|FBrf0087514
|Kobayashi et al.
|1996
REFM|FBrf0101903
|Forbes and Lehmann
|1998
REFM|FBrf0111783
|Asaoka-Taguchi et al.
|1999
REFM|FBrf0111849
|Deshpande et al.
|1999
REFM|FBrf0131417
|Verrotti and Wharton
|2000
REFM|FBrf0148963
|Gamberi et al.
|2002
REFM|FBrf0179243
|Hayashi et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014909	ICL 1 Dvir\Penel	SYM 1 Dvir\Penelope{}Dvir\y<up>d</up>	ASTR 1 -	CLOC 1 1D	REF 1 2	DT 1 6 Jan 2000	RESZ 483
ID|FBti0014909
SYM|Dvir\Penelope{}Dvir\y<up>d</up>
ASTP|<fbsym>FBtp0011475==Dvir\Penelope</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Dvir\Penel
ASGN|<fbsym>FBgn0015690==Dvir\y</fbsym>

REFDSR
{
RDID|FBrf0091057
|Evgen'ev et al.
|1997
SYN|Dvir\Penelope{}Dvir\y<up>d</up>
ASAL|<fbsym>FBal0044761==Dvir\y<up>d</up></fbsym>
CLOC|1D
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0015690==Dvir\y</fbsym>
}

REF
{
REFM|FBrf0091057
|Evgen'ev et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014910	ICL 1 P	SYM 1 P{}amn<up>EX</up>	ASTR 1 -	CLOC 1 18F4--19A2	REF 1 2	DT 1 6 Jan 2000	RESZ 442
ID|FBti0014910
SYM|P{}amn<up>EX</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000076==amn</fbsym>

REFDSR
{
RDID|FBrf0081985
|Feany and Quinn
|1995
SYN|P{}amn<up>EX</up>
ASAL|<fbsym>FBal0045335==amn<up>EX</up></fbsym>
CLOC|18F4--19A2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000076==amn</fbsym>
}

REF
{
REFM|FBrf0081985
|Feany and Quinn
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0045335==amn<up>EX</up></fbsym>

REFDSR
{
RDID|FBrf0081985
|Feany and Quinn
|1995
PHP|Learning is wild type but memory is severely curtailed.
}

REF
{
REFM|FBrf0081985
|Feany and Quinn
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014929	ICL 1 H	SYM 1 H{}sca<up>MSKF</up>	ASTR 1 -	CLOC 1 49C3--D3	REF 1 2	DT 1 6 Jan 2000	RESZ 446
ID|FBti0014929
SYM|H{}sca<up>MSKF</up>
ASTP|<fbsym>FBtp0011431==hobo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|H
ASGN|<fbsym>FBgn0003326==sca</fbsym>
ARGS|FBgn0003326

REFDSR
{
RDID|FBrf0084048
|Hu et al.
|1995
SYN|H{}sca<up>MSKF</up>
ASAL|<fbsym>FBal0046410==sca<up>MSKF</up></fbsym>
CLOC|49C3--D3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003326==sca</fbsym>
}

REF
{
REFM|FBrf0084048
|Hu et al.
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0046410==sca<up>MSKF</up></fbsym>

REFDSR
{
RDID|FBrf0084048
|Hu et al.
|1995
PHP|Heterozygotes show occasional extra bristles. Homozygotes have rougher
|eyes and a larger number of bristles than homozygous <fbsym>FBgn0003326==sca</fbsym> null mutants.
PHM|eye
|macrochaeta
}

REFDSR
{
RDID|FBrf0104762
|Lee et al.
|1998
PHP|<fbsym>FBal0046410==sca<up>MSKF</up></fbsym>/<fbsym>FBal0032653==sca<up>BP2</up></fbsym> flies have
| extra thoracic bristles.
PHM|adult thorax & macrochaeta
}

REF
{
REFM|FBrf0084048
|Hu et al.
|1995
REFM|FBrf0104762
|Lee et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014969	ICL 1 P	SYM 1 P{}z<up>&pgr;r</up>	ASTR 1 -	CLOC 1 3A3	REF 1 2	DT 1 6 Jan 2000	RESZ 432
ID|FBti0014969
SYM|P{}z<up>&pgr;r</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0004050==z</fbsym>

REFDSR
{
RDID|FBrf0042424
|Mariani et al.
|1985
SYN|P{}z<up>pir</up>
ASAL|<fbsym>FBal0046871==z<up>&pgr;r</up></fbsym>
CLOC|3A3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004050==z</fbsym>
}

REF
{
REFM|FBrf0042424
|Mariani et al.
|1985
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014987	ICL 1 ?	SYM 1 ?{}Sxl<up>fb</up>	ASTR 1 -	CLOC 1 6F3--5	REF 1 2	DT 1 6 Jan 2000	RESZ 441
ID|FBti0014987
SYM|?{}Sxl<up>fb</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003659==Sxl</fbsym>

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
SYN|?{}Sxl<up>fb</up>
ASAL|<fbsym>FBal0049190==Sxl<up>fb</up></fbsym>
CLOC|6F3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003659==Sxl</fbsym>
PHC|lethal | recessive | female | partially
}

REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0049190==Sxl<up>fb</up></fbsym>

REFDSR
{
RDID|FBrf0054147
|Granadino et al.
|1991
PHP|Fully complements <fbsym>FBal0016689==Sxl<up>fLS</up></fbsym>. Homozygous females show a
| high degree
|of lethality; 70% die as embryos, 28% die as larvae. Those that survive
|are normal females. Homozygous clones also develop female structures.
|Homozygous germ cell clones give rise to functional eggs. <fbsym>FBal0016685==Sxl<up>f7,M1</up></fbsym>/<fbsym>FBal0049190==Sxl<up>fb</up></fbsym>
|flies lack gonads and occasionally have a male spot on the fifth and
|sixth tergites. Viability is greatly reduced in heterozygous combination
|with <fbsym>FBab0000599==Df(1)N71</fbsym> or <fbsym>FBab0000974==Df(1)svr</fbsym>.
}

REF
{
REFM|FBrf0054147
|Granadino et al.
|1991
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015007	ICL 1 ?	SYM 1 ?{}v<up>Amh</up>	ASTR 1 -	CLOC 1 9F11	REF 1 2	DT 1 6 Jan 2000	RESZ 382
ID|FBti0015007
SYM|?{}v<up>Amh</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003965==v</fbsym>

REFDSR
{
RDID|FBrf0056245
|Nivard et al.
|1992
SYN|?{}v<up>Amh</up>
ASAL|<fbsym>FBal0050730==v<up>Amh</up></fbsym>
CLOC|9F11
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003965==v</fbsym>
}

REF
{
REFM|FBrf0056245
|Nivard et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015012	ICL 1 P	SYM 1 P{}w<up>hd-R</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 6 Jan 2000	RESZ 453
ID|FBti0015012
SYM|P{}w<up>hd-R</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0064531
|Johnson-Schlitz and Engels
|1993
SYN|P{}w<up>hd-R</up>
ASAL|<fbsym>FBal0050891==w<up>hd-R</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0064531
|Johnson-Schlitz and Engels
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015019	ICL 1 P	SYM 1 P{}vn<up>wvn</up>	ASTR 1 -	CLOC 1 64E12--F2	REF 1 3	DT 1 6 Jan 2000	RESZ 474
ID|FBti0015019
SYM|P{}vn<up>wvn</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003984==vn</fbsym>

REFDSR
{
RDID|FBrf0089826
|Simcox et al.
|1996
SYN|P{}vn<up>wvn</up>
ASAL|<fbsym>FBal0050928==vn<up>wvn</up></fbsym>
CLOC|64E12--F2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003984==vn</fbsym>
}

REF
{
REFM|FBrf0089826
|Simcox et al.
|1996
REFM|FBrf0090788
|Schnepp et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0050928==vn<up>wvn</up></fbsym>

REFDSR
{
RDID|FBrf0089826
|Simcox et al.
|1996
PHP|Homozygotes exhibit interruption of wing vein 4 (usually in the central
|portion) and the anterior crossvein is absent.
PHM|wing vein L4
|anterior crossvein
}

REFDSR
{
RDID|FBrf0179189
|Donaldson et al.
|2004
PHP|Mutant flies show partial loss of wing vein L4.
PHM|wing vein L4
}

REF
{
REFM|FBrf0089826
|Simcox et al.
|1996
REFM|FBrf0179189
|Donaldson et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015035	ICL 1 Dsim\ninja	SYM 1 Dsim\ninja{}Dsim\w<up>mky</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 6 Jan 2000	RESZ 461
ID|FBti0015035
SYM|Dsim\ninja{}Dsim\w<up>mky</up>
ASTP|<fbsym>FBtp0011473==Dsim\ninja</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|Dsim\ninja
ASGN|<fbsym>FBgn0012902==Dsim\w</fbsym>

REFDSR
{
RDID|FBrf0098509
|Ogura and Yamamoto
|1995
SYN|Dsim\ninja{}Dsim\w<up>mky</up>
ASAL|<fbsym>FBal0053275==Dsim\w<up>mky</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0012902==Dsim\w</fbsym>
}

REF
{
REFM|FBrf0098509
|Ogura and Yamamoto
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0053275==Dsim\w<up>mky</up></fbsym>

REFDSR
{
RDID|FBrf0098117
|Coyne
|1997.1.2
PHP|Eye color: cream.
PHM|pigment cell
}

REF
{
REFM|FBrf0098117
|Coyne
|1997.1.2
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015051	ICL 1 roo	SYM 1 roo{}ct<up>P</up>	ASTR 1 -	CLOC 1 7B4--6	REF 1 2	DT 1 6 Jan 2000	RESZ 430
ID|FBti0015051
SYM|roo{}ct<up>P</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0004198==ct</fbsym>

REFDSR
{
RDID|FBrf0050015
|Georgiev et al.
|1989
SYN|roo{}ct<up>P</up>
ASAL|<fbsym>FBal0057676==ct<up>P</up></fbsym>
CLOC|7B4--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004198==ct</fbsym>
}

REF
{
REFM|FBrf0050015
|Georgiev et al.
|1989
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015057	ICL 1 ?	SYM 1 ?{}w<up>str</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 6 Jan 2000	RESZ 387
ID|FBti0015057
SYM|?{}w<up>str</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0090437
|Aslanukov et al.
|1996
SYN|?{}w<up>str</up>
ASAL|<fbsym>FBal0059694==w<up>str</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0090437
|Aslanukov et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0059694==w<up>str</up></fbsym>

REFDSR
{
RDID|FBrf0090437
|Aslanukov et al.
|1996
PHP|Eye color: uniform light.
PHM|pigment cell
}

REF
{
REFM|FBrf0090437
|Aslanukov et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015069	ICL 1 P	SYM 1 P{}esg<up>flg</up>	ASTR 1 -	CLOC 1 35D2	REF 1 2	DT 1 6 Jan 2000	RESZ 427
ID|FBti0015069
SYM|P{}esg<up>flg</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0001981==esg</fbsym>

REFDSR
{
RDID|FBrf0093866
|Roote
|1997.6.6
SYN|P{}esg<up>flg</up>
ASAL|<fbsym>FBal0061439==esg<up>flg</up></fbsym>
CLOC|35D2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001981==esg</fbsym>
}

REF
{
REFM|FBrf0093866
|Roote
|1997.6.6
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015071	ICL 1 jockey	SYM 1 jockey{}Adh<up>jockey</up>	ASTR 1 -	CLOC 1 35B3	REF 1 3	DT 1 6 Jan 2000	RESZ 509
ID|FBti0015071
SYM|jockey{}Adh<up>jockey</up>
ASTP|<fbsym>FBtp0011444==jockey</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|jockey
ASGN|<fbsym>FBgn0000055==Adh</fbsym>

REFDSR
{
RDID|FBrf0091198
|White and Jacobson
|1996
SYN|jockey{}Adh<up>jockey</up>
ASAL|<fbsym>FBal0062209==Adh<up>jockey</up></fbsym>
CLOC|35B3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000055==Adh</fbsym>
}

REF
{
REFM|FBrf0091198
|White and Jacobson
|1996
REFM|FBrf0092724
|White and Jacobson
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015072	ICL 1 P	SYM 1 P{}sn<up>vw</up>	ASTR 1 -	CLOC 1 7D1--2	REF 1 4	DT 1 15 Nov 2000	RESZ 716
ID|FBti0015072
SYM|P{}sn<up>vw</up>
SYN|P{KP}P{}sn<up>vw</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|15 Nov 2000
|6 Jan 2000
ICL|P
ID2|FBti0004422
ASGN|<fbsym>FBgn0003447==sn</fbsym>

REFDSR
{
RDID|FBrf0049839
|Brookfield and Lewis
|1989
SYN|P{}sn<up>vw</up>
ASAL|<fbsym>FBal0062440==sn<up>vw</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REFDSR
{
RDID|FBrf0086933
|Brookfield
|1996
SYN|P{KP}P{}sn<up>vw</up>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REF
{
REFM|FBrf0049839
|Brookfield and Lewis
|1989
REFM|FBrf0074080
|Ortori et al.
|1994
REFM|FBrf0086933
|Brookfield
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0062440==sn<up>vw</up></fbsym>

REFDSR
{
RDID|FBrf0049839
|Brookfield and Lewis
|1989
PHP|Partial revertant; phenotype is almost wild-type, although there are
|patches of <fbsym>FBgn0003447==sn</fbsym> bristles. Somatic reversion of this allele, generating
|patches with a strong <fbsym>FBgn0003447==sn</fbsym> phenotype, occurs at a relatively high frequency.
}

REF
{
REFM|FBrf0049839
|Brookfield and Lewis
|1989
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015085	ICL 1 P	SYM 1 P{}g<up>P</up>	ASTR 1 -	CLOC 1 12B4	REF 1 2	DT 1 6 Jan 2000	RESZ 413
ID|FBti0015085
SYM|P{}g<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0001087==g</fbsym>

REFDSR
{
RDID|FBrf0095986
|Ooi et al.
|1997
SYN|P{}g<up>P</up>
ASAL|<fbsym>FBal0062819==g<up>P</up></fbsym>
CLOC|12B4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001087==g</fbsym>
}

REF
{
REFM|FBrf0095986
|Ooi et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0062819==g<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
PHP|Eye color: red pigments are reduced to 50 +/- 5% of wild-type levels
|in males.
|Testis color: pale yellow (wild-type color is bright yellow).
PHM|pigment cell
|testis sheath
}

REFDSR
{
RDID|FBrf0147069
|Lloyd et al.
|2002
PHP|Homozygotes have 50% red pigment in the eye compared to 100% in wild-type
|flies. <fbsym>FBab0000417==Df(1)HA92</fbsym>/<fbsym>FBal0062819==g<up>P</up></fbsym> flies have lower levels of red
| pigment in
|the eye than <fbsym>FBal0062819==g<up>P</up></fbsym> homozygotes.
PHM|pigment cell
|(with Df(1)HA92) pigment cell
}

REF
{
REFM|FBrf0125153
|Lloyd et al.
|1999
REFM|FBrf0147069
|Lloyd et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015106	ICL 1 P	SYM 1 P{}aop<up>P</up>	ASTR 1 -	CLOC 1 22D1	REF 1 2	DT 1 6 Jan 2000	RESZ 451
ID|FBti0015106
SYM|P{}aop<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0000097==aop</fbsym>

REFDSR
{
RDID|FBrf0096158
|Riesgo-Escovar and Hafen
|1997
SYN|P{}aop<up>P</up>
ASAL|<fbsym>FBal0062981==aop<up>P</up></fbsym>
CLOC|22D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000097==aop</fbsym>
}

REF
{
REFM|FBrf0096158
|Riesgo-Escovar and Hafen
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015161	ICL 1 ?	SYM 1 ?{}stg<up>hwy</up>	ASTR 1 -	CLOC 1 99A5	REF 1 2	DT 1 6 Jan 2000	RESZ 416
ID|FBti0015161
SYM|?{}stg<up>hwy</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0003525==stg</fbsym>

REFDSR
{
RDID|FBrf0111437
|Mozer and Easwarachandran
|1999
SYN|?{}stg<up>hwy</up>
ASAL|<fbsym>FBal0086318==stg<up>hwy</up></fbsym>
CLOC|99A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003525==stg</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111437
|Mozer and Easwarachandran
|1999
}

ALESR
{
ASYM|<fbsym>FBal0086318==stg<up>hwy</up></fbsym>

REFDSR
{
RDID|FBrf0101687
|Stocker and Hafen
|1998
PHP|Homozygotes have bristle and eye defects.  Eye discs contain ectopic
|photoreceptors that are predominantly of the R2/R5 type.
PHM|photoreceptor cell | ectopic
|photoreceptor cell R2 | ectopic
|photoreceptor cell R5 | ectopic
|eye
|macrochaeta
|eye disc
}

REFDSR
{
RDID|FBrf0111437
|Mozer and Easwarachandran
|1999
PHP|Eye of adults are slightly rough and slightly smaller than those of
|wild type. The macrochaetae of the notum are missing. Ommatidia have
|one or more extra photoreceptor cells which may be of any of the inner
|or outer photoreceptor cell types. This phenotype is seen when heterozygous
|with <fbsym>FBal0099818==stg<up>Dr-mr21</up></fbsym>, <fbsym>FBal0099821==stg<up>Dr-FA30</up></fbsym>,
| <fbsym>FBal0035718==stg<up>AR2</up></fbsym> or <fbsym>FBal0035719==stg<up>RXT13</up></fbsym> or
|<fbsym>FBab0024883==Df(3R)Ptp99A<up>R3</up></fbsym>.
|When <fbsym>FBal0086318==stg<up>hwy</up></fbsym> is heterozygous with
| <fbsym>FBal0016176==stg<up>4</up></fbsym> or <fbsym>FBal0016174==stg<up>2</up></fbsym> there
|... (see <fbsym>FBal0086318==stg<up>hwy</up></fbsym> report)
PHM|eye
|macrochaeta
|ommatidium
|photoreceptor cell
|eye disc
}

REF
{
REFM|FBrf0101687
|Stocker and Hafen
|1998
REFM|FBrf0111437
|Mozer and Easwarachandran
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015238	ICL 1 gypsy	SYM 1 gypsy{}ovo<up>Z</up>	ASTR 1 -	CLOC 1 4E2	REF 1 2	DT 1 6 Jan 2000	RESZ 430
ID|FBti0015238
SYM|gypsy{}ovo<up>Z</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0104424
|Dej et al.
|1998
SYN|gypsy{}ovo<up>Z</up>
ASAL|<fbsym>FBal0092576==ovo<up>Z</up></fbsym>
CLOC|4E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003028==ovo</fbsym>
}

REF
{
REFM|FBrf0104424
|Dej et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015239	ICL 1 gypsy	SYM 1 gypsy{}ovo<up>Y</up>	ASTR 1 -	CLOC 1 4E2	REF 1 2	DT 1 6 Jan 2000	RESZ 430
ID|FBti0015239
SYM|gypsy{}ovo<up>Y</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0104424
|Dej et al.
|1998
SYN|gypsy{}ovo<up>Y</up>
ASAL|<fbsym>FBal0092577==ovo<up>Y</up></fbsym>
CLOC|4E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003028==ovo</fbsym>
}

REF
{
REFM|FBrf0104424
|Dej et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015240	ICL 1 gypsy	SYM 1 gypsy{}ovo<up>X</up>	ASTR 1 -	CLOC 1 4E2	REF 1 2	DT 1 6 Jan 2000	RESZ 430
ID|FBti0015240
SYM|gypsy{}ovo<up>X</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|gypsy
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0104424
|Dej et al.
|1998
SYN|gypsy{}ovo<up>X</up>
ASAL|<fbsym>FBal0092578==ovo<up>X</up></fbsym>
CLOC|4E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003028==ovo</fbsym>
}

REF
{
REFM|FBrf0104424
|Dej et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015263	ICL 1 springer	SYM 1 springer{}da<up>lyh</up>	ASTR 1 -	CLOC 1 31D11--E1	REF 1 3	DT 1 6 Jan 2000	RESZ 626
ID|FBti0015263
SYM|springer{}da<up>lyh</up>
ASTP|<fbsym>FBtp0011464==springer</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|springer
ASGN|<fbsym>FBgn0000413==da</fbsym>
ARGS|FBgn0000413

REFDSR
{
RDID|FBrf0107280
|Smith and Cronmiller
|1999
SYN|springer{}da<up>lyh</up>
ASAL|<fbsym>FBal0095470==da<up>lyh</up></fbsym>
CLOC|31D11--E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000413==da</fbsym>
PHC|female sterile
}

REFDSR
{
RDID|FBrf0141491
|Smith and Cronmiller
|2001
PHC|female sterile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107280
|Smith and Cronmiller
|1999
REFM|FBrf0141491
|Smith and Cronmiller
|2001
}

ALESR
{
ASYM|<fbsym>FBal0095470==da<up>lyh</up></fbsym>

REFDSR
{
RDID|FBrf0141491
|Smith and Cronmiller
|2001
PHP|<fbsym>FBal0095470==da<up>lyh</up></fbsym> shows no maternal effects on sex determination
| in complementation
|tests with <fbsym>FBgn0000413==da</fbsym> alleles. <fbsym>FBal0095470==da<up>lyh</up></fbsym> shows no visible
| phenotypes in
|combination with null <fbsym>FBgn0000413==da</fbsym> alleles and deletions.
|Homozygous and <fbsym>FBal0095470==da<up>lyh</up></fbsym>/<fbsym>FBal0002215==da<up>2</up></fbsym>
| ovaries show multiple follicular defects,
|such as missing stalks, multicyst follicles and degeneration of late-stage
|cysts. The phenotype of homozygous ovaries worsens with age.
|<fbsym>FBab0009865==Dp(2;Y)B231</fbsym> ; <fbsym>FBal0095470==da<up>lyh</up></fbsym>/<fbsym>FBal0095470==da<up>lyh</up></fbsym>
| females have ovarioles defects,
|... (see <fbsym>FBal0095470==da<up>lyh</up></fbsym> report)
PHM|egg chamber
|interfollicle cell
|(with da<up>2</up>) egg chamber
|(with da<up>2</up>) interfollicle cell
|(with Dp(2;Y)B231) interfollicle cell
|(with Dp(2;Y)B231) germarium
}

REFDSR
{
RDID|FBrf0148972
|Smith et al.
|2002
PHP|90% of ovarioles have no distinct interfollicle stalks in newly eclosed
|<fbsym>FBal0095470==da<up>lyh</up></fbsym> females. In the remaining 10% of ovarioles,
| the posteriormost
|(first formed) follicle is separated by a stalk from the next youngest
|cyst, but in these cases the second and third cysts of the ovariole
|are always contained in a single continuous epithelium. In older mutant
|females there are extensive defects in the vitellarium, although the
|overall organization of the germarium appears to be undisturbed. There
|... (see <fbsym>FBal0095470==da<up>lyh</up></fbsym> report)
PHM|interfollicle cell
|(with da<up>2</up>) interfollicle cell
|germarium region 2b
|germarium region 3
|germarium
|(with da<up>hs.PSP</up>) follicle cell | conditional ts
|(with da<up>hs.PSP</up>) interfollicle cell | ectopic | conditional ts
|(with Dp(2;Y)B231) female germline stem cell
|(with Dp(2;Y)B231) germline cyst
}

REF
{
REFM|FBrf0141491
|Smith and Cronmiller
|2001
REFM|FBrf0148972
|Smith et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015265	ICL 1 ?	SYM 1 ?{}Dsim\lz<up>L</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 6 Jan 2000	RESZ 410
ID|FBti0015265
SYM|?{}Dsim\lz<up>L</up>
DT|6 Jan 2000
|6 Jan 2000
ICL|?
ASGN|<fbsym>FBgn0018267==Dsim\lz</fbsym>

REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
SYN|?{}Dsim\lz<up>L</up>
ASAL|<fbsym>FBal0095813==Dsim\lz<up>L</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0018267==Dsim\lz</fbsym>
PHC|female sterile | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105876
|Loreto et al.
|1998
}

ALESR
{
ASYM|<fbsym>FBal0095813==Dsim\lz<up>L</up></fbsym>

REFDSR
{
RDID|FBrf0105876
|Loreto et al.
|1998
PHP|The eyes are reduced in size in mutant flies and the surface of the
|eye has a glistening appearance and altered pigmentation. The tarsal
|claws are reduced. Homozygous females are sterile; the spermathecae
|and parovaria are absent.
|Eye color: brown.
PHM|eye
|tarsus
|spermathecal duct
|female accessory gland
}

REF
{
REFM|FBrf0105876
|Loreto et al.
|1998
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015267	ICL 1 roo	SYM 1 roo{}toy<up>roo</up>	ASTR 1 -	CLOC 1 102D1	REF 1 2	DT 1 6 Jan 2000	RESZ 436
ID|FBti0015267
SYM|roo{}toy<up>roo</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|roo
ASGN|<fbsym>FBgn0019650==toy</fbsym>

REFDSR
{
RDID|FBrf0107668
|Czerny et al.
|1999
SYN|roo{}toy<up>roo</up>
ASAL|<fbsym>FBal0096656==toy<up>roo</up></fbsym>
CLOC|102D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0019650==toy</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0107668
|Czerny et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015268	ICL 1 P	SYM 1 P{}ken<up>ok</up>	ASTR 1 -	CLOC 1 60A6--7	REF 1 2	DT 1 24 Aug 2004	RESZ 474
ID|FBti0015268
SYM|P{}ken<up>ok</up>
SYN|P{}ken<up>okina</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|24 Aug 2004
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0011236==ken</fbsym>

REFDSR
{
RDID|FBrf0108232
|Lukacsovich et al.
|1999
SYN|P{}ken<up>okina</up>
ASAL|<fbsym>FBal0096863==ken<up>ok</up></fbsym>
CLOC|60A6--7
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011236==ken</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108232
|Lukacsovich et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0096863==ken<up>ok</up></fbsym>

REFDSR
{
RDID|FBrf0167302
|Lukacsovich et al.
|2003
PHP|8% of homozygous males have aberrant terminalia; some of them appear
|to lack external genitalia, which remain inside the abdominal cuticle.
|Homozygotes have unpigmented aristae.
|The genital disc is malformed in
| <fbsym>FBal0028265==ken<up>1</up></fbsym>/<fbsym>FBal0096863==ken<up>ok</up></fbsym> mutant males and
|some discs are split into two subdivisions.
PHM|male genitalia
|arista
|(with ken<up>00628</up>) terminalia
|(with ken<up>02970</up>) terminalia
|(with ken<up>1</up>) male genital disc
}

REF
{
REFM|FBrf0167302
|Lukacsovich et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015297	ICL 1 P	SYM 1 P{}pAbp<up>duo</up>	ASTR 1 -	CLOC 1 55B8--9	REF 1 2	DT 1 6 Jan 2000	RESZ 443
ID|FBti0015297
SYM|P{}pAbp<up>duo</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|P
ASGN|<fbsym>FBgn0003031==pAbp</fbsym>

REFDSR
{
RDID|FBrf0109692
|Fasulo et al.
|1999
SYN|P{}pAbp<up>duo</up>
ASAL|<fbsym>FBal0099847==pAbp<up>duo</up></fbsym>
CLOC|55B8--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003031==pAbp</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109692
|Fasulo et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0099847==pAbp<up>duo</up></fbsym>

REFDSR
{
RDID|FBrf0109692
|Fasulo et al.
|1999
PHP|The chromosomes in prometaphase and metaphase I meiotic figures of
|mutant males are associated with a minispindle that has the
|appearance of an anastral spindle.  This minispindle is always
|located between the asters but is not connected to them, and its
|orientation, with respect to the axis defined by the asters, is
|quite variable.  The spindle resumes a normal configuration as
|meiosis proceeds, and anaphase does occur.  Defects in both
|... (see <fbsym>FBal0099847==pAbp<up>duo</up></fbsym> report)
PHM|meiotic metaphase I
|meiotic cell cycle
}

REF
{
REFM|FBrf0109692
|Fasulo et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015436	ICL 1 P	SYM 1 P{sE-dos<up>YY</up>}F	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 30 May 2000	RESZ 316
ID|FBti0015436
SYM|P{sE-dos<up>YY</up>}F
SYN|P[sE-dos<up>YY</up>]F
ASTP|<fbsym>FBtp0011796==P{sE-dos<up>YY</up>}</fbsym>
DT|30 May 2000
|3 Feb 2000
ICL|P

REFDSR
{
RDID|FBrf0123046
|Herbst et al.
|1999
SYN|P[sE-dos<up>YY</up>]F
ORI|?
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0123046
|Herbst et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015437	ICL 1 P	SYM 1 P{sE-dos<up>YY</up>}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 30 May 2000	RESZ 316
ID|FBti0015437
SYM|P{sE-dos<up>YY</up>}D
SYN|P[sE-dos<up>YY</up>]D
ASTP|<fbsym>FBtp0011796==P{sE-dos<up>YY</up>}</fbsym>
DT|30 May 2000
|3 Feb 2000
ICL|P

REFDSR
{
RDID|FBrf0123046
|Herbst et al.
|1999
SYN|P[sE-dos<up>YY</up>]D
ORI|?
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0123046
|Herbst et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015503	ICL 1 P	SYM 1 P{lacW}msps<up>P</up>	ASTR 1 -	CLOC 1 89B1--2	REF 1 3	DT 1 4 Feb 2000	RESZ 677
ID|FBti0015503
SYM|P{lacW}msps<up>P</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|4 Feb 2000
|4 Feb 2000
ICL|P
ASGN|<fbsym>FBgn0029100==anon-89Bc</fbsym>
|<fbsym>FBgn0027948==msps</fbsym>

REFDSR
{
RDID|FBrf0111351
|Cullen et al.
|1999
SYN|P{lacW}msps<up>P</up>
ASAL|<fbsym>FBal0102814==anon-89Bc<up>P</up></fbsym>
|<fbsym>FBal0102508==msps<up>P</up></fbsym>
CLOC|89B1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0027948==msps</fbsym>
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0187508
|Brittle and Ohkura
|2005
PHC|lethal | pupal stage
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111351
|Cullen et al.
|1999
REFM|FBrf0187508
|Brittle and Ohkura
|2005
}

ALESR
{
ASYM|<fbsym>FBal0102508==msps<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0111351
|Cullen et al.
|1999
PHP|Homozygotes die around the larval/pupal transition. Third instar larvae
|are superficially normal in size and behavior (they are capable of
|feeding and crawling) although they grow more slowly than wild type.
|The animals die before pupation an no development beyond the early
|pupal stage is seen. The imaginal discs are missing or very small
|in homozygous third instar larvae and the central nervous system is
|also reduced in size. Polytenized tissues, such as the salivary glands
|... (see <fbsym>FBal0102508==msps<up>P</up></fbsym> report)
PHM|mitotic cell cycle
|mitotic anaphase
|mitotic anaphase & nuclear chromosome
|mitotic cell cycle & spindle
}

REFDSR
{
RDID|FBrf0180071
|Moon and Hazelrigg
|2004
PHP|Microtubule organization appears normal in many stage 9 <fbsym>FBal0102508==msps<up>P</up></fbsym>/<fbsym>FBal0135660==msps<up>MJ208</up></fbsym>
|egg chambers. However, some stage 9
| <fbsym>FBal0102508==msps<up>P</up></fbsym>/<fbsym>FBal0135660==msps<up>MJ208</up></fbsym> egg chambers
|have defects in the microtubule cytoskeleton; microtubule density is
|often reduced in the nurse cells and oocyte and the remaining microtubules
|appear disorganized. In addition, whereas in wild-type stage 9 follicle
|cells the density of microtubules is highest at the basal edge of the
|cell, this polarity is lost in the mutant follicle cells.
|... (see <fbsym>FBal0102508==msps<up>P</up></fbsym> report)
PHM|(with msps<up>MJ208</up>) nurse cell & microtubule
|(with msps<up>MJ208</up>) oocyte & microtubule
|(with msps<up>MJ208</up>) follicle cell & microtubule
}

REFDSR
{
RDID|FBrf0187508
|Brittle and Ohkura
|2005
PHP|Haemocytes from mutant larvae show a reduction in the proportion of
|cells with an extended microtubule array, and a rise in the proportion
|of cells with a compact circle of microtubules in the center of the
|cell. Over 60% of haemocytes have a compact microtubule organization,
|compared to 215% in wild-type. Additionally 15% of mutant cells show
|bundling of microtubules, while none are seen in wild-type.
PHM|cytoplasmic microtubule & embryonic/larval hemocyte
}

REF
{
REFM|FBrf0111351
|Cullen et al.
|1999
REFM|FBrf0180071
|Moon and Hazelrigg
|2004
REFM|FBrf0187508
|Brittle and Ohkura
|2005
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015601	ICL 1 ?	SYM 1 ?{}g<up>EMS</up>	ASTR 1 -	CLOC 1 12B4	REF 1 2	DT 1 31 May 2000	RESZ 382
ID|FBti0015601
SYM|?{}g<up>EMS</up>
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|<fbsym>FBgn0001087==g</fbsym>

REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g<up>EMS</up>
ASAL|<fbsym>FBal0004992==g<up>EMS</up></fbsym>
CLOC|12B4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001087==g</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015602	ICL 1 ?	SYM 1 ?{}g<up>im</up>	ASTR 1 -	CLOC 1 12B4	REF 1 2	DT 1 31 May 2000	RESZ 379
ID|FBti0015602
SYM|?{}g<up>im</up>
DT|31 May 2000
|31 May 2000
ICL|?
ASGN|<fbsym>FBgn0001087==g</fbsym>

REFDSR
{
RDID|FBrf0125153
|Lloyd et al.
|1999
SYN|?{}g<up>im</up>
ASAL|<fbsym>FBal0004994==g<up>im</up></fbsym>
CLOC|12B4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001087==g</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125153
|Lloyd et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015735	ICL 1 P	SYM 1 P{PZ}ttk<up>twp</up>	ASTR 1 -	CLOC 1 100D1	REF 1 3	DT 1 31 May 2000	RESZ 539
ID|FBti0015735
SYM|P{PZ}ttk<up>twp</up>
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|31 May 2000
|31 May 2000
ICL|P
ASGN|<fbsym>FBgn0003870==ttk</fbsym>

REFDSR
{
RDID|FBrf0125981
|French and Berg
|2000
PHC|female sterile
}

REFDSR
{
RDID|FBrf0126869
|Berg
|2000.3.7
SYN|P{PZ}ttk<up>twp</up>
ASAL|<fbsym>FBal0104411==ttk<up>twp</up></fbsym>
CLOC|100D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003870==ttk</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125981
|French and Berg
|2000
REFM|FBrf0126869
|Berg
|2000.3.7
}

ALESR
{
ASYM|<fbsym>FBal0104411==ttk<up>twp</up></fbsym>

REFDSR
{
RDID|FBrf0125981
|French and Berg
|2000
PHP|Egg chambers have rudimentary nubs in place of dorsal appendages.
PHM|dorsal appendage
}

REFDSR
{
RDID|FBrf0155483 
PHP|Eggs chambers from homozygous mutant mothers, initiate but fail to
|complete, dorsal appendage morphogenesis. While two appendages initially
|form with proper spacing, these appendages fail to extend to their
|normal length. Up to stage 11 egg chambers have a normal morphology.
|In stage 12 mutant egg chambers, chorion proteins are not deposited
|normally however follicle cells do initiate morphogenesis. the degree
|of cell movement is similar to wild-type at this stage. Stage 13 mutant
|... (see <fbsym>FBal0104411==ttk<up>twp</up></fbsym> report)
PHM|egg chamber | maternal effect
|egg | maternal effect
|dorsal appendage | maternal effect
|follicle cell | maternal effect
|(with Df(3R)awd-KRB) egg chamber | maternal effect
|(with Df(3R)awd-KRB) egg | maternal effect
|(with Df(3R)awd-KRB) dorsal appendage | maternal effect
|(with Df(3R)awd-KRB) follicle cell | maternal effect
|(with ttk<up>1e11</up>) egg chamber | maternal effect
|(with ttk<up>1e11</up>) egg | maternal effect
|(with ttk<up>1e11</up>) dorsal appendage | maternal effect
|(with ttk<up>1e11</up>) follicle cell | maternal effect
|(with ttk<up>1</up>) dorsal appendage | maternal effect
}

REF
{
REFM|FBrf0125981
|French and Berg
|2000
REFM|FBrf0155483 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015749	ICL 1 P	SYM 1 P{lwB}TyrR<up>hono</up>	ASTR 1 -	CLOC 1 79B1--2	REF 1 3	DT 1 19 Nov 2001	RESZ 655
ID|FBti0015749
SYM|P{lwB}TyrR<up>hono</up>
SYN|P{lwB}TyrR<up>hono</up>
|P{lwB}hono<up>hono</up>
ASTP|<fbsym>FBtp0000157==P{lwB}</fbsym>
DT|19 Nov 2001
|31 May 2000
ICL|P
ASGN|<fbsym>FBgn0004514==TyrR</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0126774
|Kutsukake et al.
|2000
SYN|P{lwB}TyrR<up>hono</up>
ASAL|<fbsym>FBal0104845==Ecol\lacZ<up>TyrR-hono</up></fbsym>
|<fbsym>FBal0104701==TyrR<up>hono</up></fbsym>
CLOC|79B1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004514==TyrR</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0049003
|Cooley et al.
|1988
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126774
|Kutsukake et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0104701==TyrR<up>hono</up></fbsym>

REFDSR
{
RDID|FBrf0126774
|Kutsukake et al.
|2000
PHP|The avoidance behavior of <fbsym>FBal0104701==TyrR<up>hono</up></fbsym> flies in response
| to the repellents
|ethyl acetate, benzaldehyde and 4-methylcycrohexanol is impaired compared
|to wild-type flies. Locomotor activity of both males and females is
|normal and slightly increased compared to wild-type flies.
|The excitatory junctional potential of <fbsym>FBal0104701==TyrR<up>hono</up></fbsym>
| larval body wall
|muscles is not inhibited by 10<up>-6</up>M tyramine, in contrast to wild type.
}

REFDSR
{
RDID|FBrf0152276
|Nagaya et al.
|2002
PHP|The enhancement of EJPs by octopamine is similar to that in wild type
|larvae. The inihibitory effect of EJPs by tyramine is completely eliminated.
PHM|neuromuscular junction
}

REF
{
REFM|FBrf0126774
|Kutsukake et al.
|2000
REFM|FBrf0152276
|Nagaya et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0015798	ICL 1 P	SYM 1 P{KP}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Aug 2000	RESZ 364
ID|FBti0015798
SYM|P{KP}D
SYN|KP-D
ASTP|<fbsym>FBtp0011931==P{KP}</fbsym>
DT|15 Aug 2000
|2 Jun 2000
ICL|P

REFDSR
{
RDID|FBrf0058617
|Lemaitre et al.
|1993
SYN|KP-D
CC|Autosomal insertion of <fbsym>FBtp0011931==P{KP}</fbsym>. The KP-D line contains this one autosomal insertion.
}

REF
{
REFM|FBrf0058617
|Lemaitre et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015799	ICL 1 P	SYM 1 P{KP+KP.U}U	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Aug 2000	RESZ 393
ID|FBti0015799
SYM|P{KP+KP.U}U
SYN|KP-U
ASTP|<fbsym>FBtp0012690==P{KP+KP.U}</fbsym>
DT|15 Aug 2000
|2 Jun 2000
ICL|P

REFDSR
{
RDID|FBrf0058617
|Lemaitre et al.
|1993
SYN|KP-U
CC|Autosomal insertion of a nested <fbsym>FBtp0011931==P{KP}</fbsym> element. The KP-U line contains this
| one autosomal insertion.
}

REF
{
REFM|FBrf0058617
|Lemaitre et al.
|1993
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015800	ICL 1 P	SYM 1 P{sev-yan<up>ACT</up>}IVb	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 15 Aug 2000	RESZ 434
ID|FBti0015800
SYM|P{sev-yan<up>ACT</up>}IVb
ASTP|<fbsym>FBtp0001153==P{sev-yan<up>ACT</up>}</fbsym>
DT|15 Aug 2000
|7 Jun 2000
ICL|P
SK|FBst0005791
|w[*]; P{w[+mW.hs]=sev-yan[ACT]}IVb
|Total=1

REFDSR
{
RDID|FBrf0126891
|Bloomington Stock Center
|2000.4.13
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126891
|Bloomington Stock Center
|2000.4.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015801	ICL 1 P	SYM 1 P{sev-yan<up>WT</up>}Ib	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 15 Aug 2000	RESZ 429
ID|FBti0015801
SYM|P{sev-yan<up>WT</up>}Ib
ASTP|<fbsym>FBtp0001154==P{sev-yan<up>WT</up>}</fbsym>
DT|15 Aug 2000
|7 Jun 2000
ICL|P
SK|FBst0005792
|w[*]; P{w[+mW.hs]=sev-yan[WT]}Ib
|Total=1

REFDSR
{
RDID|FBrf0126891
|Bloomington Stock Center
|2000.4.13
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126891
|Bloomington Stock Center
|2000.4.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015802	ICL 1 P	SYM 1 P{GMR-yan<up>ACT</up>}VIa	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 15 Aug 2000	RESZ 430
ID|FBti0015802
SYM|P{GMR-yan<up>ACT</up>}VIa
ASTP|<fbsym>FBtp0001149==P{GMR-yan<up>ACT</up>}</fbsym>
DT|15 Aug 2000
|7 Jun 2000
ICL|P
SK|FBst0005786
|w[*]; P{w[+mC]=GMR-yan[ACT]}VIa
|Total=1

REFDSR
{
RDID|FBrf0126891
|Bloomington Stock Center
|2000.4.13
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126891
|Bloomington Stock Center
|2000.4.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015803	ICL 1 P	SYM 1 P{GMR-yan<up>WT</up>}Ia	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 15 Aug 2000	RESZ 426
ID|FBti0015803
SYM|P{GMR-yan<up>WT</up>}Ia
ASTP|<fbsym>FBtp0001150==P{GMR-yan<up>WT</up>}</fbsym>
DT|15 Aug 2000
|7 Jun 2000
ICL|P
SK|FBst0005787
|w[*]; P{w[+mC]=GMR-yan[WT]}Ia
|Total=1

REFDSR
{
RDID|FBrf0126891
|Bloomington Stock Center
|2000.4.13
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126891
|Bloomington Stock Center
|2000.4.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015842	ICL 1 P	SYM 1 P{wA<up>R</up>}A	ASTR 1 -	CLOC 1 2-	REF 1 2	DT 1 15 Aug 2000	RESZ 314
ID|FBti0015842
SYM|P{wA<up>R</up>}A
SYN|A
ASTP|<fbsym>FBtp0000064==P{wA<up>R</up>}</fbsym>
DT|15 Aug 2000
|8 Jun 2000
ICL|P
PRG|<fbsym>FBti0001828==P{wA<up>R</up>}4-24</fbsym>

REFDSR
{
RDID|FBrf0111794
|Balasov
|1999
SYN|A
ORI|?
CLOC|2-
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111794
|Balasov
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015883	ICL 1 P	SYM 1 P{wA<up>R</up>}XX	ASTR 1 -	CLOC 1 41F1--41F2	REF 1 2	DT 1 15 Aug 2000	RESZ 355
ID|FBti0015883
SYM|P{wA<up>R</up>}XX
SYN|XX
ASTP|<fbsym>FBtp0000064==P{wA<up>R</up>}</fbsym>
DT|15 Aug 2000
|8 Jun 2000
ICL|P
PRG|<fbsym>FBti0001828==P{wA<up>R</up>}4-24</fbsym>

REFDSR
{
RDID|FBrf0111794
|Balasov
|1999
SYN|XX
ORI|?
CLOC|41F1--41F2
|Insertion site 
LOCB|in situ
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111794
|Balasov
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015951	ICL 1 P{M	SYM 1 P{M{peach}w<up>pch</up>}wpch	ASTR 1 -	CLOC 1 1-20	REF 1 3	DT 1 15 Aug 2000	RESZ 603
ID|FBti0015951
SYM|P{M{peach}w<up>pch</up>}wpch
SYN|wpch
ASTP|<fbsym>FBtp0001670==P{M{peach}w<up>pch</up>}</fbsym>
DT|15 Aug 2000
|8 Jun 2000
ICL|P{M

REFDSR
{
RDID|FBrf0054139
|Garza et al.
|1991
ORI|?
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REFDSR
{
RDID|FBrf0125412
|Lohe et al.
|2000
SYN|wpch
ORI|?
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
CC|Located between <fbsym>FBgn0003447==sn</fbsym> and <fbsym>FBgn0002576==lz</fbsym>, at map location 27.0.
}

REF
{
REFM|FBrf0054139
|Garza et al.
|1991
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125412
|Lohe et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015965	ICL 1 P	SYM 1 P{UAS-pro-dronc}W	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Aug 2000	RESZ 294
ID|FBti0015965
SYM|P{UAS-pro-dronc}W
SYN|pro-dronc<up>W</up>
ASTP|<fbsym>FBtp0012455==P{UAS-pro-dronc}</fbsym>
DT|15 Aug 2000
|8 Jun 2000
ICL|P

REFDSR
{
RDID|FBrf0000000Flybase Curation
SYN|pro-dronc<up>W</up>
ORI|?
}

REF
{
REFM|FBrf0000000Flybase Curation
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0015966	ICL 1 P	SYM 1 P{UAS-pro-dronc}S	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Aug 2000	RESZ 294
ID|FBti0015966
SYM|P{UAS-pro-dronc}S
SYN|pro-dronc<up>S</up>
ASTP|<fbsym>FBtp0012455==P{UAS-pro-dronc}</fbsym>
DT|15 Aug 2000
|8 Jun 2000
ICL|P

REFDSR
{
RDID|FBrf0000000Flybase Curation
SYN|pro-dronc<up>S</up>
ORI|?
}

REF
{
REFM|FBrf0000000Flybase Curation
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016044	ICL 1 Dtsa\P	SYM 1 Dtsa\P{}tsa	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Aug 2000	RESZ 839
ID|FBti0016044
SYM|Dtsa\P{}tsa
SYN|P-tsa
DT|15 Aug 2000
|8 Jun 2000
ICL|Dtsa\P

REFDSR
{
RDID|FBrf0111992
|Nouaud et al.
|1999
SYN|P-tsa
ORI|?
CC|The <fbsym>FBti0016044==Dtsa\P{}tsa</fbsym> insertion has resulted in the formation of a new
| transcriptional unit which harbours a de novo synthesis of a new exon and a
| new intron upstream of the original transcription initiation site of the
| <fbsym>FBgn0020464==Dtsa\P-element</fbsym>.  The new exon is constructed from the genomic sequence
| flanking the <fbsym>FBti0016044==Dtsa\P{}tsa</fbsym> insertion, while the first half of the new
| intron is composed of genomic sequence and the second half of the new
| intron is composed of sequence of the <fbsym>FBgn0020464==Dtsa\P-element</fbsym> insertion.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0111992
|Nouaud et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016105	ICL 1 P	SYM 1 P{elavDmORF}elav<up>edr</up>	ASTR 1 -	CLOC 1 -	REF 1 3	DT 1 15 Aug 2000	RESZ 522
ID|FBti0016105
SYM|P{elavDmORF}elav<up>edr</up>
SYN|P{w<up>+</up>=elav<up>+</up>}edr
ASTP|<fbsym>FBtp0005159==P{elavDmORF}</fbsym>
DT|15 Aug 2000
|15 Aug 2000
ICL|P
ASGN|<fbsym>FBgn0000570==elav</fbsym>

REFDSR
{
RDID|FBrf0091103
|Koushika et al.
|1996
ASAL|<fbsym>FBal0057503==elav<up>edr</up></fbsym>
}

REFDSR
{
RDID|FBrf0125219
|Koushika et al.
|2000
SYN|P{w<up>+</up>=elav<up>+</up>}edr
ORI|?
}

REF
{
REFM|FBrf0091103
|Koushika et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0125219
|Koushika et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0057503==elav<up>edr</up></fbsym>

REFDSR
{
RDID|FBrf0091103
|Koushika et al.
|1996
PHP|<fbsym>FBal0003634==elav<up>5</up></fbsym> <fbsym>FBal0057503==elav<up>edr</up></fbsym> flies have
| rough eyes and a disorganized, vacuolar
|retina.
PHM|eye
|retina
}

REF
{
REFM|FBrf0091103
|Koushika et al.
|1996
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0016113	ICL 1 P	SYM 1 P{GawB}waw<up>PTA</up>	ASTR 1 +	CLOC 1 19F5--6	REF 1 1	DT 1 21 Nov 2000	RESZ 947
ID|FBti0016113
SYM|P{GawB}waw<up>PTA</up>
SYN|PTA
|P{UAS-EGFP.M}waw<up>PTA</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|21 Nov 2000
|15 Aug 2000
ICL|P
ASGN|<fbsym>FBgn0024182==waw</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>
ASTR|<fbsym>FBtr0006406==Scer\GAL4<up>waw-PTA</up>RA</fbsym>

REFDSR
{
RDID|FBrf0127238
|Mollereau et al.
|2000
SYN|PTA
ASAL|<fbsym>FBal0118354==Scer\GAL4<up>waw-PTA</up></fbsym>
|<fbsym>FBal0117259==waw<up>PTA</up></fbsym>
ORI|?
CLOC|19F5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0024182==waw</fbsym>
AGT|P{UAS-EGFP.M}
CVBODPC|In adult eye, expression in R7 relatively weak.
CVBODP|transcript distribution deduced from reporter protein distribution, binary system (Gal4 UAS)
|<t> A <a> photoreceptor cell R8 <p>
|<t> A <a> photoreceptor cell R7 <p>
|<t> A <a> adult external thorax <p>
|<t> A <a> scutellum <p>
|<t> A <a> adult external abdomen <p>
}

REF
{
REFM|FBrf0127238
|Mollereau et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016199	ICL 1 P	SYM 1 P{GFP-polo}pX	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 21 Nov 2000	RESZ 350
ID|FBti0016199
SYM|P{GFP-polo}pX
SYN|pX[GFP-POLO]
ASTP|<fbsym>FBtp0012774==P{GFP-polo}</fbsym>
DT|21 Nov 2000
|15 Aug 2000
ICL|P

REFDSR
{
RDID|FBrf0123147
|Moutinho-Santos et al.
|1999
SYN|pX[GFP-POLO]
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0123147
|Moutinho-Santos et al.
|1999
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016846	ICL 1 P	SYM 1 P{GawB}cib<up>P</up>	ASTR 1 -	CLOC 1 4A5	REF 1 3	DT 1 5 Sep 2001	RESZ 644
ID|FBti0016846
SYM|P{GawB}cib<up>P</up>
SYN|P{GAL4}cib<up>P</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|5 Sep 2001
|20 Nov 2000
ICL|P
ASGN|<fbsym>FBgn0026084==cib</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
ASAL|<fbsym>FBal0125285==Scer\GAL4<up>cib-P</up></fbsym>
}

REFDSR
{
RDID|FBrf0129736
|Boquet et al.
|2000
SYN|P{GAL4}cib<up>P</up>
ASAL|<fbsym>FBal0118296==cib<up>P</up></fbsym>
CLOC|4A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0026084==cib</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
REFM|FBrf0129736
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0118296==cib<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|When originally isolated, homozygous adults had a ventrally opened
|ellipsoid body in the central brain with strong penetrance. The penetrance
|became very strong after 5 generations of outcrossing.
|<fbsym>FBal0118296==cib<up>P</up></fbsym>/<fbsym>FBab0000312==Df(1)A113</fbsym> flies have an opened
| ellipsoid body with very
|high frequency.
|Heterozygotes have no adult central brain defect.
PHM|ellipsoid body
|(with Df(1)A113) ellipsoid body
}

REFDSR
{
RDID|FBrf0129736
|Boquet et al.
|2000
PHP|Flies have a mutant ellipsoid body.
PHM|ellipsoid body
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
REFM|FBrf0129736
|Boquet et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0016867	ICL 1 P	SYM 1 P{lacZ-&Dgr;JP}CycE<up>JP</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 21 Nov 2000	RESZ 669
ID|FBti0016867
SYM|P{lacZ-&Dgr;JP}CycE<up>JP</up>
ASTP|<fbsym>FBtp0013216==P{lacZ-&Dgr;JP}</fbsym>
DT|21 Nov 2000
|20 Nov 2000
ICL|P
PRG|<fbsym>FBti0012269==P{lacZ-un3}CycE<up>14.11G</up></fbsym>
ASGN|<fbsym>FBgn0010382==CycE</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0103367
|Secombe et al.
|1998
ASAL|<fbsym>FBal0060748==CycE<up>JP</up></fbsym>
|<fbsym>FBal0092837==Ecol\lacZ<up>CycE-JP</up></fbsym>
CC|Internal deletion of ~4kb within the <fbsym>FBtp0000022==P{lacZ-un3}</fbsym> element in progenitor
| allele <fbsym>FBal0093459==CycE<up>14.11G</up></fbsym>.
}

REF
{
REFM|FBrf0103367
|Secombe et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0060748==CycE<up>JP</up></fbsym>

REFDSR
{
RDID|FBrf0092091
|Secombe et al.
|1997
PHP|Homozygotes have rough eyes as a result of fewer cells entering S
|phase during eye development.
PHM|eye
}

REFDSR
{
RDID|FBrf0103367
|Secombe et al.
|1998
PHP|Homozygotes have small, rough eyes. Disorganization in the arrangement
|of ommatidia, blistering on the eye surface and defects in eye bristle
|number and arrangement are seen. Pigment cells surrounding the photoreceptor
|cells are reduced in number or absent, resulting in fusion of ommatidia.
|The number and arrangement of photoreceptor cells in each ommatidium
|is usually normal, although occasionally ommatidia containing less
|than 7 photoreceptor cells are seen. Eye discs are smaller than in
|... (see <fbsym>FBal0060748==CycE<up>JP</up></fbsym> report)
PHM|eye
|wing vein L5
|wing | posterior | distal
|ommatidium
|interommatidial bristle
|pigment cell
|photoreceptor cell
|eye disc
}

REFDSR
{
RDID|FBrf0105843
|Horsfield et al.
|1998
PHP|Rough eye phenotype. Eyes are small and ommatidia are fused.
PHM|eye
|ommatidium
}

REFDSR
{
RDID|FBrf0138503
|Moberg et al.
|2001
PHP|Mutants have a rough eye phenotype.
PHM|eye
}

REFDSR
{
RDID|FBrf0151282
|Brumby et al.
|2002
PHP|Mutant animals have a rough eye phenotype. Homozygous mutant animals
|have notched wings, as well as missing hairs along the posterior/distal
|wing margin, the missing hairs along the posterior/proximal wing blade
|and shortening of wing vein L5.
PHM|eye
|wing
|wing hair
|wing vein L5
}

REFDSR
{
RDID|FBrf0158863
|Doronkin et al.
|2003
PHP|8.6 % of egg chambers in <fbsym>FBal0060748==CycE<up>JP</up></fbsym> homozygotes have
| half the normal
|number of germ-line cells.
|37.7% of egg chambers in
| <fbsym>FBal0060748==CycE<up>JP</up></fbsym>/<fbsym>FBal0033578==CycE<up>AR95</up></fbsym> flies
| raised at 18<up>o</up>C,
|have half the normal number of germ-line cells.
PHM|nurse cell
|(with CycE<up>AR95</up>) nurse cell
}

REFDSR
{
RDID|FBrf0161987
|Wu et al.
|2003
PHP|<fbsym>FBal0033578==CycE<up>AR95</up></fbsym>/<fbsym>FBal0060748==CycE<up>JP</up></fbsym> animals have
| small, rough eyes.
PHM|(with CycE<up>AR95</up>) eye
|(with CycE<up>AR95</up>) ommatidium
}

REFDSR
{
RDID|FBrf0180290
|Zraly et al.
|2004
PHM|eye
|wing
}

REFDSR
{
RDID|FBrf0180291
|Brumby et al.
|2004
PHP|Homozygotes have a rough eye phenotype.
PHM|eye
|ommatidium
}

REF
{
REFM|FBrf0092091
|Secombe et al.
|1997
REFM|FBrf0103367
|Secombe et al.
|1998
REFM|FBrf0105843
|Horsfield et al.
|1998
REFM|FBrf0138503
|Moberg et al.
|2001
REFM|FBrf0151282
|Brumby et al.
|2002
REFM|FBrf0158863
|Doronkin et al.
|2003
REFM|FBrf0161987
|Wu et al.
|2003
REFM|FBrf0180290
|Zraly et al.
|2004
REFM|FBrf0180291
|Brumby et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0016886	ICL 1 P	SYM 1 P{UAS-Dp.D}III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 26 Dec 2000	RESZ 273
ID|FBti0016886
SYM|P{UAS-Dp.D}III
SYN|UAS-DP(III)
ASTP|<fbsym>FBtp0001662==P{UAS-Dp.D}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P

REFDSR
{
RDID|FBrf0129782
|Datar et al.
|2000
SYN|UAS-DP(III)
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129782
|Datar et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016887	ICL 1 P	SYM 1 P{UAS-CycE.L}III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 26 Dec 2000	RESZ 281
ID|FBti0016887
SYM|P{UAS-CycE.L}III
SYN|UAS-CycE(III)
ASTP|<fbsym>FBtp0001368==P{UAS-CycE.L}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P

REFDSR
{
RDID|FBrf0129782
|Datar et al.
|2000
SYN|UAS-CycE(III)
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129782
|Datar et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016888	ICL 1 P	SYM 1 P{UAS-Rbf.D}III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 26 Dec 2000	RESZ 277
ID|FBti0016888
SYM|P{UAS-Rbf.D}III
SYN|UAS-RBF(III)
ASTP|<fbsym>FBtp0001663==P{UAS-Rbf.D}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P

REFDSR
{
RDID|FBrf0129782
|Datar et al.
|2000
SYN|UAS-RBF(III)
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129782
|Datar et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016942	ICL 1 P	SYM 1 P{UAS-proPO}X	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 26 Dec 2000	RESZ 390
ID|FBti0016942
SYM|P{UAS-proPO}X
ASTP|<fbsym>FBtp0013487==P{UAS-proPO}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P
SK|FBst0005866
|P{w[+mC]=UAS-proPO}X, y[1] w[*]
|Total=1

REFDSR
{
RDID|FBrf0132164
|True et al.
|2000.10.19
ORI|?
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0132164
|True et al.
|2000.10.19
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016949	ICL 1 P	SYM 1 P{UAS-Su(H).K}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 26 Dec 2000	RESZ 303
ID|FBti0016949
SYM|P{UAS-Su(H).K}II
ASTP|<fbsym>FBtp0013369==P{UAS-Su(H).K}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P

REFDSR
{
RDID|FBrf0128529
|Klein et al.
|2000
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128529
|Klein et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016950	ICL 1 P	SYM 1 P{UAS-Su(H).K}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 26 Dec 2000	RESZ 305
ID|FBti0016950
SYM|P{UAS-Su(H).K}III
ASTP|<fbsym>FBtp0013369==P{UAS-Su(H).K}</fbsym>
DT|26 Dec 2000
|22 Dec 2000
ICL|P

REFDSR
{
RDID|FBrf0128529
|Klein et al.
|2000
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128529
|Klein et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0016959	ICL 1 P	SYM 1 P{lacW}slmb<up>crd</up>	ASTR 1 -	CLOC 1 93B13--C1	REF 1 2	DT 1 25 Dec 2000	RESZ 490
ID|FBti0016959
SYM|P{lacW}slmb<up>crd</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|25 Dec 2000
|25 Dec 2000
ICL|P
ASGN|<fbsym>FBgn0023423==slmb</fbsym>

REFDSR
{
RDID|FBrf0130171
|Wojcik et al.
|2000
SYN|P{lacW}slmb<up>crd</up>
ASAL|<fbsym>FBal0104425==slmb<up>crd</up></fbsym>
CLOC|93B13--C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0023423==slmb</fbsym>
PHC|lethal | pupal stage | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0130171
|Wojcik et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0104425==slmb<up>crd</up></fbsym>

REFDSR
{
RDID|FBrf0126489
|Wojcik and Hays
|2000
PHP|Affected cells have additional centrosomes and mitotic defects.
PHM|mitotic cell cycle
|centrosome | ectopic
}

REFDSR
{
RDID|FBrf0130171
|Wojcik et al.
|2000
PHP|The majority of hemizygous mutant neuroblasts exhibit an excessive
|number of centrosomes. Diploid cells are observed that contain more
|than two and as many as seventeen centrosomes. Polyploid giant neuroblasts
|are also observed in mutant brain discs and they contain far greater
|numbers of centrosomes than predicted by failure in cleavage alone.
|74% of those cells with abnormal numbers of centrosomes have even
|numbers of centrosomes. Despite such aberrant centrosomes, the spindles
|... (see <fbsym>FBal0104425==slmb<up>crd</up></fbsym> report)
PHM|centrosome & neuroblast
|mitotic cell cycle & neuroblast
}

REF
{
REFM|FBrf0126489
|Wojcik and Hays
|2000
REFM|FBrf0130171
|Wojcik et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0016960	ICL 1 P	SYM 1 P{wA<up>R</up>}w<up>A</up>	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 25 Dec 2000	RESZ 471
ID|FBti0016960
SYM|P{wA<up>R</up>}w<up>A</up>
SYN|Line A
ASTP|<fbsym>FBtp0000064==P{wA<up>R</up>}</fbsym>
DT|25 Dec 2000
|25 Dec 2000
ICL|P
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0129721
|Balasov et al.
|2000
SYN|Line A
|P{wA<up>R</up>}w<up>A</up>
ASAL|<fbsym>FBal0119091==w<up>A</up></fbsym>
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129721
|Balasov et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0119091==w<up>A</up></fbsym>

REFDSR
{
RDID|FBrf0129721
|Balasov et al.
|2000
PHP|Exhibits mosaic expression of the <fbsym>FBgn0003996==w</fbsym> gene. The number of colored
|facets in these flies is reduced by either lowering the temperature
|or removing the Y chromosome.
PHM|pigment cell
}

REF
{
REFM|FBrf0129721
|Balasov et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0016967	ICL 1 ?	SYM 1 ?{}ci<up>n</up>	ASTR 1 -	CLOC 1 102A1--3	REF 1 2	DT 1 25 Dec 2000	RESZ 493
ID|FBti0016967
SYM|?{}ci<up>n</up>
DT|25 Dec 2000
|25 Dec 2000
ICL|?
ASGN|<fbsym>FBgn0004859==ci</fbsym>

REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
SYN|?{}ci<up>n</up>
ASAL|<fbsym>FBal0119295==ci<up>n</up></fbsym>
CLOC|102A1--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004859==ci</fbsym>
PHC|(with ci<up>D</up>) lethal | pupal stage
|(with ci<up>94</up>) lethal | pupal stage
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}

ALESR
{
ASYM|<fbsym>FBal0119295==ci<up>n</up></fbsym>

REFDSR
{
RDID|FBrf0129753
|Campbell and Tomlinson
|2000
PHP|A small percentage of flies have wing duplications and most flies have
|enlarged antennae.
|<fbsym>FBal0119295==ci<up>n</up></fbsym>/<fbsym>FBal0045443==ci<up>94</up></fbsym> imaginal discs show overgrowth.
PHM|wing
|antenna
|(with ci<up>94</up>) ventral thoracic disc
|(with ci<up>94</up>) dorsal mesothoracic disc
}

REF
{
REFM|FBrf0129753
|Campbell and Tomlinson
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017048	ICL 1 P	SYM 1 P{EP}lea<up>EP</up>	ASTR 1 -	CLOC 1 22A1	REF 1 2	DT 1 4 Sep 2001	RESZ 498
ID|FBti0017048
SYM|P{EP}lea<up>EP</up>
SYN|EProbo2
|P{EP}robo2<up>EP</up>
|P{}robo2<up>EP</up>
ASTP|<fbsym>FBtp0001317==P{EP}</fbsym>
DT|4 Sep 2001
|19 Feb 2001
ICL|P
ASGN|<fbsym>FBgn0002543==lea</fbsym>

REFDSR
{
RDID|FBrf0128391
|Bashaw et al.
|2000
SYN|EProbo2
|P{}robo2<up>EP</up>
ASAL|<fbsym>FBal0120370==lea<up>EP</up></fbsym>
CLOC|22A1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002543==lea</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128391
|Bashaw et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0120370==lea<up>EP</up></fbsym>

REFDSR
{
RDID|FBrf0128391
|Bashaw et al.
|2000
PHP|Expression of <fbsym>FBal0120370==lea<up>EP</up></fbsym> when driven by <fbsym>FBal0052396==Scer\GAL4<up>unspecified</up></fbsym>,
|causes a loss of commissure phenotype.
PHM|commissure with <fbsym>FBal0052396==Scer\GAL4<up>unspecified</up></fbsym>
}

REF
{
REFM|FBrf0128391
|Bashaw et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017270	ICL 1 Doc	SYM 1 Doc{}plx<up>Doc</up>	ASTR 1 -	CLOC 1 83C1	REF 1 2	DT 1 1 May 2001	RESZ 433
ID|FBti0017270
SYM|Doc{}plx<up>Doc</up>
ASTP|<fbsym>FBtp0011424==Doc</fbsym>
DT|1 May 2001
|1 May 2001
ICL|Doc
ASGN|<fbsym>FBgn0004879==plx</fbsym>

REFDSR
{
RDID|FBrf0087805
|Zhang et al.
|1996
SYN|Doc{}plx<up>Doc</up>
ASAL|<fbsym>FBal0121603==plx<up>Doc</up></fbsym>
CLOC|83C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004879==plx</fbsym>
}

REF
{
REFM|FBrf0087805
|Zhang et al.
|1996
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017291	ICL 1 P	SYM 1 P{}Pkn<up>delorean</up>	ASTR 1 -	CLOC 1 45C1	REF 1 2	DT 1 1 May 2001	RESZ 485
ID|FBti0017291
SYM|P{}Pkn<up>delorean</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|1 May 2001
|1 May 2001
ICL|P
ASGN|<fbsym>FBgn0020621==Pkn</fbsym>

REFDSR
{
RDID|FBrf0133469
|Ostrow and Momin
|2001
SYN|P{}Pkn<up>delorean</up>
ASAL|<fbsym>FBal0122034==Pkn<up>delorean</up></fbsym>
CLOC|45C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0020621==Pkn</fbsym>
PHC|male sterile | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0133469
|Ostrow and Momin
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122034==Pkn<up>delorean</up></fbsym>

REFDSR
{
RDID|FBrf0133469
|Ostrow and Momin
|2001
PHP|Homozygotes have wings that stand up from the thorax and curve
|down.  The phenotype also manifests itself in mechanosensory
|bristles of the anterior wing margins.
PHM|wing
|wing margin bristle
}

REF
{
REFM|FBrf0133469
|Ostrow and Momin
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017296	ICL 1 P	SYM 1 P{EP}flexin<up>EP</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 1 May 2001	RESZ 416
ID|FBti0017296
SYM|P{EP}flexin<up>EP</up>
ASTP|<fbsym>FBtp0001317==P{EP}</fbsym>
DT|1 May 2001
|1 May 2001
ICL|P
ASGN|<fbsym>FBgn0042643==flexin</fbsym>

REFDSR
{
RDID|FBrf0128626
|Roos et al.
|2000
SYN|P{EP}flexin<up>EP</up>
ASAL|<fbsym>FBal0118245==flexin<up>EP</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0042643==flexin</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0128626
|Roos et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0118245==flexin<up>EP</up></fbsym>

REFDSR
{
RDID|FBrf0128626
|Roos et al.
|2000
PHP|Overexpression of <fbsym>FBal0118245==flexin<up>EP</up></fbsym> (driven by
|<fbsym>FBal0052396==Scer\GAL4<up>unspecified</up></fbsym>) in muscle during postembryonic development
|causes a dramatic increase in nerve-terminal branching.  There is a
|two-fold increase in the occurrence of microtubule loops.
PHM|synapse with <fbsym>FBal0052396==Scer\GAL4<up>unspecified</up></fbsym>
}

REF
{
REFM|FBrf0128626
|Roos et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017297	ICL 1 P	SYM 1 P{Mhc-lacZ.H}CyO	ASTR 1 -	CLOC 1 2-	REF 1 2	DT 1 1 May 2001	RESZ 355
ID|FBti0017297
SYM|P{Mhc-lacZ.H}CyO
ASTP|<fbsym>FBtp0004413==P{Mhc-lacZ.H}</fbsym>
DT|1 May 2001
|1 May 2001
ICL|P

REFDSR
{
RDID|FBrf0131298
|Ghazi et al.
|2000
SYN|P{Mhc-lacZ.H}CyO
CLOC|2-
ABA|Balancer <fbsym>FBba0000349==CyO-Mhc-lacZ</fbsym>
CH|insertion on balancer | 2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0131298
|Ghazi et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017411	ICL 1 P	SYM 1 P{hs-mtSSB.M}B	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 1 May 2001	RESZ 320
ID|FBti0017411
SYM|P{hs-mtSSB.M}B
SYN|line B
ASTP|<fbsym>FBtp0013853==P{hs-mtSSB.M}</fbsym>
DT|1 May 2001
|1 May 2001
ICL|P

REFDSR
{
RDID|FBrf0135257
|Maier et al.
|2001
SYN|line B
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135257
|Maier et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017412	ICL 1 P	SYM 1 P{hs-mtSSB.M}D	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 1 May 2001	RESZ 320
ID|FBti0017412
SYM|P{hs-mtSSB.M}D
SYN|line D
ASTP|<fbsym>FBtp0013853==P{hs-mtSSB.M}</fbsym>
DT|1 May 2001
|1 May 2001
ICL|P

REFDSR
{
RDID|FBrf0135257
|Maier et al.
|2001
SYN|line D
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135257
|Maier et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017445	ICL 1 P	SYM 1 P{SUPor-P}wapl<up>Scim</up>	ASTR 1 -	CLOC 1 2D4--5	REF 1 2	DT 1 4 Jun 2001	RESZ 458
ID|FBti0017445
SYM|P{SUPor-P}wapl<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0004655==wapl</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}wapl<up>Scim</up>
ASAL|<fbsym>FBal0122874==wapl<up>Scim</up></fbsym>
CLOC|2D4--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004655==wapl</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122874==wapl<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 19%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017446	ICL 1 P	SYM 1 P{SUPor-P}sca<up>Scim-b</up>	ASTR 1 -	CLOC 1 49C3--D3	REF 1 2	DT 1 4 Jun 2001	RESZ 461
ID|FBti0017446
SYM|P{SUPor-P}sca<up>Scim-b</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0003326==sca</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}sca<up>Scim-b</up>
ASAL|<fbsym>FBal0122912==sca<up>Scim-b</up></fbsym>
CLOC|49C3--D3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003326==sca</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122912==sca<up>Scim-b</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 20%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017447	ICL 1 P	SYM 1 P{SUPor-P}sca<up>Scim-a</up>	ASTR 1 -	CLOC 1 49C3--D3	REF 1 2	DT 1 4 Jun 2001	RESZ 461
ID|FBti0017447
SYM|P{SUPor-P}sca<up>Scim-a</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0003326==sca</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}sca<up>Scim-a</up>
ASAL|<fbsym>FBal0122913==sca<up>Scim-a</up></fbsym>
CLOC|49C3--D3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003326==sca</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122913==sca<up>Scim-a</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 17%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017448	ICL 1 P	SYM 1 P{SUPor-P}pav<up>Scim</up>	ASTR 1 -	CLOC 1 64A10--11	REF 1 2	DT 1 4 Jun 2001	RESZ 497
ID|FBti0017448
SYM|P{SUPor-P}pav<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0011692==pav</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}pav<up>Scim</up>
ASAL|<fbsym>FBal0122937==pav<up>Scim</up></fbsym>
CLOC|64A10--11
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011692==pav</fbsym>
PHC|lethal | embryonic stage | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122937==pav<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 18%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017449	ICL 1 P	SYM 1 P{SUPor-P}oaf<up>Scim-b</up>	ASTR 1 -	CLOC 1 22F4	REF 1 2	DT 1 4 Jun 2001	RESZ 457
ID|FBti0017449
SYM|P{SUPor-P}oaf<up>Scim-b</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0011818==oaf</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}oaf<up>Scim-b</up>
ASAL|<fbsym>FBal0122940==oaf<up>Scim-b</up></fbsym>
CLOC|22F4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011818==oaf</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122940==oaf<up>Scim-b</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 20%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017450	ICL 1 P	SYM 1 P{SUPor-P}oaf<up>Scim-a</up>	ASTR 1 -	CLOC 1 22F4	REF 1 2	DT 1 4 Jun 2001	RESZ 545
ID|FBti0017450
SYM|P{SUPor-P}oaf<up>Scim-a</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0011818==oaf</fbsym>
SK|FBst0014795
|y[1]; P{y[+mDint2] w[BR.E.BR]=SUPor-P}oaf[Scim-a]/SM1; ry[506]
|Total=1

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}oaf<up>Scim-a</up>
ASAL|<fbsym>FBal0122941==oaf<up>Scim-a</up></fbsym>
CLOC|22F4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011818==oaf</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122941==oaf<up>Scim-a</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 20%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017454	ICL 1 P	SYM 1 P{SUPor-P}grp<up>Scim</up>	ASTR 1 -	CLOC 1 36A10	REF 1 2	DT 1 4 Jun 2001	RESZ 452
ID|FBti0017454
SYM|P{SUPor-P}grp<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0011598==grp</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}grp<up>Scim</up>
ASAL|<fbsym>FBal0122971==grp<up>Scim</up></fbsym>
CLOC|36A10
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011598==grp</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0122971==grp<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|The <fbsym>FBal0122971==grp<up>Scim</up></fbsym>, <fbsym>FBal0123092==Scim12<up>4</up></fbsym> double
| mutant chromosome dominantly decreases
|transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring to 17%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017458	ICL 1 P	SYM 1 P{SUPor-P}cnn<up>Scim</up>	ASTR 1 -	CLOC 1 50A8--9	REF 1 2	DT 1 4 Jun 2001	RESZ 454
ID|FBti0017458
SYM|P{SUPor-P}cnn<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0013765==cnn</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}cnn<up>Scim</up>
ASAL|<fbsym>FBal0123015==cnn<up>Scim</up></fbsym>
CLOC|50A8--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0013765==cnn</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123015==cnn<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 17%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017459	ICL 1 P	SYM 1 P{SUPor-P}bif<up>Scim</up>	ASTR 1 -	CLOC 1 10D4--5	REF 1 2	DT 1 4 Jun 2001	RESZ 535
ID|FBti0017459
SYM|P{SUPor-P}bif<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0014133==bif</fbsym>
SK|FBst0014571
|y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}bif[Scim]; ry[506]
|Total=1

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}bif<up>Scim</up>
ASAL|<fbsym>FBal0123031==bif<up>Scim</up></fbsym>
CLOC|10D4--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0014133==bif</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123031==bif<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 16%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017513	ICL 1 P	SYM 1 P{SUPor-P}LanA<up>Scim</up>	ASTR 1 -	CLOC 1 65A8--9	REF 1 2	DT 1 4 Jun 2001	RESZ 541
ID|FBti0017513
SYM|P{SUPor-P}LanA<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0002526==LanA</fbsym>
SK|FBst0014568
|y[1]; P{y[+mDint2] w[BR.E.BR]=SUPor-P}LanA[Scim] ry[506]
|Total=1

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}LanA<up>Scim</up>
ASAL|<fbsym>FBal0123144==LanA<up>Scim</up></fbsym>
CLOC|65A8--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002526==LanA</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123144==LanA<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 14%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017517	ICL 1 P	SYM 1 P{SUPor-P}Gli<up>Scim</up>	ASTR 1 -	CLOC 1 35D4	REF 1 2	DT 1 4 Jun 2001	RESZ 451
ID|FBti0017517
SYM|P{SUPor-P}Gli<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0001987==Gli</fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}Gli<up>Scim</up>
ASAL|<fbsym>FBal0123167==Gli<up>Scim</up></fbsym>
CLOC|35D4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001987==Gli</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123167==Gli<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 19%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017520	ICL 1 P	SYM 1 P{SUPor-P}Fim<up>Scim</up>	ASTR 1 -	CLOC 1 15F8--16A1	REF 1 2	DT 1 4 Jun 2001	RESZ 538
ID|FBti0017520
SYM|P{SUPor-P}Fim<up>Scim</up>
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
ASGN|<fbsym>FBgn0024238==Fim</fbsym>
SK|FBst0014564
|y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}Fim[Scim]; ry[506]
|Total=1

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
SYN|P{SUPor-P}Fim<up>Scim</up>
ASAL|<fbsym>FBal0123170==Fim<up>Scim</up></fbsym>
CLOC|15F8--16A1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0024238==Fim</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135802
|Dobie et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123170==Fim<up>Scim</up></fbsym>

REFDSR
{
RDID|FBrf0135802
|Dobie et al.
|2001
PHP|Dominantly decreases transmission of <fbsym>FBab0024065==Dp(1;f)J21A</fbsym> to offspring
|to 19%.
}

REF
{
REFM|FBrf0135802
|Dobie et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0017539	ICL 1 P	SYM 1 P{hs-hid}Y	ASTR 1 -	CLOC 1 Y	REF 1 2	DT 1 4 Jun 2001	RESZ 339
ID|FBti0017539
SYM|P{hs-hid}Y
SYN|phs-hidY
ASTP|<fbsym>FBtp0001389==P{hs-hid}</fbsym>
DT|4 Jun 2001
|4 Jun 2001
ICL|P
SK|FBst0008846
|w[*]; Dp(2;Y)G, P{w[+mC]=hs-hid}Y
|Total=1

REFDSR
{
RDID|FBrf0134584
|Starz-Gaiano et al.
|2001
SYN|phs-hidY
CLOC|Y
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0134584
|Starz-Gaiano et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017779	ICL 1 P	SYM 1 P{Winkelried}D	ASTR 1 -	CLOC 1 21-60	REF 1 3	DT 1 5 Sep 2001	RESZ 403
ID|FBti0017779
SYM|P{Winkelried}D
SYN|Wink-D
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0134593
|Seum et al.
|2001
SYN|Wink-D
}

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0134593
|Seum et al.
|2001
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017784	ICL 1 P	SYM 1 P{UAS-g/reaper}XA	ASTR 1 -	CLOC 1 X	REF 1 2	DT 1 23 Jul 2001	RESZ 299
ID|FBti0017784
SYM|P{UAS-g/reaper}XA
SYN|P[UAS-g/reaper]-XA
ASTP|<fbsym>FBtp0014385==P{UAS-g/reaper}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135877
|Wing et al.
|2001
SYN|P[UAS-g/reaper]-XA
CLOC|X
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135877
|Wing et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017798	ICL 1 P	SYM 1 P{UAS-rpr.C.W}X	ASTR 1 -	CLOC 1 X	REF 1 2	DT 1 23 Jul 2001	RESZ 294
ID|FBti0017798
SYM|P{UAS-rpr.C.W}X
SYN|P[UAS-reaper-C-X]
ASTP|<fbsym>FBtp0014321==P{UAS-rpr.C.W}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0105960
|Wing et al.
|2001
SYN|P[UAS-reaper-C-X]
CLOC|X
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105960
|Wing et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017828	ICL 1 P	SYM 1 P{EGNPA}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017828
SYM|P{EGNPA}D
SYN|D
ASTP|<fbsym>FBtp0014389==P{EGNPA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|D
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017829	ICL 1 P	SYM 1 P{EGNPA}F	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017829
SYM|P{EGNPA}F
SYN|F
ASTP|<fbsym>FBtp0014389==P{EGNPA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|F
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017830	ICL 1 P	SYM 1 P{EGNPA}G	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017830
SYM|P{EGNPA}G
SYN|G
ASTP|<fbsym>FBtp0014389==P{EGNPA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|G
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017831	ICL 1 P	SYM 1 P{EGNPA}L	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017831
SYM|P{EGNPA}L
SYN|L
ASTP|<fbsym>FBtp0014389==P{EGNPA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|L
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017832	ICL 1 P	SYM 1 P{EGNPA}J	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017832
SYM|P{EGNPA}J
SYN|J
ASTP|<fbsym>FBtp0014389==P{EGNPA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|J
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017833	ICL 1 P	SYM 1 P{EGNAY}C	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017833
SYM|P{EGNAY}C
SYN|C
ASTP|<fbsym>FBtp0014391==P{EGNAY}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|C
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017834	ICL 1 P	SYM 1 P{EGNAY}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017834
SYM|P{EGNAY}D
SYN|D
ASTP|<fbsym>FBtp0014391==P{EGNAY}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|D
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017835	ICL 1 P	SYM 1 P{EGNAY}E	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017835
SYM|P{EGNAY}E
SYN|E
ASTP|<fbsym>FBtp0014391==P{EGNAY}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|E
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017836	ICL 1 P	SYM 1 P{EGN&Dgr;LFK}A	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 265
ID|FBti0017836
SYM|P{EGN&Dgr;LFK}A
SYN|A
ASTP|<fbsym>FBtp0014392==P{EGN&Dgr;LFK}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|A
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017837	ICL 1 P	SYM 1 P{EGN&Dgr;LFK}G	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 265
ID|FBti0017837
SYM|P{EGN&Dgr;LFK}G
SYN|G
ASTP|<fbsym>FBtp0014392==P{EGN&Dgr;LFK}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|G
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017838	ICL 1 P	SYM 1 P{EGN&Dgr;LFK}H	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 265
ID|FBti0017838
SYM|P{EGN&Dgr;LFK}H
SYN|H
ASTP|<fbsym>FBtp0014392==P{EGN&Dgr;LFK}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|H
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017839	ICL 1 P	SYM 1 P{EGNHA}A	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017839
SYM|P{EGNHA}A
SYN|A
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|A
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017840	ICL 1 P	SYM 1 P{EGNHA}C	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017840
SYM|P{EGNHA}C
SYN|C
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|C
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017841	ICL 1 P	SYM 1 P{EGNHA}F	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017841
SYM|P{EGNHA}F
SYN|F
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|F
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017842	ICL 1 P	SYM 1 P{EGNHA}G	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017842
SYM|P{EGNHA}G
SYN|G
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|G
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017843	ICL 1 P	SYM 1 P{EGNHA}M	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017843
SYM|P{EGNHA}M
SYN|M
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|M
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017844	ICL 1 P	SYM 1 P{EGNHA}N	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017844
SYM|P{EGNHA}N
SYN|N
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|N
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017845	ICL 1 P	SYM 1 P{EGNHA}S	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017845
SYM|P{EGNHA}S
SYN|S
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|S
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017846	ICL 1 P	SYM 1 P{EGNHA}T	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017846
SYM|P{EGNHA}T
SYN|T
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|T
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017847	ICL 1 P	SYM 1 P{EGNHA}W	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 253
ID|FBti0017847
SYM|P{EGNHA}W
SYN|W
ASTP|<fbsym>FBtp0014390==P{EGNHA}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135733
|Kobayashi et al.
|2001
SYN|W
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135733
|Kobayashi et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0017855	ICL 1 P	SYM 1 P{dsh.EGFP}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 23 Jul 2001	RESZ 335
ID|FBti0017855
SYM|P{dsh.EGFP}II
SYN|dsh::GFP<up>II</up>
ASTP|<fbsym>FBtp0014396==P{dsh.EGFP}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0135774
|Axelrod
|2001
SYN|dsh::GFP<up>II</up>
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135774
|Axelrod
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018001	ICL 1 P	SYM 1 P{UAS-AUG-DsRed}A	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 23 Jul 2001	RESZ 407
ID|FBti0018001
SYM|P{UAS-AUG-DsRed}A
ASTP|<fbsym>FBtp0014535==P{UAS-AUG-DsRed}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
SK|FBst0006282
|w[*]; P{w[+mC]=UAS-AUG-DsRed}A
|Total=1

REFDSR
{
RDID|FBrf0136779
|Kasuya and Iverson
|2000.11.13
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136779
|Kasuya and Iverson
|2000.11.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018002	ICL 1 P	SYM 1 P{UAS-AUG-DsRed}B	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 23 Jul 2001	RESZ 519
ID|FBti0018002
SYM|P{UAS-AUG-DsRed}B
ASTP|<fbsym>FBtp0014535==P{UAS-AUG-DsRed}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
SK|FBst0006281
|w[*]; P{w[+mC]=UAS-AUG-DsRed}B/CyO, P{ry[+t7.2]=sevRas1.V12}FK1
|Total=1

REFDSR
{
RDID|FBrf0136779
|Kasuya and Iverson
|2000.11.13
SYN|P{UAS-AUG-DsRed}B
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
PHC|viable
CC|Chromosome is associated with an undefined recessive sterility.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136779
|Kasuya and Iverson
|2000.11.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018003	ICL 1 P	SYM 1 P{UAS-AUG-DsRed}Ea	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 23 Jul 2001	RESZ 438
ID|FBti0018003
SYM|P{UAS-AUG-DsRed}Ea
ASTP|<fbsym>FBtp0014535==P{UAS-AUG-DsRed}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
SK|FBst0006280
|P{w[+mC]=UAS-AUG-DsRed}Ea, w[*]; P{UAS-AUG-DsRed}Eb; P{UAS-AUG-DsRed}Ec
|Total=1

REFDSR
{
RDID|FBrf0136779
|Kasuya and Iverson
|2000.11.13
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
PHC|viable
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136779
|Kasuya and Iverson
|2000.11.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018004	ICL 1 P	SYM 1 P{UAS-AUG-DsRed}Eb	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 23 Jul 2001	RESZ 428
ID|FBti0018004
SYM|P{UAS-AUG-DsRed}Eb
ASTP|<fbsym>FBtp0014535==P{UAS-AUG-DsRed}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
SK|FBst0006280
|P{w[+mC]=UAS-AUG-DsRed}Ea, w[*]; P{UAS-AUG-DsRed}Eb; P{UAS-AUG-DsRed}Ec
|Total=1

REFDSR
{
RDID|FBrf0136779
|Kasuya and Iverson
|2000.11.13
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136779
|Kasuya and Iverson
|2000.11.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018005	ICL 1 P	SYM 1 P{UAS-AUG-DsRed}Ec	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 23 Jul 2001	RESZ 429
ID|FBti0018005
SYM|P{UAS-AUG-DsRed}Ec
ASTP|<fbsym>FBtp0014535==P{UAS-AUG-DsRed}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
SK|FBst0006280
|P{w[+mC]=UAS-AUG-DsRed}Ea, w[*]; P{UAS-AUG-DsRed}Eb; P{UAS-AUG-DsRed}Ec
|Total=1

REFDSR
{
RDID|FBrf0136779
|Kasuya and Iverson
|2000.11.13
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136779
|Kasuya and Iverson
|2000.11.13
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018026	ICL 1 P	SYM 1 P{MTW}B	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 23 Jul 2001	RESZ 259
ID|FBti0018026
SYM|P{MTW}B
SYN|MTW(3)B
ASTP|<fbsym>FBtp0014472==P{MTW}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P

REFDSR
{
RDID|FBrf0137022
|Faucheux et al.
|2001
SYN|MTW(3)B
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137022
|Faucheux et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018030	ICL 1 P	SYM 1 P{MTW}C	ASTR 1 -	CLOC 1 61C9	REF 1 2	DT 1 23 Jul 2001	RESZ 379
ID|FBti0018030
SYM|P{MTW}C
SYN|MTW(3)C
ASTP|<fbsym>FBtp0014472==P{MTW}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
ASGN|<fbsym>FBgn0000575==emc</fbsym>

REFDSR
{
RDID|FBrf0137022
|Faucheux et al.
|2001
SYN|MTW(3)C
CLOC|61C9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000575==emc</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137022
|Faucheux et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018052	ICL 1 P	SYM 1 P{lyB}flam<up>py+P</up>	ASTR 1 -	CLOC 1 20A1--2	REF 1 2	DT 1 23 Jul 2001	RESZ 451
ID|FBti0018052
SYM|P{lyB}flam<up>py+P</up>
ASTP|<fbsym>FBtp0012979==P{lyB}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
ASGN|<fbsym>FBgn0005628==flam</fbsym>

REFDSR
{
RDID|FBrf0136953
|Robert et al.
|2001
SYN|P{lyB}flam<up>py+P</up>
ASAL|<fbsym>FBal0123859==flam<up>py+P</up></fbsym>
CLOC|20A1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005628==flam</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136953
|Robert et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0123859==flam<up>py+P</up></fbsym>

REFDSR
{
RDID|FBrf0136953
|Robert et al.
|2001
PHP|Recessive permissive <fbsym>FBgn0005628==flam</fbsym> allele.
}

REF
{
REFM|FBrf0136953
|Robert et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018056	ICL 1 P	SYM 1 P{MTW}caup<up>L</up>	ASTR 1 -	CLOC 1 69D1	REF 1 2	DT 1 23 Jul 2001	RESZ 464
ID|FBti0018056
SYM|P{MTW}caup<up>L</up>
SYN|MTW(3)L
ASTP|<fbsym>FBtp0014472==P{MTW}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
ASGN|<fbsym>FBgn0015919==caup</fbsym>

REFDSR
{
RDID|FBrf0137022
|Faucheux et al.
|2001
SYN|MTW(3)L
|P{MTW}caup<up>L</up>
ASAL|<fbsym>FBal0123928==caup<up>L</up></fbsym>
CLOC|69D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0015919==caup</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137022
|Faucheux et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018069	ICL 1 P	SYM 1 P{lacZ}kni<up>Schuh</up>	ASTR 1 -	CLOC 1 77E3	REF 1 2	DT 1 23 Jul 2001	RESZ 623
ID|FBti0018069
SYM|P{lacZ}kni<up>Schuh</up>
SYN|kni-lacZ
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|23 Jul 2001
|23 Jul 2001
ICL|P
ASGN|<fbsym>FBgn0001320==kni</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
ASAL|<fbsym>FBal0155142==kni<up>Schuh</up></fbsym>
}

REFDSR
{
RDID|FBrf0135726
|Glazer and Shilo
|2001
SYN|kni-lacZ
|P{lacZ}kni<up>Schuh</up>
ASAL|<fbsym>FBal0124214==Ecol\lacZ<up>kni-Schuh</up></fbsym>
CLOC|77E3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0001320==kni</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0135726
|Glazer and Shilo
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018166	ICL 1 P	SYM 1 P{GawB}scc<up>P</up>	ASTR 1 -	CLOC 1 61C (determined by in situ hybridization)	REF 1 2	DT 1 4 Sep 2001	RESZ 564
ID|FBti0018166
SYM|P{GawB}scc<up>P</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|4 Sep 2001
|4 Sep 2001
ICL|P
ASGN|<fbsym>FBgn0045037==scc</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
SYN|P{GawB}scc<up>P</up>
ASAL|<fbsym>FBal0124951==scc<up>P</up></fbsym>
|<fbsym>FBal0125282==Scer\GAL4<up>scc-P</up></fbsym>
CLOC|61C (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0045037==scc</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0124951==scc<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|Homozygous adults have a cleft in the fan-shaped body and a ventrally
|opened ellipsoid body with intermediate penetrance.
|<fbsym>FBal0124951==scc<up>P</up></fbsym>/<fbsym>FBab0002367==Df(3L)emc-E12</fbsym> flies have no
| mutant adult central brain phenotype.
|Heterozygotes have no adult central brain defect.
PHM|ellipsoid body
|fan-shaped body
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018174	ICL 1 P	SYM 1 P{GawB}fdl<up>P</up>	ASTR 1 -	CLOC 1 49A9--10	REF 1 2	DT 1 4 Sep 2001	RESZ 531
ID|FBti0018174
SYM|P{GawB}fdl<up>P</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|4 Sep 2001
|4 Sep 2001
ICL|P
ASGN|<fbsym>FBgn0045063==fdl</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
SYN|P{GawB}fdl<up>P</up>
ASAL|<fbsym>FBal0125063==fdl<up>P</up></fbsym>
|<fbsym>FBal0125284==Scer\GAL4<up>fdl-P</up></fbsym>
CLOC|49A9--10
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0045063==fdl</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0125063==fdl<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|When originally isolated, homozygous adults showed a central cleft
|in the protocerebral bridge. After 8 generations of outcrossing homozygous
|adults showed a midly penetrant phenotype of &bgr; lobe fusion in the
|central brain.
|<fbsym>FBal0125063==fdl<up>P</up></fbsym>/<fbsym>FBab0002246==Df(2R)vg135</fbsym> adults show fusion
| of the &bgr; lobes at a very
|high frequency.
|Heterozygotes have no adult central brain defect.
PHM|protocerebral bridge
|beta-lobe
|(with Df(2R)vg135) beta-lobe
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018176	ICL 1 P	SYM 1 P{GawB}bwa<up>P</up>	ASTR 1 -	CLOC 1 38B2--3	REF 1 2	DT 1 4 Sep 2001	RESZ 530
ID|FBti0018176
SYM|P{GawB}bwa<up>P</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|4 Sep 2001
|4 Sep 2001
ICL|P
ASGN|<fbsym>FBgn0045064==bwa</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
SYN|P{GawB}bwa<up>P</up>
ASAL|<fbsym>FBal0125102==bwa<up>P</up></fbsym>
|<fbsym>FBal0125286==Scer\GAL4<up>bwa-P</up></fbsym>
CLOC|38B2--3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0045064==bwa</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0125102==bwa<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|When originally isolated, homozygous adults displayed a discrete defect
|in the ellipsoid body. After five generations of outcrossing, homozygous
|adults showed partial or total fusion of left and right &bgr; lobes with
|low frequency.
|<fbsym>FBal0125102==bwa<up>P</up></fbsym>/<fbsym>FBab0001658==Df(2L)TW84</fbsym> adults show fusion of
| the left and right &bgr; and
|&bgr;' lobes with high penetrance.
|Heterozygotes have no adult central brain defect.
PHM|ellipsoid body
|beta-lobe
|(with Df(2L)TW84) beta-lobe
|(with Df(2L)TW84) beta'-lobe
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018177	ICL 1 P	SYM 1 P{GawB}bst<up>P</up>	ASTR 1 -	CLOC 1 36B	REF 1 2	DT 1 4 Sep 2001	RESZ 526
ID|FBti0018177
SYM|P{GawB}bst<up>P</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|4 Sep 2001
|4 Sep 2001
ICL|P
ASGN|<fbsym>FBgn0045065==bst</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
SYN|P{GawB}bst<up>P</up>
ASAL|<fbsym>FBal0125106==bst<up>P</up></fbsym>
|<fbsym>FBal0125287==Scer\GAL4<up>bst-P</up></fbsym>
CLOC|36B
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0045065==bst</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0125106==bst<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|When originally isolated, homozygous adults displayed an ellipsoid
|body opened ventrally with a strong penetrance. This phenotype disappeared
|after a few generations, but outcrossing recovered an ellipsoid body
|defect with weak penetrance, indicating that the phenotype is very
|sensitive to genetic background.
|<fbsym>FBal0125106==bst<up>P</up></fbsym>/<fbsym>FBab0001470==Df(2L)H20</fbsym> or
| <fbsym>FBal0125106==bst<up>P</up></fbsym>/<fbsym>FBab0022223==Df(2L)cact-255rv64</fbsym> adults have a
|ventrally opened ellipsoid body phenotype that is stronger than that
|... (see <fbsym>FBal0125106==bst<up>P</up></fbsym> report)
PHM|ellipsoid body
|(with Df(2L)H20) ellipsoid body
|(with Df(2L)cact-255rv64) ellipsoid body
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018178	ICL 1 P	SYM 1 P{GawB}eas<up>alaP</up>	ASTR 1 -	CLOC 1 14A--B (determined by in situ hybridization)	REF 1 2	DT 1 29 Nov 2005	RESZ 686
ID|FBti0018178
SYM|P{GawB}eas<up>alaP</up>
SYN|P{GawB}ala<up>P</up>
|P{GawB}eas<up>ala-P</up>
|P{GawB}eas<up>alaP</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|29 Nov 2005
|4 Sep 2001
ICL|P
ASGN|<fbsym>FBgn0000536==eas</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>
|<fbsym>FBgn0043963==ala</fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
SYN|P{GawB}ala<up>P</up>
ASAL|<fbsym>FBal0125158==eas<up>alaP</up></fbsym>
|<fbsym>FBal0125292==Scer\GAL4<up>eas-alaP</up></fbsym>
CLOC|14A--B (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0043963==ala</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0122974
|Boquet et al.
|2000
}

ALESR
{
ASYM|<fbsym>FBal0125158==eas<up>alaP</up></fbsym>

REFDSR
{
RDID|FBrf0122974
|Boquet et al.
|2000
PHP|Homozygous flies show fusion of both &bgr; and &bgr;' lobes with intermediate
|frequency and a reduction or absence of the &agr; lobes in the central
|brain.
|<fbsym>eas<up>alaP</up></fbsym>/<fbsym>FBab0022047==Df(1)4b18</fbsym> adults show a very
| high frequency of &bgr; lobe fusion
|in the central brain. &agr; lobes are absent.
|Heterozygotes have no adult central brain defect.
PHM|beta-lobe
|beta'-lobe
|alpha-lobe
|(with Df(1)4b18) beta-lobe
|(with Df(1)4b18) alpha-lobe
}

REFDSR
{
RDID|FBrf0183862
|Pascual et al.
|2005
PHP|<fbsym>eas<up>alaP</up></fbsym> mutants show no bang-sensitive phenotype,
| either as homozygotes
|or as transheterozygotes with <fbsym>FBal0003489==eas<up>2</up></fbsym> or <fbsym>FBab0022047==Df(1)4b18</fbsym>.
|<fbsym>eas<up>alaP</up></fbsym> mutants have a range of defects in the
| mushroom body; 36%
|lack &bgr;' and &bgr; lobes in both hemispheres, 4.5% lack &agr;' and
|&agr; vertical lobes in both hemispheres, while 10.5% possess all five
|lobes in both hemispheres. The remaining flies have different combinations
|of mushroom body phenotype in the left and right hemisphere.
|... (see <fbsym>eas<up>alaP</up></fbsym> report)
PHM|alpha-lobe
|alpha'-lobe
|beta-lobe
|beta'-lobe
|calyx of mushroom body
}

REF
{
REFM|FBrf0122974
|Boquet et al.
|2000
REFM|FBrf0183862
|Pascual et al.
|2005
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0018245	ICL 1 P	SYM 1 P{Winkelried(-FRT)}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 395
ID|FBti0018245
SYM|P{Winkelried(-FRT)}D
ASTP|<fbsym>FBtp0014255==P{Winkelried(-FRT)}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P
PRG|<fbsym>FBti0017779==P{Winkelried}D</fbsym>

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|P{Winkelried(-FRT)}D
ABA|Balancer <fbsym>FBba0000364==In(2)Heidi-P{Winkelried(-FRT)}</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018255	ICL 1 P	SYM 1 P{Winkelried}A	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 261
ID|FBti0018255
SYM|P{Winkelried}A
SYN|Wink-A
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|Wink-A
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018256	ICL 1 P	SYM 1 P{Winkelried}B	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 261
ID|FBti0018256
SYM|P{Winkelried}B
SYN|Wink-B
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|Wink-B
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018257	ICL 1 P	SYM 1 P{Winkelried}C	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 261
ID|FBti0018257
SYM|P{Winkelried}C
SYN|Wink-C
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|Wink-C
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018258	ICL 1 P	SYM 1 P{Winkelried}E	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 261
ID|FBti0018258
SYM|P{Winkelried}E
SYN|Wink-E
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|Wink-E
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018259	ICL 1 P	SYM 1 P{Winkelried}S	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 5 Sep 2001	RESZ 261
ID|FBti0018259
SYM|P{Winkelried}S
SYN|Wink-S
ASTP|<fbsym>FBtp0014564==P{Winkelried}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
SYN|Wink-S
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137374
|Seum et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018341	ICL 1 P	SYM 1 P{UAS-caps.S}Ia	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 5 Sep 2001	RESZ 338
ID|FBti0018341
SYM|P{UAS-caps.S}Ia
SYN|UAS-caps-Ia
ASTP|<fbsym>FBtp0009721==P{UAS-caps.S}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0123213
|Taniguchi et al.
|2000
SYN|UAS-caps-Ia
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0123213
|Taniguchi et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018342	ICL 1 P	SYM 1 P{UAS-caps.S}Ib	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 5 Sep 2001	RESZ 340
ID|FBti0018342
SYM|P{UAS-caps.S}Ib
SYN|UAS-caps-Ib
ASTP|<fbsym>FBtp0009721==P{UAS-caps.S}</fbsym>
DT|5 Sep 2001
|5 Sep 2001
ICL|P

REFDSR
{
RDID|FBrf0123213
|Taniguchi et al.
|2000
SYN|UAS-caps-Ib
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0123213
|Taniguchi et al.
|2000
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018513	ICL 1 P	SYM 1 P{PdL}A	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 15 Oct 2001	RESZ 311
ID|FBti0018513
SYM|P{PdL}A
SYN|PdL(X)A
ASTP|<fbsym>FBtp0014781==P{PdL}</fbsym>
DT|15 Oct 2001
|15 Oct 2001
ICL|P

REFDSR
{
RDID|FBrf0137252
|Landis et al.
|2001
SYN|PdL(X)A
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137252
|Landis et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018690	ICL 1 P	SYM 1 P{}scrib<up>vartul</up>	ASTR 1 -	CLOC 1 97B9--C1	REF 1 2	DT 1 19 Nov 2001	RESZ 523
ID|FBti0018690
SYM|P{}scrib<up>vartul</up>
SYN|P<up>vartul</up>
|p<up>vart</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|19 Nov 2001
|19 Nov 2001
ICL|P
ASGN|<fbsym>FBgn0026178==scrib</fbsym>

REFDSR
{
RDID|FBrf0139743
|Li et al.
|2001
SYN|p<up>vart</up>
|P<up>vartul</up>
|P{}scrib<up>vartul</up>
ASAL|<fbsym>FBal0127185==scrib<up>vartul</up></fbsym>
CLOC|97B9--C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0026178==scrib</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0139743
|Li et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0021017	ICL 1 P	SYM 1 P{wAL}YAL	ASTR 1 -	CLOC 1 18-h25B	REF 1 3	DT 1 19 Jul 2002	RESZ 796
ID|FBti0021017
SYM|P{wAL}YAL
SYN|P[w<up>+</up>]YAL
ASTP|<fbsym>FBtp0015777==P{wAL}</fbsym>
DT|19 Jul 2002
|31 Jan 2002
ICL|P

REFDSR
{
RDID|FBrf0127102
|Haller and Woodruff
|2000
SYN|P[w<up>+</up>]YAL
CLOC|h18-h25B
|Insertion site 
LOCB|in situ
CC|In situ hybridisation indicates that the <fbsym>FBti0021017==P{wAL}YAL</fbsym> insertion maps at or
| near h21-h22 on YS. <fbsym>FBgn0003996==w</fbsym> expression from the <fbsym>FBti0021017==P{wAL}YAL</fbsym> insertion is higher
| when the insertion is inherited from the parental male rather than the
| parental female.
}

REFDSR
{
RDID|FBrf0141794
|Lohe
|2001.11.7
SYN|P{wAL}YAL
CLOC|h18-h25B
|Insertion site 
LOCB|in situ
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0127102
|Haller and Woodruff
|2000
REFM|FBrf0141794
|Lohe
|2001.11.7
}

}

# EOR

TIR
{

RETE|ID 1 FBti0022502	ICL 1 P	SYM 1 P{elavDvORF}edr	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 26 Mar 2002	RESZ 287
ID|FBti0022502
SYM|P{elavDvORF}edr
SYN|elav<up>edr</up>
ASTP|<fbsym>FBtp0005029==P{elavDvORF}</fbsym>
DT|26 Mar 2002
|26 Mar 2002
ICL|P

REFDSR
{
RDID|FBrf0139668
|Lisbin et al.
|2001
SYN|elav<up>edr</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0139668
|Lisbin et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0023617	ICL 1 ?	SYM 1 ?{}SuUR<up>ES</up>	ASTR 1 -	CLOC 1 68A4	REF 1 2	DT 1 18 Jul 2002	RESZ 481
ID|FBti0023617
SYM|?{}SuUR<up>ES</up>
DT|18 Jul 2002
|18 Jul 2002
ICL|?
ASGN|<fbsym>FBgn0025355==SuUR</fbsym>
SK|FBst0004445
|In(1)sc[V2], sc[V2]; <fbsym>FBal0091620==SuUR[ES]</fbsym>
|Total=1

REFDSR
{
RDID|FBrf0147054
|Makunin et al.
|2002
SYN|?{}SuUR<up>ES</up>
ASAL|<fbsym>FBal0091620==SuUR<up>ES</up></fbsym>
CLOC|68A4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0025355==SuUR</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0147054
|Makunin et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0091620==SuUR<up>ES</up></fbsym>

REFDSR
{
RDID|FBrf0102893
|Belyaeva et al.
|1998
PHP|The weak points found in wild-type larval polytene chromosomes are
|missing in all intercalary heterochromatin (IH) regions in homozygous
|larvae. The frequency of ectopic pairing between IH regions and between
|telomeres and pericentric heterochromatin (PH) is greatly decreased.
|Clear bands are seen in regions that form net-like &bgr;-heterochromatin
|in the basements of chromosome arms adjoining the chromocenters in
|wild-type animals. Additional material appears to be present in PH,
|... (see <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> report)
PHM|polytene chromosome weak point
|heterochromatin
|beta-heterochromatin
|alpha-heterochromatin
|intercalary heterochromatin
}

REFDSR
{
RDID|FBrf0104733
|Belyaeva et al.
|1998
PHP|<fbsym>FBal0091620==SuUR<up>ES</up></fbsym> flies lack the "weak" points in the
| intercalary heterochromatin
|of the salivary gland chromosomes, lack ectopic contacts between chromosome
|regions and have additional intercalary heterochromatin in the centromeric
|regions. The intercalary heterochromatin region in 39E does not show
|DNA underreplication. The phenotype is semidominant.
PHM|polytene chromosome weak point
|intercalary heterochromatin
}

REFDSR
{
RDID|FBrf0144771
|Semeshin et al.
|2001
PHP|In <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> mutants new bands appear in the 20BF
| region in polytene
|chromosome squashes. The banding pattern at the base of the chromosome
|2 arms is more clear-cut in <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> mutants. A new
| well structured
|block of chromosome material named "Plato Atlantis", containing a total
|of 25 bands, is formed in the 80C3-81F1-2 interval in
| <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> mutant
|polytene chromosome squashes. The 101E region of chromosome 4 has
|no banding pattern and has the appearance of &agr;-heterochromatin in
|... (see <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> report)
PHM|band
|polytene chromosome
|intercalary heterochromatin
|heterochromatin
}

REFDSR
{
RDID|FBrf0150705
|Volkova and Zhimulev
|2001
PHP|Homozygotes do not show changes in developmental time.
}

REFDSR
{
RDID|FBrf0151235
|Moshkin et al.
|2002
PHP|A number of heterochromatic regions of polytene chromosomes show a
|reproducible banded structure in <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> mutants. The frequency
|of ectopic contacts between pericentric regions decreases in polytene
|chromosomes of <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> mutants.
PHM|heterochromatin
}

REFDSR
{
RDID|FBrf0158793
|Zhimulev et al.
|2003
PHP|The pattern of completion of replication in the polytene chromosomes
|of <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> third instar larvae differs from that of
| Oregon R third
|instar larvae. The <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> larvae have a much lower
| number of late-replicating
|regions than Oregon R larvae. The sets of late-replicating sites in
|<fbsym>FBal0091620==SuUR<up>ES</up></fbsym> and Oregon R are very similar on the whole.
| However, in
|many cases, regions that show typical late replication in Oregon R
|are not labelled in <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> animals. These regions
| include 21D,
|... (see <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> report)
PHM|polytene chromosome
}

REFDSR
{
RDID|FBrf0167627
|Belyaeva et al.
|2003
PHP|Homozygotes show a reduced frequency of heterochromatization in the
|distal parts of the X chromosome of the
| <fbsym>FBab0006121==T(1;2)dor<up>var7</up></fbsym> rearrangement
|compared to animals which are wild-type for <fbsym>FBgn0025355==SuUR</fbsym>.
|Homozygotes show a reduced frequency of heterochromatization in the
|distal parts of the X chromosome of the <fbsym>FBab0003093==Dp(1;1)pn2</fbsym> rearrangement
|compared to animals which are wild-type for <fbsym>FBgn0025355==SuUR</fbsym>.
|XO <fbsym>FBal0091620==SuUR<up>ES</up></fbsym>/+ males show a reduced frequency of heterochromatization
|... (see <fbsym>FBal0091620==SuUR<up>ES</up></fbsym> report)
}

REF
{
REFM|FBrf0102893
|Belyaeva et al.
|1998
REFM|FBrf0104733
|Belyaeva et al.
|1998
REFM|FBrf0144771
|Semeshin et al.
|2001
REFM|FBrf0150705
|Volkova and Zhimulev
|2001
REFM|FBrf0151235
|Moshkin et al.
|2002
REFM|FBrf0158793
|Zhimulev et al.
|2003
REFM|FBrf0167627
|Belyaeva et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0023622	ICL 1 P	SYM 1 P{luc-sniffer}numb<up>nuts</up>	ASTR 1 -	CLOC 1 30B3--5	REF 1 2	DT 1 18 Jul 2002	RESZ 732
ID|FBti0023622
SYM|P{luc-sniffer}numb<up>nuts</up>
SYN|7-32
|7-32A
|7-32
ASTP|<fbsym>FBtp0015729==P{luc-sniffer}</fbsym>
DT|18 Jul 2002
|18 Jul 2002
ICL|P
ASGN|<fbsym>FBgn0002973==numb</fbsym>
|<fbsym>FBgn0014448==Ppyr\LUC</fbsym>

REFDSR
{
RDID|FBrf0144900
|Stempfl et al.
|2002
SYN|7-32
|7-32A
|7-32A
|7-32
|P{luc-sniffer}numb<up>nuts</up>
ASAL|<fbsym>FBal0135657==numb<up>nuts</up></fbsym>
|<fbsym>FBal0135847==Ppyr\LUC<up>numb-nuts</up></fbsym>
CLOC|30B3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002973==numb</fbsym>
PHC|lethal | recessive
|(with numb<up>1</up>) lethal
|(with numb<up>2</up>) lethal
|(with numb<up>3</up>) lethal
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0144900
|Stempfl et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0135657==numb<up>nuts</up></fbsym>

REFDSR
{
RDID|FBrf0144900
|Stempfl et al.
|2002
PHP|91% of heterozygous flies show rhythmic locomotor activity, with a
|period of 24.4 +/- 0.1 hours.
|92% of <fbsym>FBal0135657==numb<up>nuts</up></fbsym>/<fbsym>FBal0082383==numb<up>SW</up></fbsym> flies
| show rhythmic locomotor activity,
|with a period of 24.7 +/- 0.1 hours.
}

REF
{
REFM|FBrf0144900
|Stempfl et al.
|2002
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0023649	ICL 1 P	SYM 1 P{UAS-Snap.P}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 20 Jul 2002	RESZ 339
ID|FBti0023649
SYM|P{UAS-Snap.P}III
SYN|UAS SNAP(III)
ASTP|<fbsym>FBtp0015706==P{UAS-Snap.P}</fbsym>
DT|20 Jul 2002
|19 Jul 2002
ICL|P

REFDSR
{
RDID|FBrf0146969
|Dunne et al.
|2002
SYN|UAS SNAP(III)
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0146969
|Dunne et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0023730	ICL 1 P	SYM 1 P{lacW}exex<up>LacZ</up>	ASTR 1 -	CLOC 1 66A21	REF 1 2	DT 1 27 Aug 2002	RESZ 464
ID|FBti0023730
SYM|P{lacW}exex<up>LacZ</up>
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|27 Aug 2002
|27 Aug 2002
ICL|P
ASGN|<fbsym>FBgn0041156==exex</fbsym>

REFDSR
{
RDID|FBrf0151450
|Broihier and Skeath
|2002
SYN|P{lacW}exex<up>LacZ</up>
ASAL|<fbsym>FBal0137267==exex<up>LacZ</up></fbsym>
CLOC|66A21
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0041156==exex</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0151450
|Broihier and Skeath
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0023759	ICL 1 P	SYM 1 P{GMR-CanB.S}TCAGB	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 27 Aug 2002	RESZ 362
ID|FBti0023759
SYM|P{GMR-CanB.S}TCAGB
ASTP|<fbsym>FBtp0015930==P{GMR-CanB.S}</fbsym>
DT|27 Aug 2002
|27 Aug 2002
ICL|P

REFDSR
{
RDID|FBrf0149012
|Sullivan and Rubin
|2002
SYN|P{GMR-CanB.S}TCAGB
ABA|Balancer <fbsym>FBba0000502==TM3-TCAGB</fbsym>
CH|insertion on balancer | 3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149012
|Sullivan and Rubin
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0023799	ICL 1 H	SYM 1 H{hsp/SP}A	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 28 Aug 2002	RESZ 327
ID|FBti0023799
SYM|H{hsp/SP}A
SYN|H(hsp/SP)A
ASTP|<fbsym>FBtp0015939==H{hsp/SP}</fbsym>
DT|28 Aug 2002
|27 Aug 2002
ICL|H

REFDSR
{
RDID|FBrf0149014
|Simmons et al.
|2002
SYN|H(hsp/SP)A
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149014
|Simmons et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0023800	ICL 1 H	SYM 1 H{hsp/SP}B	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 28 Aug 2002	RESZ 326
ID|FBti0023800
SYM|H{hsp/SP}B
SYN|H(hsp/SP)B
ASTP|<fbsym>FBtp0015939==H{hsp/SP}</fbsym>
DT|28 Aug 2002
|27 Aug 2002
ICL|H

REFDSR
{
RDID|FBrf0149014
|Simmons et al.
|2002
SYN|H(hsp/SP)B
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0149014
|Simmons et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0024288	ICL 1 P	SYM 1 P{hsw<up>a</up>}sd<up>wa</up>	ASTR 1 -	CLOC 1 13F1--4	REF 1 2	DT 1 3 Apr 2003	RESZ 461
ID|FBti0024288
SYM|P{hsw<up>a</up>}sd<up>wa</up>
ASTP|<fbsym>FBtp0003826==P{hsw<up>a</up>}</fbsym>
DT|3 Apr 2003
|3 Apr 2003
ICL|P
ASGN|<fbsym>FBgn0003345==sd</fbsym>

REFDSR
{
RDID|FBrf0155463
|Adams et al.
|2003
SYN|P{hsw<up>a</up>}sd<up>wa</up>
ASAL|<fbsym>FBal0140941==sd<up>wa</up></fbsym>
CLOC|13F1--4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003345==sd</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155463
|Adams et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0025355	ICL 1 P	SYM 1 P{}sn<up>w</up>a	ASTR 1 -	CLOC 1 7D1--2	REF 1 13	DT 1 7 Jul 2003	RESZ 1179
ID|FBti0025355
SYM|P{}sn<up>w</up>a
SYN|P{}P{}sn<up>w</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ID2|FBti0014672
ASGN|<fbsym>FBgn0003447==sn</fbsym>
SK|FBst0002541
|sn[w]; ry[506]
|FBst0003001
|y[1] sn[w]; bw[1]; st[1]
|Total=2

REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
SYN|P{}sn<up>w</up>a
ASAL|<fbsym>FBal0015885==sn<up>w</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0003055==P-element</fbsym> insertions associated with this allele; see <fbsym>FBti0025356==P{}sn<up>w</up>b</fbsym>.
}

REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0049839
|Brookfield and Lewis
|1989
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051102
|Rio
|1990
REFM|FBrf0051965
|Rasmusson et al.
|1990
REFM|FBrf0051968
|Simmons et al.
|1990
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0089801
|Ronsseray et al.
|1996
REFM|FBrf0100571
|Henderson and Glover
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109352
|Biryukova et al.
|1999
REFM|FBrf0149013
|Simmons et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0015885==sn<up>w</up></fbsym>

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Phenotype is unaffected by <fbsym>FBal0032166==mod(mdg4)<up>ul</up></fbsym>.
}

REFDSR
{
RDID|FBrf0051102
|Rio
|1990
PHP|Can mutate during a dysgenic cross to either wild type phenotype or
|a more extreme (<fbsym>FBal0015855==sn<up>e</up></fbsym>) bristle phenotype depending on
| which one of
|the P-elements excises.
}

REFDSR
{
RDID|FBrf0051364
|Misra and Rio
|1990
PHP|The presence of <fbsym>FBal0033899==P\T<up>66</up></fbsym> causes a drastic reduction in destabilization
|of <fbsym>FBal0015885==sn<up>w</up></fbsym> to <fbsym>FBal0015855==sn<up>e</up></fbsym> or
| <fbsym>FBal0015769==sn<up>(+)</up></fbsym>. This repression is not increased
|by <fbsym>FBal0033939==P\T<up>66D1.hs</up></fbsym>, but it is increased by <fbsym>FBal0033938==P\T<up>66C2.hs</up></fbsym>.
}

REFDSR
{
RDID|FBrf0065495
|Misra et al.
|1993
PHP|Repression potential of a <fbsym>FBgn0003055==P-element</fbsym> repressor protein in a singed
|sterility assay of <fbsym>FBal0015885==sn<up>w</up></fbsym>/<fbsym>FBal0015886==sn<up>X2</up></fbsym>
| heterozygotes shows partial correspondence
|with gonadal dysgenic sterility in that strong repression of gonadal
|dysgenic sterility shows some effect in the singed sterility assay.
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Weak singed phenotype, probably class 2. Highly mutable in dysgenic
|genotypes; 40% to 60% of offspring are either normal
| (<fbsym>FBal0015769==sn<up>(+)</up></fbsym>) or
|extreme singed (<fbsym>FBal0015855==sn<up>e</up></fbsym>) in phenotype. These derivatives
| are in turn
|mutable, but at much lower levels. Completely stable in non-dysgenic
|genotypes. Gnarled macrochaetae and kinky microchaetae.
PHM|macrochaeta
|microchaeta
}

REFDSR
{
RDID|FBrf0085576
|Merriman et al.
|1995
PHP|Bristle phenotype is suppressed by <fbsym>FBal0016414==su(s)<up>71</up></fbsym>, and
| partly suppressed
|by <fbsym>FBal0050588==su(s)<up>sn-w:R</up></fbsym>.
}

REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051102
|Rio
|1990
REFM|FBrf0051364
|Misra and Rio
|1990
REFM|FBrf0065495
|Misra et al.
|1993
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0085576
|Merriman et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025356	ICL 1 P	SYM 1 P{}sn<up>w</up>b	ASTR 1 -	CLOC 1 7D1--2	REF 1 13	DT 1 7 Jul 2003	RESZ 1179
ID|FBti0025356
SYM|P{}sn<up>w</up>b
SYN|P{}P{}sn<up>w</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ID2|FBti0014672
ASGN|<fbsym>FBgn0003447==sn</fbsym>
SK|FBst0002541
|sn[w]; ry[506]
|FBst0003001
|y[1] sn[w]; bw[1]; st[1]
|Total=2

REFDSR
{
RDID|FBrf0048245
|Roiha et al.
|1988
SYN|P{}sn<up>w</up>b
ASAL|<fbsym>FBal0015885==sn<up>w</up></fbsym>
CLOC|7D1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003447==sn</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0003055==P-element</fbsym> insertions associated with this allele; see <fbsym>FBti0025355==P{}sn<up>w</up>a</fbsym>.
}

REF
{
REFM|FBrf0048245
|Roiha et al.
|1988
REFM|FBrf0049839
|Brookfield and Lewis
|1989
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051102
|Rio
|1990
REFM|FBrf0051965
|Rasmusson et al.
|1990
REFM|FBrf0051968
|Simmons et al.
|1990
REFM|FBrf0063381
|Collins et al.
|1983
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0089801
|Ronsseray et al.
|1996
REFM|FBrf0100571
|Henderson and Glover
|1998
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109352
|Biryukova et al.
|1999
REFM|FBrf0149013
|Simmons et al.
|2002
}

ALESR
{
ASYM|<fbsym>FBal0015885==sn<up>w</up></fbsym>

REFDSR
{
RDID|FBrf0050555
|Georgiev and Gerasimova
|1989
PHP|Phenotype is unaffected by <fbsym>FBal0032166==mod(mdg4)<up>ul</up></fbsym>.
}

REFDSR
{
RDID|FBrf0051102
|Rio
|1990
PHP|Can mutate during a dysgenic cross to either wild type phenotype or
|a more extreme (<fbsym>FBal0015855==sn<up>e</up></fbsym>) bristle phenotype depending on
| which one of
|the P-elements excises.
}

REFDSR
{
RDID|FBrf0051364
|Misra and Rio
|1990
PHP|The presence of <fbsym>FBal0033899==P\T<up>66</up></fbsym> causes a drastic reduction in destabilization
|of <fbsym>FBal0015885==sn<up>w</up></fbsym> to <fbsym>FBal0015855==sn<up>e</up></fbsym> or
| <fbsym>FBal0015769==sn<up>(+)</up></fbsym>. This repression is not increased
|by <fbsym>FBal0033939==P\T<up>66D1.hs</up></fbsym>, but it is increased by <fbsym>FBal0033938==P\T<up>66C2.hs</up></fbsym>.
}

REFDSR
{
RDID|FBrf0065495
|Misra et al.
|1993
PHP|Repression potential of a <fbsym>FBgn0003055==P-element</fbsym> repressor protein in a singed
|sterility assay of <fbsym>FBal0015885==sn<up>w</up></fbsym>/<fbsym>FBal0015886==sn<up>X2</up></fbsym>
| heterozygotes shows partial correspondence
|with gonadal dysgenic sterility in that strong repression of gonadal
|dysgenic sterility shows some effect in the singed sterility assay.
}

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
PHP|Weak singed phenotype, probably class 2. Highly mutable in dysgenic
|genotypes; 40% to 60% of offspring are either normal
| (<fbsym>FBal0015769==sn<up>(+)</up></fbsym>) or
|extreme singed (<fbsym>FBal0015855==sn<up>e</up></fbsym>) in phenotype. These derivatives
| are in turn
|mutable, but at much lower levels. Completely stable in non-dysgenic
|genotypes. Gnarled macrochaetae and kinky microchaetae.
PHM|macrochaeta
|microchaeta
}

REFDSR
{
RDID|FBrf0085576
|Merriman et al.
|1995
PHP|Bristle phenotype is suppressed by <fbsym>FBal0016414==su(s)<up>71</up></fbsym>, and
| partly suppressed
|by <fbsym>FBal0050588==su(s)<up>sn-w:R</up></fbsym>.
}

REF
{
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051102
|Rio
|1990
REFM|FBrf0051364
|Misra and Rio
|1990
REFM|FBrf0065495
|Misra et al.
|1993
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0085576
|Merriman et al.
|1995
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025360	ICL 1 ?	SYM 1 ?{}vg<up>TP</up>b	ASTR 1 -	CLOC 1 49E1	REF 1 3	DT 1 7 Jul 2003	RESZ 618
ID|FBti0025360
SYM|?{}vg<up>TP</up>b
SYN|412{}?{}vg<up>TP</up>
DT|7 Jul 2003
|7 Jul 2003
ICL|?
ID2|FBti0014754
ASGN|<fbsym>FBgn0003975==vg</fbsym>

REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
SYN|?{}vg<up>TP</up>b
ASAL|<fbsym>FBal0035915==vg<up>TP</up></fbsym>
CLOC|49E1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003975==vg</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see <fbsym>FBti0025359==412{}vg<up>TP</up>a</fbsym>.
}

REF
{
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0099521
|Silber et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0035915==vg<up>TP</up></fbsym>

REFDSR
{
RDID|FBrf0064705
|Silber et al.
|1993
PHP|Homozygotes display highly resistance to aminopterin.
}

REFDSR
{
RDID|FBrf0099521
|Silber et al.
|1997
PHP|Wing length increases with increasing temperature.
PHM|wing | conditional cs
}

REF
{
REFM|FBrf0064705
|Silber et al.
|1993
REFM|FBrf0099521
|Silber et al.
|1997
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025361	ICL 1 FB	SYM 1 FB{}w<up>c</up>a	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 7 Jul 2003	RESZ 630
ID|FBti0025361
SYM|FB{}w<up>c</up>a
SYN|FB{}NOF{}w<up>c</up>
ASTP|<fbsym>FBtp0011426==FB</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|FB
ID2|FBti0014792
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0051943
|Harden and Ashburner
|1990
SYN|FB{}w<up>c</up>a
ASAL|<fbsym>FBal0018221==w<up>c</up></fbsym>
MU|X ray
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see <fbsym>FBti0025362==NOF{}w<up>c</up>b</fbsym>.
}

REF
{
REFM|FBrf0051943
|Harden and Ashburner
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018221==w<up>c</up></fbsym>

REFDSR
{
RDID|FBrf0037621
|Collins and Rubin
|1982
PHP|Eye color: light reddish-orange.
}

REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: crimson.
PHM|pigment cell
}

REF
{
REFM|FBrf0037621
|Collins and Rubin
|1982
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025362	ICL 1 NOF	SYM 1 NOF{}w<up>c</up>b	ASTR 1 -	CLOC 1 3B6	REF 1 2	DT 1 7 Jul 2003	RESZ 633
ID|FBti0025362
SYM|NOF{}w<up>c</up>b
SYN|FB{}NOF{}w<up>c</up>
ASTP|<fbsym>FBtp0011454==NOF</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|NOF
ID2|FBti0014792
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0051943
|Harden and Ashburner
|1990
SYN|NOF{}w<up>c</up>b
ASAL|<fbsym>FBal0018221==w<up>c</up></fbsym>
MU|X ray
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see <fbsym>FBti0025361==FB{}w<up>c</up>a</fbsym>.
}

REF
{
REFM|FBrf0051943
|Harden and Ashburner
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018221==w<up>c</up></fbsym>

REFDSR
{
RDID|FBrf0037621
|Collins and Rubin
|1982
PHP|Eye color: light reddish-orange.
}

REFDSR
{
RDID|FBrf0094159
|Bhadra et al.
|1997
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: crimson.
PHM|pigment cell
}

REF
{
REFM|FBrf0037621
|Collins and Rubin
|1982
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025363	ICL 1 P	SYM 1 P{}y<up>+ns</up>a	ASTR 1 -	CLOC 1 1A5	REF 1 3	DT 1 7 Jul 2003	RESZ 698
ID|FBti0025363
SYM|P{}y<up>+ns</up>a
SYN|P{}P{}y<up>+ns</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ID2|FBti0014812
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
SYN|P{}y<up>+ns</up>a
ASAL|<fbsym>FBal0033195==y<up>+ns</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0003055==P-element</fbsym> insertions associated with this allele; see <fbsym>FBti0025364==P{}y<up>+ns</up>b</fbsym>.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108187
|Golovnin et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0033195==y<up>+ns</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
PHP|Body color: body and wing wild-type; leg and thorax bristles reduced pigmentation.
PHM|macrochaeta & adult thorax
|macrochaeta & leg
}

REFDSR
{
RDID|FBrf0108187
|Golovnin et al.
|1999
PHP|Body color: flies have wild-type pigmentation of the body and wings.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0108187
|Golovnin et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025364	ICL 1 P	SYM 1 P{}y<up>+ns</up>b	ASTR 1 -	CLOC 1 1A5	REF 1 3	DT 1 7 Jul 2003	RESZ 698
ID|FBti0025364
SYM|P{}y<up>+ns</up>b
SYN|P{}P{}y<up>+ns</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ID2|FBti0014812
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
SYN|P{}y<up>+ns</up>b
ASAL|<fbsym>FBal0033195==y<up>+ns</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0003055==P-element</fbsym> insertions associated with this allele; see <fbsym>FBti0025363==P{}y<up>+ns</up>a</fbsym>.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0108187
|Golovnin et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0033195==y<up>+ns</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
PHP|Body color: body and wing wild-type; leg and thorax bristles reduced pigmentation.
PHM|macrochaeta & adult thorax
|macrochaeta & leg
}

REFDSR
{
RDID|FBrf0108187
|Golovnin et al.
|1999
PHP|Body color: flies have wild-type pigmentation of the body and wings.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0108187
|Golovnin et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025393	ICL 1 P	SYM 1 P{}y<up>+s</up>a	ASTR 1 -	CLOC 1 1A5	REF 1 3	DT 1 7 Jul 2003	RESZ 1006
ID|FBti0025393
SYM|P{}y<up>+s</up>a
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
PRG|<fbsym>FBti0002420==gypsy{}y<up>2</up></fbsym>
ASGN|<fbsym>FBgn0004034==y</fbsym>
ABA|<fbsym>FBab0028817==Tp(1;1)y<up>+s</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
SYN|P{}y<up>+s</up>a
ASAL|<fbsym>FBal0062346==y<up>+s</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of 3 insertions associated with this allele; see
| <fbsym>FBti0025394==P{}y<up>+s</up>b</fbsym> and <fbsym>FBti0002420==gypsy{}y<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
ASAL|<fbsym>FBal0098590==y<up>+s27</up></fbsym>
|<fbsym>FBal0098589==y<up>+s32</up></fbsym>
|<fbsym>FBal0098588==y<up>+sA11</up></fbsym>
|<fbsym>FBal0098587==y<up>+sA12</up></fbsym>
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109352
|Biryukova et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0098587==y<up>+sA12</up></fbsym>

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: flies have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0098588==y<up>+sA11</up></fbsym>

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0062346==y<up>+s</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
PHP|Pigmentation of all cuticular structures is normal in hemizygous males.
|This phenotype is not altered by either <fbsym>FBal0032166==mod(mdg4)<up>ul</up></fbsym>
| or <fbsym>FBal0016319==su(Hw)<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: homozygotes have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0098589==y<up>+s32</up></fbsym>

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: flies have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0098590==y<up>+s27</up></fbsym>

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025394	ICL 1 P	SYM 1 P{}y<up>+s</up>b	ASTR 1 -	CLOC 1 1A5	REF 1 3	DT 1 7 Jul 2003	RESZ 962
ID|FBti0025394
SYM|P{}y<up>+s</up>b
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
PRG|<fbsym>FBti0002420==gypsy{}y<up>2</up></fbsym>
ASGN|<fbsym>FBgn0004034==y</fbsym>
ABA|<fbsym>FBab0028817==Tp(1;1)y<up>+s</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
SYN|P{}y<up>+s</up>b
ASAL|<fbsym>FBal0062346==y<up>+s</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of 3 insertions associated with this allele; see
| <fbsym>FBti0025393==P{}y<up>+s</up>a</fbsym> and <fbsym>FBti0002420==gypsy{}y<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
ASAL|<fbsym>FBal0098590==y<up>+s27</up></fbsym>
|<fbsym>FBal0098588==y<up>+sA11</up></fbsym>
|<fbsym>FBal0098587==y<up>+sA12</up></fbsym>
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0109352
|Biryukova et al.
|1999
}

ALESR
{
ASYM|<fbsym>FBal0098587==y<up>+sA12</up></fbsym>

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: flies have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0098588==y<up>+sA11</up></fbsym>

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0062346==y<up>+s</up></fbsym>

REFDSR
{
RDID|FBrf0093460
|Georgiev et al.
|1997
PHP|Pigmentation of all cuticular structures is normal in hemizygous males.
|This phenotype is not altered by either <fbsym>FBal0032166==mod(mdg4)<up>ul</up></fbsym>
| or <fbsym>FBal0016319==su(Hw)<up>2</up></fbsym>.
}

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: homozygotes have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0093460
|Georgiev et al.
|1997
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

ALESR
{
ASYM|<fbsym>FBal0098590==y<up>+s27</up></fbsym>

REFDSR
{
RDID|FBrf0109352
|Biryukova et al.
|1999
PHP|Body color: flies have wild-type pigmentation in the body cuticle
|and wing blade and in the thoracic, leg, wing and abdominal bristles.
}

REF
{
REFM|FBrf0109352
|Biryukova et al.
|1999
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0025448	ICL 1 gypsy	SYM 1 gypsy{}ovo<up>yct</up>a	ASTR 1 -	CLOC 1 4E2	REF 1 2	DT 1 7 Jul 2003	RESZ 678
ID|FBti0025448
SYM|gypsy{}ovo<up>yct</up>a
SYN|gypsy{}gypsy{}ovo<up>yct</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|gypsy
ID2|FBti0015219
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0104424
|Dej et al.
|1998
SYN|gypsy{}ovo<up>yct</up>a
ASAL|<fbsym>FBal0092557==ovo<up>yct</up></fbsym>
CLOC|4E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003028==ovo</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0001167==gypsy</fbsym> insertions associated with this allele; see <fbsym>FBti0025449==gypsy{}ovo<up>yct</up>b</fbsym>.
}

REF
{
REFM|FBrf0104424
|Dej et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0025449	ICL 1 gypsy	SYM 1 gypsy{}ovo<up>yct</up>b	ASTR 1 -	CLOC 1 4E2	REF 1 2	DT 1 7 Jul 2003	RESZ 678
ID|FBti0025449
SYM|gypsy{}ovo<up>yct</up>b
SYN|gypsy{}gypsy{}ovo<up>yct</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|gypsy
ID2|FBti0015219
ASGN|<fbsym>FBgn0003028==ovo</fbsym>

REFDSR
{
RDID|FBrf0104424
|Dej et al.
|1998
SYN|gypsy{}ovo<up>yct</up>b
ASAL|<fbsym>FBal0092557==ovo<up>yct</up></fbsym>
CLOC|4E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003028==ovo</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two <fbsym>FBgn0001167==gypsy</fbsym> insertions associated with this allele; see <fbsym>FBti0025448==gypsy{}ovo<up>yct</up>a</fbsym>.
}

REF
{
REFM|FBrf0104424
|Dej et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0025566	ICL 1 P	SYM 1 P{GS}th<up>EP.M</up>	ASTR 1 -	CLOC 1 72D1	REF 1 2	DT 1 7 Jul 2003	RESZ 458
ID|FBti0025566
SYM|P{GS}th<up>EP.M</up>
SYN|UAS-DIAP1
ASTP|<fbsym>FBtp0011344==P{GS}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0003691==th</fbsym>

REFDSR
{
RDID|FBrf0151836
|Moreno et al.
|2002
SYN|P{GS}th<up>EP.M</up>
|UAS-DIAP1
ASAL|<fbsym>FBal0143164==th<up>EP.M</up></fbsym>
CLOC|72D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003691==th</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0151836
|Moreno et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026479	ICL 1 P	SYM 1 P{lacZ}E(sda)O<up>O</up>	ASTR 1 -	CLOC 1 41C (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026479
SYM|P{lacZ}E(sda)O<up>O</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066120==E(sda)O</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)O<up>O</up>
ASAL|<fbsym>FBal0144990==E(sda)O<up>O</up></fbsym>
CLOC|41C (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066120==E(sda)O</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144990==E(sda)O<up>O</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|10% of homozygotes have a bang sensitive phenotype.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026481	ICL 1 P	SYM 1 P{lacZ}E(sda)M<up>M</up>	ASTR 1 -	CLOC 1 75C (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026481
SYM|P{lacZ}E(sda)M<up>M</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066122==E(sda)M</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)M<up>M</up>
ASAL|<fbsym>FBal0144992==E(sda)M<up>M</up></fbsym>
CLOC|75C (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066122==E(sda)M</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144992==E(sda)M<up>M</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|Homozygotes are not bang sensitive.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026482	ICL 1 P	SYM 1 P{lacZ}E(sda)L<up>L</up>	ASTR 1 -	CLOC 1 86D (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026482
SYM|P{lacZ}E(sda)L<up>L</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066123==E(sda)L</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)L<up>L</up>
ASAL|<fbsym>FBal0144993==E(sda)L<up>L</up></fbsym>
CLOC|86D (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066123==E(sda)L</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144993==E(sda)L<up>L</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|Homozygotes are not bang sensitive.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026483	ICL 1 P	SYM 1 P{lacZ}E(sda)J<up>J</up>	ASTR 1 -	CLOC 1 88A (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026483
SYM|P{lacZ}E(sda)J<up>J</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066124==E(sda)J</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)J<up>J</up>
ASAL|<fbsym>FBal0144994==E(sda)J<up>J</up></fbsym>
CLOC|88A (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066124==E(sda)J</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144994==E(sda)J<up>J</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|60% of homozygotes have a bang sensitive phenotype.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026484	ICL 1 P	SYM 1 P{lacZ}E(sda)I<up>I</up>	ASTR 1 -	CLOC 1 61D (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 475
ID|FBti0026484
SYM|P{lacZ}E(sda)I<up>I</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066125==E(sda)I</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)I<up>I</up>
ASAL|<fbsym>FBal0144995==E(sda)I<up>I</up></fbsym>
CLOC|61D (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066125==E(sda)I</fbsym>
PHC|lethal | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026485	ICL 1 P	SYM 1 P{lacZ}E(sda)H<up>H</up>	ASTR 1 -	CLOC 1 68F1	REF 1 2	DT 1 7 Jul 2003	RESZ 469
ID|FBti0026485
SYM|P{lacZ}E(sda)H<up>H</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066126==E(sda)H</fbsym>
|<fbsym>FBgn0041096==rols</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)H<up>H</up>
ASAL|<fbsym>FBal0144996==E(sda)H<up>H</up></fbsym>
CLOC|68F1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0041096==rols</fbsym>
PHC|lethal | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026486	ICL 1 P	SYM 1 P{lacZ}E(sda)G<up>G</up>	ASTR 1 -	CLOC 1 89B (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 475
ID|FBti0026486
SYM|P{lacZ}E(sda)G<up>G</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066127==E(sda)G</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)G<up>G</up>
ASAL|<fbsym>FBal0144997==E(sda)G<up>G</up></fbsym>
CLOC|89B (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066127==E(sda)G</fbsym>
PHC|lethal | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026487	ICL 1 P	SYM 1 P{lacZ}E(sda)F<up>F</up>	ASTR 1 -	CLOC 1 47F (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026487
SYM|P{lacZ}E(sda)F<up>F</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066128==E(sda)F</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)F<up>F</up>
ASAL|<fbsym>FBal0144998==E(sda)F<up>F</up></fbsym>
CLOC|47F (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066128==E(sda)F</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144998==E(sda)F<up>F</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|33% of homozygotes have a bang sensitive phenotype.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026488	ICL 1 P	SYM 1 P{lacZ}E(sda)D<up>D</up>	ASTR 1 -	CLOC 1 59A (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026488
SYM|P{lacZ}E(sda)D<up>D</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066129==E(sda)D</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)D<up>D</up>
ASAL|<fbsym>FBal0144999==E(sda)D<up>D</up></fbsym>
CLOC|59A (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066129==E(sda)D</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0144999==E(sda)D<up>D</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|84% of homozygotes show a bang sensitive phenotype.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026489	ICL 1 P	SYM 1 P{lacZ}E(sda)C<up>C</up>	ASTR 1 -	CLOC 1 51F9 (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 453
ID|FBti0026489
SYM|P{lacZ}E(sda)C<up>C</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066130==E(sda)C</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)C<up>C</up>
ASAL|<fbsym>FBal0145000==E(sda)C<up>C</up></fbsym>
CLOC|51F9 (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066130==E(sda)C</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0145000==E(sda)C<up>C</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|Homozygotes are not bang sensitive.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026490	ICL 1 P	SYM 1 P{lacZ}E(sda)B<up>B</up>	ASTR 1 -	CLOC 1 85D (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026490
SYM|P{lacZ}E(sda)B<up>B</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066131==E(sda)B</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)B<up>B</up>
ASAL|<fbsym>FBal0145001==E(sda)B<up>B</up></fbsym>
CLOC|85D (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066131==E(sda)B</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0145001==E(sda)B<up>B</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|Homozygotes are not bang sensitive.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026491	ICL 1 P	SYM 1 P{lacZ}E(sda)A<up>A</up>	ASTR 1 -	CLOC 1 86B (determined by in situ hybridization)	REF 1 2	DT 1 7 Jul 2003	RESZ 452
ID|FBti0026491
SYM|P{lacZ}E(sda)A<up>A</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|7 Jul 2003
|7 Jul 2003
ICL|P
ASGN|<fbsym>FBgn0066132==E(sda)A</fbsym>

REFDSR
{
RDID|FBrf0155803 
SYN|P{lacZ}E(sda)A<up>A</up>
ASAL|<fbsym>FBal0145002==E(sda)A<up>A</up></fbsym>
CLOC|86B (determined by in situ hybridization)
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0066132==E(sda)A</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155803 
}

ALESR
{
ASYM|<fbsym>FBal0145002==E(sda)A<up>A</up></fbsym>

REFDSR
{
RDID|FBrf0155803 
PHP|100% of homozygotes show a bang sensitive phenotype.
}

REF
{
REFM|FBrf0155803 
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0026627	ICL 1 P	SYM 1 P{UAS-disco.M}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 8 Jul 2003	RESZ 425
ID|FBti0026627
SYM|P{UAS-disco.M}II
SYN|UAS-disco<up>M</up>II
ASTP|<fbsym>FBtp0016287==P{UAS-disco.M}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P
SK|FBst0006846
|y[1] w[*]; P{w[+mC]=UAS-disco.M}II/CyO
|Total=1

REFDSR
{
RDID|FBrf0152356
|Robertson et al.
|2002
SYN|UAS-disco<up>M</up>II
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152356
|Robertson et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026628	ICL 1 P	SYM 1 P{UAS-disco.M}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 8 Jul 2003	RESZ 376
ID|FBti0026628
SYM|P{UAS-disco.M}III
SYN|UAS-disco<up>M</up>III
ASTP|<fbsym>FBtp0016287==P{UAS-disco.M}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152356
|Robertson et al.
|2002
SYN|UAS-disco<up>M</up>III
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152356
|Robertson et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026629	ICL 1 P	SYM 1 P{UAS-disco.C}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 8 Jul 2003	RESZ 376
ID|FBti0026629
SYM|P{UAS-disco.C}III
SYN|UAS-disco<up>C</up>III
ASTP|<fbsym>FBtp0016289==P{UAS-disco.C}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152356
|Robertson et al.
|2002
SYN|UAS-disco<up>C</up>III
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152356
|Robertson et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026632	ICL 1 P	SYM 1 P{UAS-Tor.WT}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 8 Jul 2003	RESZ 399
ID|FBti0026632
SYM|P{UAS-Tor.WT}II
SYN|P[w+]UAS-dTOR<up>WT</up><down>II</down>
ASTP|<fbsym>FBtp0016359==P{UAS-Tor.WT}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>WT</up><down>II</down>
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026633	ICL 1 P	SYM 1 P{UAS-Tor.WT}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 8 Jul 2003	RESZ 483
ID|FBti0026633
SYM|P{UAS-Tor.WT}III
SYN|P[w+]UAS-dTOR<up>WT</up><down>III</down>
ASTP|<fbsym>FBtp0016359==P{UAS-Tor.WT}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P
SK|FBst0007012
|y[1] w[*] P{ry[+t7.2]=hsFLP}1; P{w[+mC]=UAS-Tor.WT}III
|Total=1

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>WT</up><down>III</down>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026634	ICL 1 P	SYM 1 P{UAS-Tor.FRB}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 8 Jul 2003	RESZ 407
ID|FBti0026634
SYM|P{UAS-Tor.FRB}III
SYN|P[w+]UAS-dTOR<up>FRB</up><down>III</down>
ASTP|<fbsym>FBtp0016361==P{UAS-Tor.FRB}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>FRB</up><down>III</down>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026635	ICL 1 P	SYM 1 P{UAS-Tor.FRB}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 8 Jul 2003	RESZ 403
ID|FBti0026635
SYM|P{UAS-Tor.FRB}II
SYN|P[w+]UAS-dTOR<up>FRB</up><down>II</down>
ASTP|<fbsym>FBtp0016361==P{UAS-Tor.FRB}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>FRB</up><down>II</down>
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026636	ICL 1 P	SYM 1 P{UAS-Tor.TED}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 8 Jul 2003	RESZ 463
ID|FBti0026636
SYM|P{UAS-Tor.TED}II
SYN|P[w+]UAS-dTOR<up>TED</up><down>II</down>
ASTP|<fbsym>FBtp0016360==P{UAS-Tor.TED}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P
SK|FBst0007013
|y[1] w[*]; P{w[+mC]=UAS-Tor.TED}II
|Total=1

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>TED</up><down>II</down>
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026637	ICL 1 P	SYM 1 P{UAS-Tor.TED}I	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 8 Jul 2003	RESZ 399
ID|FBti0026637
SYM|P{UAS-Tor.TED}I
SYN|P[w+]UAS-dTOR<up>TED</up><down>I</down>
ASTP|<fbsym>FBtp0016360==P{UAS-Tor.TED}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0152357
|Hennig and Neufeld
|2002
SYN|P[w+]UAS-dTOR<up>TED</up><down>I</down>
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0152357
|Hennig and Neufeld
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026874	ICL 1 P	SYM 1 P{SUPor-P}ROMA	ASTR 1 -	CLOC 1 12	REF 1 2	DT 1 8 Jul 2003	RESZ 305
ID|FBti0026874
SYM|P{SUPor-P}ROMA
SYN|ROMA
ASTP|<fbsym>FBtp0001587==P{SUPor-P}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0155500
|Maggert and Golic
|2002
SYN|ROMA
CLOC|h12
|Insertion site 
LOCB|in situ
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155500
|Maggert and Golic
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026995	ICL 1 P	SYM 1 P{UAS-eiger.M}Av	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 388
ID|FBti0026995
SYM|P{UAS-eiger.M}Av
SYN|UAS-eig
ASTP|<fbsym>FBtp0016697==P{UAS-eiger.M}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0151836
|Moreno et al.
|2002
SYN|UAS-eig
CC|<fbsym>FBtp0016697==P{UAS-eiger.M}</fbsym> insertion with average levels of activity compared to other insertions.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0151836
|Moreno et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0026996	ICL 1 P	SYM 1 P{UAS-eiger.M}weak	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 370
ID|FBti0026996
SYM|P{UAS-eiger.M}weak
ASTP|<fbsym>FBtp0016697==P{UAS-eiger.M}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0151836
|Moreno et al.
|2002
CC|<fbsym>FBtp0016697==P{UAS-eiger.M}</fbsym> insertion with weaker than average activity compared to
| other insertions.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0151836
|Moreno et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027000	ICL 1 P	SYM 1 P{UAS-Btau\msrA.EGFP}B	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 355
ID|FBti0027000
SYM|P{UAS-Btau\msrA.EGFP}B
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)B
|MSRA<up>B</up>
ASTP|<fbsym>FBtp0016966==P{UAS-Btau\msrA.EGFP}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0145202
|Ruan et al.
|2002
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)B
|MSRA<up>B</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145202
|Ruan et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027001	ICL 1 P	SYM 1 P{UAS-Btau\msrA.EGFP}C	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 355
ID|FBti0027001
SYM|P{UAS-Btau\msrA.EGFP}C
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)C
|MSRA<up>C</up>
ASTP|<fbsym>FBtp0016966==P{UAS-Btau\msrA.EGFP}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0145202
|Ruan et al.
|2002
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)C
|MSRA<up>C</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145202
|Ruan et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027002	ICL 1 P	SYM 1 P{UAS-Btau\msrA.EGFP}D	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 355
ID|FBti0027002
SYM|P{UAS-Btau\msrA.EGFP}D
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)D
|MSRA<up>D</up>
ASTP|<fbsym>FBtp0016966==P{UAS-Btau\msrA.EGFP}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0145202
|Ruan et al.
|2002
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)D
|MSRA<up>D</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145202
|Ruan et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027003	ICL 1 P	SYM 1 P{UAS-Btau\msrA.EGFP}E	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 8 Jul 2003	RESZ 355
ID|FBti0027003
SYM|P{UAS-Btau\msrA.EGFP}E
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)E
|MSRA<up>E</up>
ASTP|<fbsym>FBtp0016966==P{UAS-Btau\msrA.EGFP}</fbsym>
DT|8 Jul 2003
|8 Jul 2003
ICL|P

REFDSR
{
RDID|FBrf0145202
|Ruan et al.
|2002
SYN|P(w+mC
|= UAS-AUG-EGFP-MSRA)E
|MSRA<up>E</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0145202
|Ruan et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027408	ICL 1 flea	SYM 1 flea{}Dat<up>lo</up>a	ASTR 1 -	CLOC 1 60B12--C1	REF 1 2	DT 1 1 Mar 2004	RESZ 811
ID|FBti0027408
SYM|flea{}Dat<up>lo</up>a
SYN|blastopia{}412{}Dat<up>lo</up>
|blastopia{}Dat<up>lo</up>a
|flea{}Dat<up>lo</up>a
ASTP|<fbsym>FBtp0011427==flea</fbsym>
DT|1 Mar 2004
|22 Aug 2003
ICL|flea
ID2|FBti0025365
|FBti0014836
ASGN|<fbsym>FBgn0019643==Dat</fbsym>
SK|FBst0003193
|bw[1] <fbsym>FBal0002239==Dat[lo]</fbsym>
|Total=1

REFDSR
{
RDID|FBrf0103242
|Brodbeck et al.
|1998
SYN|blastopia{}Dat<up>lo</up>a
|flea{}Dat<up>lo</up>a
ASAL|<fbsym>FBal0002239==Dat<up>lo</up></fbsym>
CLOC|60B12--C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0019643==Dat</fbsym>
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
CC|One of two insertions associated with this allele; see <fbsym>FBti0025366==412{}Dat<up>lo</up>b</fbsym>.
}

REF
{
REFM|FBrf0103242
|Brodbeck et al.
|1998
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0002239==Dat<up>lo</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Dopamine acetyltransferase activity low and relative thermolabile.
|<fbsym>FBgn0019643==Dat</fbsym><up>+</up>/<fbsym>Dat&lt;up&gt;lo&lt;/up&gt;</fbsym> activity level intermediate
| between those of the two
|homozygous genotypes.
}

REFDSR
{
RDID|FBrf0126795
|Shaw et al.
|2000
PHP|Homozygous flies do not differ from wild-type flies in the percentage
|and distribution of rest and waking and show normal amounts and patterns
|of activity. However, after 12 hours of rest deprivation during the
|dark period, homozygous flies display a rest rebound that is greater
|than in rest-deprived control flies.
|<fbsym>FBal0002239==Dat<up>lo</up></fbsym>/<fbsym>FBab0002026==Df(2R)Px1</fbsym> flies do not differ
| from <fbsym>FBal0002239==Dat<up>lo</up></fbsym> homozygotes
|or wild-type flies in the percentage and circadian distribution of
|... (see <fbsym>FBal0002239==Dat<up>lo</up></fbsym> report)
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0126795
|Shaw et al.
|2000
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027414	ICL 1 gypsy	SYM 1 gypsy{}tsr<up>ntf</up>	ASTR 1 -	CLOC 1 60B5	REF 1 2	DT 1 22 Aug 2003	RESZ 606
ID|FBti0027414
SYM|gypsy{}tsr<up>ntf</up>
ASTP|<fbsym>FBtp0011429==gypsy</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|gypsy
ASGN|<fbsym>FBgn0011726==tsr</fbsym>

REFDSR
{
RDID|FBrf0134796
|Chen et al.
|2001
SYN|gypsy{}tsr<up>ntf</up>
ASAL|<fbsym>FBal0140903==tsr<up>ntf</up></fbsym>
CLOC|60B5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0011726==tsr</fbsym>
PHC|sterile
|semi-lethal | pupal stage
|(with tsr<up>1</up>) female sterile
|(with tsr<up>2</up>) female sterile
|(with tsr<up>1</up>) male sterile | conditional ts
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0134796
|Chen et al.
|2001
}

ALESR
{
ASYM|<fbsym>FBal0140903==tsr<up>ntf</up></fbsym>

REFDSR
{
RDID|FBrf0134796
|Chen et al.
|2001
PHP|Terminal filaments do not form in the larval ovary of homozygotes at
|25<up>o</up>C, but are formed at 18<up>o</up>C. At 21<up>o</up>C, terminal
| filaments form
|but are not as organized and do not contain as many cells as those
|in wild-type ovaries. At 25<up>o</up>C, the terminal filaments and apical
|cells of the ovary are larger and rounder than normal and the anterior
|region of the ovary appears elongated. There is a large increase in
|the amount of filamentous actin in apical and terminal filament cells
|... (see <fbsym>FBal0140903==tsr<up>ntf</up></fbsym> report)
PHM|terminal filament | conditional ts
|(with tsr<up>1</up>) border follicle cell | conditional ts
|chaeta
|ovary | conditional ts
|actin filament | conditional ts
|(with tsr<up>1</up>) nurse cell & nucleus
}

REF
{
REFM|FBrf0134796
|Chen et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027430	ICL 1 F	SYM 1 F{}y<up>TDF</up>	ASTR 1 -	CLOC 1 1A5	REF 1 2	DT 1 22 Aug 2003	RESZ 492
ID|FBti0027430
SYM|F{}y<up>TDF</up>
ASTP|<fbsym>FBtp0011425==F-element</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|F
ASGN|<fbsym>FBgn0004034==y</fbsym>

REFDSR
{
RDID|FBrf0158980
|Savitsky et al.
|2003
SYN|F{}y<up>TDF</up>
ASAL|<fbsym>FBal0146650==y<up>TDF</up></fbsym>
CLOC|1A5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0004034==y</fbsym>
ABA|Aberration <fbsym>FBab0031284==Df(1)y<up>TDF</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158980
|Savitsky et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0146650==y<up>TDF</up></fbsym>

REFDSR
{
RDID|FBrf0158980
|Savitsky et al.
|2003
PHP|Body color: flies carrying <fbsym>FBal0146650==y<up>TDF</up></fbsym> (in a <fbsym>FBgn0004034==y</fbsym><up>-</up>
| background) have
|a pigmentation score of 1 (where 1 = absence of <fbsym>FBgn0004034==y</fbsym> expression and
|5 = wild type) in both the body and wing.
|Body color: <fbsym>FBal0146650==y<up>TDF</up></fbsym>/<fbsym>FBal0036033==y<up>1#8</up></fbsym> flies
| have a pigmentation score of 4
|in both the body and wing.
|Body color: <fbsym>FBal0146650==y<up>TDF</up></fbsym>/<fbsym>FBal0018630==y<up>59b</up></fbsym> flies
| have a pigmentation score of 4
|in both the body and wing.
PHM|adult cuticle
|wing
|(with y<up>1#8</up>) adult cuticle
|(with y<up>1#8</up>) wing
|(with y<up>59b</up>) adult cuticle
|(with y<up>59b</up>) wing
}

REF
{
REFM|FBrf0158980
|Savitsky et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027457	ICL 1 P	SYM 1 P{}rigel<up>P</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 22 Aug 2003	RESZ 398
ID|FBti0027457
SYM|P{}rigel<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0066329==rigel</fbsym>

REFDSR
{
RDID|FBrf0150723
|Riede
|2001
SYN|P{}rigel<up>P</up>
ASAL|<fbsym>FBal0146848==rigel<up>P</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0066329==rigel</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0150723
|Riede
|2001
}

ALESR
{
ASYM|<fbsym>FBal0146848==rigel<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0150723
|Riede
|2001
PHP|Shows lethality from the embryonic to the pupal stage when heterozygous
|with the MBT chromosome.
}

REF
{
REFM|FBrf0150723
|Riede
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027460	ICL 1 P	SYM 1 P{lacZ}pxb<up>baikal</up>	ASTR 1 -	CLOC 1 89A1--2	REF 1 2	DT 1 22 Aug 2003	RESZ 552
ID|FBti0027460
SYM|P{lacZ}pxb<up>baikal</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0053207==pxb</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
SYN|P{lacZ}pxb<up>baikal</up>
ASAL|<fbsym>FBal0147951==Ecol\lacZ<up>pxb-baikal</up></fbsym>
|<fbsym>FBal0146873==pxb<up>baikal</up></fbsym>
CLOC|89A1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0053207==pxb</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159552
|Dubnau et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0146873==pxb<up>baikal</up></fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
PHP|In memory tests, mutants perform at 123% of wild-type after a single
|training session, at 28% after spaced training.
}

REF
{
REFM|FBrf0159552
|Dubnau et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027499	ICL 1 P	SYM 1 P{lacZ}cher<up>joy</up>	ASTR 1 -	CLOC 1 89E12--13	REF 1 2	DT 1 22 Aug 2003	RESZ 548
ID|FBti0027499
SYM|P{lacZ}cher<up>joy</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0014141==cher</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
SYN|P{lacZ}cher<up>joy</up>
ASAL|<fbsym>FBal0147230==cher<up>joy</up></fbsym>
|<fbsym>FBal0147978==Ecol\lacZ<up>cher-joy</up></fbsym>
CLOC|89E12--13
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0014141==cher</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159552
|Dubnau et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0147230==cher<up>joy</up></fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
PHP|In memory tests, mutants perform at 104% of wild-type after a single
|training session, at 24% after spaced training.
}

REF
{
REFM|FBrf0159552
|Dubnau et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027503	ICL 1 P	SYM 1 P{}btx<up>P</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 22 Aug 2003	RESZ 388
ID|FBti0027503
SYM|P{}btx<up>P</up>
ASTP|<fbsym>FBtp0011456==P-element</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0066370==btx</fbsym>

REFDSR
{
RDID|FBrf0150723
|Riede
|2001
SYN|P{}btx<up>P</up>
ASAL|<fbsym>FBal0147247==btx<up>P</up></fbsym>
LOCB|Proximity to gene: <fbsym>FBgn0066370==btx</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0150723
|Riede
|2001
}

ALESR
{
ASYM|<fbsym>FBal0147247==btx<up>P</up></fbsym>

REFDSR
{
RDID|FBrf0150723
|Riede
|2001
PHP|Embryonic lethal when heterozygous with the MBT chromosome.
}

REF
{
REFM|FBrf0150723
|Riede
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027575	ICL 1 P	SYM 1 P{lacZ}Gclm<up>box</up>	ASTR 1 -	CLOC 1 94C1	REF 1 2	DT 1 22 Aug 2003	RESZ 543
ID|FBti0027575
SYM|P{lacZ}Gclm<up>box</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0046114==Gclm</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
SYN|P{lacZ}Gclm<up>box</up>
ASAL|<fbsym>FBal0148026==Ecol\lacZ<up>Gclm-box</up></fbsym>
|<fbsym>FBal0147900==Gclm<up>box</up></fbsym>
CLOC|94C1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0046114==Gclm</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159552
|Dubnau et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0147900==Gclm<up>box</up></fbsym>

REFDSR
{
RDID|FBrf0159552
|Dubnau et al.
|2003
PHP|In memory tests, mutants perform at 110% of wild-type after a single
|training session, at 39% after spaced training.
}

REF
{
REFM|FBrf0159552
|Dubnau et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0027580	ICL 1 P	SYM 1 P{PZ}Dad<up>PZ</up>	ASTR 1 -	CLOC 1 89E11	REF 1 2	DT 1 22 Aug 2003	RESZ 559
ID|FBti0027580
SYM|P{PZ}Dad<up>PZ</up>
SYN|Dad-lacZ
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|22 Aug 2003
|22 Aug 2003
ICL|P
ASGN|<fbsym>FBgn0020493==Dad</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0159297
|Kai and Spradling
|2003
SYN|Dad-lacZ
|P{PZ}Dad<up>PZ</up>
ASAL|<fbsym>FBal0148085==Dad<up>PZ</up></fbsym>
|<fbsym>FBal0148030==Ecol\lacZ<up>Dad-PZ</up></fbsym>
CLOC|89E11
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0020493==Dad</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159297
|Kai and Spradling
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027617	ICL 1 P	SYM 1 P{HSPB}sy	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 24 Aug 2003	RESZ 338
ID|FBti0027617
SYM|P{HSPB}sy
SYN|HSPB<up>sy</up>
ASTP|<fbsym>FBtp0003763==P{HSPB}</fbsym>
DT|24 Aug 2003
|22 Aug 2003
ICL|P

REFDSR
{
RDID|FBrf0155717
|Benassayag et al.
|2003
SYN|HSPB<up>sy</up>
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155717
|Benassayag et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027716	ICL 1 P	SYM 1 P{UAS-Thor.LL}w	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 24 Aug 2003	RESZ 295
ID|FBti0027716
SYM|P{UAS-Thor.LL}w
SYN|d4E-BP(LL)<up>w</up>
ASTP|<fbsym>FBtp0017257==P{UAS-Thor.LL}</fbsym>
DT|24 Aug 2003
|22 Aug 2003
ICL|P

REFDSR
{
RDID|FBrf0137059
|Miron et al.
|2001
SYN|d4E-BP(LL)<up>w</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137059
|Miron et al.
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027717	ICL 1 P	SYM 1 P{UAS-Thor.LL}s	ASTR 1 -	CLOC 1 61-100	REF 1 3	DT 1 24 Aug 2003	RESZ 571
ID|FBti0027717
SYM|P{UAS-Thor.LL}s
SYN|d4E-BP(LL)<up>s</up>
ASTP|<fbsym>FBtp0017257==P{UAS-Thor.LL}</fbsym>
DT|24 Aug 2003
|22 Aug 2003
ICL|P
SK|FBst0008651
|w[*]; P{w[+mC]=UAS-p35.H}BH1; P{w[+mC]=UAS-Thor.LL}s
|Total=1

REFDSR
{
RDID|FBrf0137059
|Miron et al.
|2001
SYN|d4E-BP(LL)<up>s</up>
}

REFDSR
{
RDID|FBrf0183109
|Levine and Lasko
|2004.12
SYN|P{UAS-Thor.LL}s
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0137059
|Miron et al.
|2001
REFM|FBrf0183109
|Levine and Lasko
|2004.12
}

}

# EOR

TIR
{

RETE|ID 1 FBti0027903	ICL 1 P	SYM 1 P{UAS-rib.B}HVII	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 24 Aug 2003	RESZ 398
ID|FBti0027903
SYM|P{UAS-rib.B}HVII
ASTP|<fbsym>FBtp0014785==P{UAS-rib.B}</fbsym>
DT|24 Aug 2003
|22 Aug 2003
ICL|P
SK|FBst0007095
|w[1118]; P{w[+mC]=UAS-rib.B}HVII
|Total=1

REFDSR
{
RDID|FBrf0159889
|Lengyel
|2003.7.4
SYN|P{UAS-rib.B}HVII
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
PHC|viable
|fertile
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159889
|Lengyel
|2003.7.4
}

}

# EOR

TIR
{

RETE|ID 1 FBti0037935	ICL 1 ?	SYM 1 ?{}lz<up>L</up>	ASTR 1 -	CLOC 1 8D5--6	REF 1 2	DT 1 21 Oct 2003	RESZ 436
ID|FBti0037935
SYM|?{}lz<up>L</up>
DT|21 Oct 2003
|21 Oct 2003
ICL|?
ASGN|<fbsym>FBgn0002576==lz</fbsym>
SK|FBst0007366
|lz[L]/Dp(1;Y)lz[+]/FM7a
|Total=1

REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
SYN|?{}lz<up>L</up>
ASAL|<fbsym>FBal0061066==lz<up>L</up></fbsym>
CLOC|8D5--6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002576==lz</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158867
|Siddall et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0061066==lz<up>L</up></fbsym>

REFDSR
{
RDID|FBrf0068701
|Stocker et al.
|1993
PHP|The antennal funiculus is reduced in size in hemizygous males. All
|large and small basiconic sensilla on the antennal funiculus are missing,
|and the number of trichoid sensilla on the antennal funiculus is reduced.
|The number of coeloconic sensilla on the antennal funiculus is normal.
|The density of the coeloconic sensilla on the antennal funiculus is
|increased and the density of the trichoid sensilla on the antennal
|funiculus is decreased compared to wild-type.
|... (see <fbsym>FBal0061066==lz<up>L</up></fbsym> report)
PHM|antennal segment 3
|sensillum basiconicum of antennal segment 3
|sensillum trichodeum of antennal segment 3
|maxillary palp sensillum basiconicum
}

REFDSR
{
RDID|FBrf0090446
|Batterham et al.
|1996
PHP|Homozygotes have a total lack of ommatidial structure in the eye.
|Pigment is dispersed as a ring around the edge of the eye ("spectacle"
|phenotype). Few, if any lenses form, and the eye is covered by a cuticle
|scar. The 'retina' appears to lack pigment cells. Photoreceptor cell
|orientation is random, and the fenestrated membrane is absent.
PHM|eye
|ommatidium
|lens
|photoreceptor cell
|pigment cell
}

REFDSR
{
RDID|FBrf0093407
|Crew et al.
|1997
PHP|15% of photoreceptor cell clusters are abnormal, cells R1 and R6 are
|not recruited properly. Uniform sheet of unorganized cone cells is
|found. The periphery of the retina contains cells in loosely organized
|clusters including cones as well as primary and secondary pigment cells,
|the darker pigment produces the 'spectacle' phenotype.
PHM|photoreceptor cell R1
|photoreceptor cell R6
|cone cell
}

REFDSR
{
RDID|FBrf0158867
|Siddall et al.
|2003
PHP|<fbsym>FBal0061066==lz<up>L</up></fbsym> adults have a "spectacle" eye phenotype.
| Ommatidial clusters
|are rarely detectable in <fbsym>FBal0061066==lz<up>L</up></fbsym> eyes. Ectopic cell
| death is seen
|in third larval instar eye discs, between rows 3 an 7 posterior to
|the morphogenetic furrow.
PHM|ommatidium
|eye disc
|eye
}

REF
{
REFM|FBrf0068701
|Stocker et al.
|1993
REFM|FBrf0090446
|Batterham et al.
|1996
REFM|FBrf0093407
|Crew et al.
|1997
REFM|FBrf0158867
|Siddall et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0037956	ICL 1 P	SYM 1 P{GawB}Va	ASTR 1 -	CLOC 1 -	REF 1 3	DT 1 21 Oct 2003	RESZ 417
ID|FBti0037956
SYM|P{GawB}Va
SYN|Va<up>GAL4</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|21 Oct 2003
|21 Oct 2003
ICL|P
ASGN|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0158766
|Allan et al.
|2003
SYN|P{GawB}Va
|Va<up>GAL4</up>
ASAL|<fbsym>FBal0150623==Scer\GAL4<up>Va</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0158766
|Allan et al.
|2003
REFM|FBrf0161463
|Allan et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0037957	ICL 1 P	SYM 1 P{GawB}MzVum	ASTR 1 -	CLOC 1 5A3--5	REF 1 2	DT 1 21 Oct 2003	RESZ 632
ID|FBti0037957
SYM|P{GawB}MzVum
SYN|MzVum-Gal4
|MzVUM-Gal4
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|21 Oct 2003
|21 Oct 2003
ICL|P
ASGN|<fbsym>FBgn0053980==CG33980</fbsym>
|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0160715
|Landgraf et al.
|2003
SYN|MzVum-Gal4
|MzVum-Gal4
|MzVUM-Gal4
|P{GawB}MzVum
ASAL|<fbsym>FBal0150624==Scer\GAL4<up>MzVum</up></fbsym>
CLOC|5A3--5
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0053980==CG33980</fbsym>
CC|Insertion site is 886 base pairs upstream of <fbsym>FBgn0029774==CG15781</fbsym>.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0160715
|Landgraf et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0037958	ICL 1 P	SYM 1 P{GawB}MzCh	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 21 Oct 2003	RESZ 380
ID|FBti0037958
SYM|P{GawB}MzCh
SYN|MzCh-Gal4
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|21 Oct 2003
|21 Oct 2003
ICL|P
ASGN|<fbsym>FBgn0014445==Scer\GAL4</fbsym>

REFDSR
{
RDID|FBrf0160715
|Landgraf et al.
|2003
SYN|MzCh-Gal4
|P{GawB}MzCh
ASAL|<fbsym>FBal0150625==Scer\GAL4<up>MzCh</up></fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0160715
|Landgraf et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0037978	ICL 1 P	SYM 1 P{UAS-pum.S}II	ASTR 1 -	CLOC 1 21-60	REF 1 2	DT 1 23 Oct 2003	RESZ 333
ID|FBti0037978
SYM|P{UAS-pum.S}II
SYN|UAS-pumII
ASTP|<fbsym>FBtp0017593==P{UAS-pum.S}</fbsym>
DT|23 Oct 2003
|22 Oct 2003
ICL|P

REFDSR
{
RDID|FBrf0151333
|Schweers et al.
|2002
SYN|UAS-pumII
GLOC|21-60
|Insertion site 
LOCB|Mapped to chromosome #2
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0151333
|Schweers et al.
|2002
}

}

# EOR

TIR
{

RETE|ID 1 FBti0038272	ICL 1 P	SYM 1 P{PZ}edl<up>JV</up>	ASTR 1 -	CLOC 1 55E6	REF 1 2	DT 1 3 Mar 2004	RESZ 512
ID|FBti0038272
SYM|P{PZ}edl<up>JV</up>
SYN|JV
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|3 Mar 2004
|3 Mar 2004
ICL|P
PRG|<fbsym>FBti0038426==P{PZ}P17</fbsym>
ASGN|<fbsym>FBgn0023214==edl</fbsym>

REFDSR
{
RDID|FBrf0161068
|Yamada et al.
|2003
SYN|JV
|P{PZ}edl<up>JV</up>
ASAL|<fbsym>FBal0151999==edl<up>JV</up></fbsym>
CLOC|55E6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0023214==edl</fbsym>
PHC|(with Df(2R)P34) lethal
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0161068
|Yamada et al.
|2003
}

ALESR
{
ASYM|<fbsym>FBal0151999==edl<up>JV</up></fbsym>

REFDSR
{
RDID|FBrf0161068
|Yamada et al.
|2003
PHP|<fbsym>FBal0151999==edl<up>JV</up></fbsym>/<fbsym>FBab0002011==Df(2R)P34</fbsym> animals show 5% viability.
|About 3% of ommatidia show loss of R1-R6 and R7 photoreceptor cells
|in <fbsym>FBal0151999==edl<up>JV</up></fbsym>/<fbsym>FBab0002011==Df(2R)P34</fbsym> and
| <fbsym>FBal0151999==edl<up>JV</up></fbsym>/<fbsym>FBab0037748==Df(2R)edl-L19</fbsym> animals.
PHM|(with Df(2R)P34) photoreceptor cell R1
|(with Df(2R)P34) photoreceptor cell R2
|(with Df(2R)P34) photoreceptor cell R3
|(with Df(2R)P34) photoreceptor cell R4
|(with Df(2R)P34) photoreceptor cell R5
|(with Df(2R)P34) photoreceptor cell R6
|(with Df(2R)P34) photoreceptor cell R7
|(with Df(2R)edl-L19) photoreceptor cell R1
|(with Df(2R)edl-L19) photoreceptor cell R2
|(with Df(2R)edl-L19) photoreceptor cell R3
|(with Df(2R)edl-L19) photoreceptor cell R4
|(with Df(2R)edl-L19) photoreceptor cell R5
|(with Df(2R)edl-L19) photoreceptor cell R6
|(with Df(2R)edl-L19) photoreceptor cell R7
}

REF
{
REFM|FBrf0161068
|Yamada et al.
|2003
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0038273	ICL 1 P	SYM 1 P{PZ}edl<up>JS</up>	ASTR 1 -	CLOC 1 55E6	REF 1 2	DT 1 3 Mar 2004	RESZ 577
ID|FBti0038273
SYM|P{PZ}edl<up>JS</up>
SYN|JS
ASTP|<fbsym>FBtp0000210==P{PZ}</fbsym>
DT|3 Mar 2004
|3 Mar 2004
ICL|P
PRG|<fbsym>FBti0038426==P{PZ}P17</fbsym>
ASGN|<fbsym>FBgn0023214==edl</fbsym>
|<fbsym>FBgn0014447==Ecol\lacZ</fbsym>

REFDSR
{
RDID|FBrf0161068
|Yamada et al.
|2003
SYN|JS
|P{PZ}edl<up>JS</up>
ASAL|<fbsym>FBal0152563==Ecol\lacZ<up>edl-JS</up></fbsym>
|<fbsym>FBal0152000==edl<up>JS</up></fbsym>
CLOC|55E6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0023214==edl</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0161068
|Yamada et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0038523	ICL 1 P	SYM 1 P{UAS-spen.DN}II	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 3 Mar 2004	RESZ 314
ID|FBti0038523
SYM|P{UAS-spen.DN}II
SYN|[UAS-spen<up>DN</up>]<up>II</up>
ASTP|<fbsym>FBtp0017803==P{UAS-spen.DN}</fbsym>
DT|3 Mar 2004
|3 Mar 2004
ICL|P

REFDSR
{
RDID|FBrf0160742
|Lin et al.
|2003
SYN|[UAS-spen<up>DN</up>]<up>II</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0160742
|Lin et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0038524	ICL 1 P	SYM 1 P{UAS-spen.DN}III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 3 Mar 2004	RESZ 317
ID|FBti0038524
SYM|P{UAS-spen.DN}III
SYN|[UAS-spen<up>DN</up>]<up>III</up>
ASTP|<fbsym>FBtp0017803==P{UAS-spen.DN}</fbsym>
DT|3 Mar 2004
|3 Mar 2004
ICL|P

REFDSR
{
RDID|FBrf0160742
|Lin et al.
|2003
SYN|[UAS-spen<up>DN</up>]<up>III</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0160742
|Lin et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0038597	ICL 1 P	SYM 1 P{UAS-odd.H}A	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 3 Mar 2004	RESZ 263
ID|FBti0038597
SYM|P{UAS-odd.H}A
SYN|UASodd[A]
ASTP|<fbsym>FBtp0017880==P{UAS-odd.H}</fbsym>
DT|3 Mar 2004
|3 Mar 2004
ICL|P

REFDSR
{
RDID|FBrf0167461
|Hao et al.
|2003
SYN|UASodd[A]
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0167461
|Hao et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0040492	ICL 1 P	SYM 1 P{UAS-endo.V}I-III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 25 Aug 2004	RESZ 341
ID|FBti0040492
SYM|P{UAS-endo.V}I-III
SYN|P{w<up>+</up>,UAS-endo<up>I-III</up>}
ASTP|<fbsym>FBtp0018408==P{UAS-endo.V}</fbsym>
DT|25 Aug 2004
|25 Aug 2004
ICL|P

REFDSR
{
RDID|FBrf0167964
|Verstreken et al.
|2003
SYN|P{w<up>+</up>,UAS-endo<up>I-III</up>}
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0167964
|Verstreken et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0040526	ICL 1 P	SYM 1 P{UAS-ed.B}X	ASTR 1 -	CLOC 1 1-20	REF 1 2	DT 1 25 Aug 2004	RESZ 343
ID|FBti0040526
SYM|P{UAS-ed.B}X
SYN|UAS-ed<up>X</up>
ASTP|<fbsym>FBtp0013891==P{UAS-ed.B}</fbsym>
DT|25 Aug 2004
|25 Aug 2004
ICL|P

REFDSR
{
RDID|FBrf0167516
|Escudero et al.
|2003
SYN|UAS-ed<up>X</up>
GLOC|1-20
|Insertion site 
LOCB|Mapped to chromosome #1
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0167516
|Escudero et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0040527	ICL 1 P	SYM 1 P{UAS-ed.B}III	ASTR 1 -	CLOC 1 61-100	REF 1 2	DT 1 25 Aug 2004	RESZ 351
ID|FBti0040527
SYM|P{UAS-ed.B}III
SYN|UAS-ed<up>III</up>
ASTP|<fbsym>FBtp0013891==P{UAS-ed.B}</fbsym>
DT|25 Aug 2004
|25 Aug 2004
ICL|P

REFDSR
{
RDID|FBrf0167516
|Escudero et al.
|2003
SYN|UAS-ed<up>III</up>
GLOC|61-100
|Insertion site 
LOCB|Mapped to chromosome #3
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0167516
|Escudero et al.
|2003
}

}

# EOR

TIR
{

RETE|ID 1 FBti0040835	ICL 1 P	SYM 1 P{UASp-nod-GFP}III	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 25 Aug 2004	RESZ 305
ID|FBti0040835
SYM|P{UASp-nod-GFP}III
SYN|UAS-nod-GFP (III)
ASTP|<fbsym>FBtp0014112==P{UASp-nod-GFP}</fbsym>
DT|25 Aug 2004
|25 Aug 2004
ICL|P

REFDSR
{
RDID|FBrf0167530
|Murthy and Schwarz
|2004
SYN|UAS-nod-GFP (III)
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0167530
|Murthy and Schwarz
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0058521	ICL 1 P	SYM 1 P{GawB}dac<up>PG</up>	ASTR 1 -	CLOC 1 36A1--2	REF 1 2	DT 1 5 Jan 2005	RESZ 445
ID|FBti0058521
SYM|P{GawB}dac<up>PG</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|5 Jan 2005
|5 Jan 2005
ICL|P
ASGN|<fbsym>FBgn0005677==dac</fbsym>

REFDSR
{
RDID|FBrf0179474
|Tavsanli et al.
|2004
SYN|P{GawB}dac<up>PG</up>
ASAL|<fbsym>FBal0159341==dac<up>PG</up></fbsym>
CLOC|36A1--2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0005677==dac</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0179474
|Tavsanli et al.
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0058613	ICL 1 P	SYM 1 P{UAS-wee.P}VIII	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 6 Jan 2005	RESZ 282
ID|FBti0058613
SYM|P{UAS-wee.P}VIII
SYN|UAS-dwee1VIII
ASTP|<fbsym>FBtp0015958==P{UAS-wee.P}</fbsym>
DT|6 Jan 2005
|6 Jan 2005
ICL|P

REFDSR
{
RDID|FBrf0174447
|Reis and Edgar
|2004
SYN|UAS-dwee1VIII
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0174447
|Reis and Edgar
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0058724	ICL 1 PBac	SYM 1 PBac{PBss}scarface<up>PBss</up>	ASTR 1 -	CLOC 1 41F8	REF 1 2	DT 1 6 Jan 2005	RESZ 478
ID|FBti0058724
SYM|PBac{PBss}scarface<up>PBss</up>
ASTP|<fbsym>FBtp0019241==PBac{PBss}</fbsym>
DT|6 Jan 2005
|6 Jan 2005
ICL|PBac
ASGN|<fbsym>FBgn0033033==scarface</fbsym>

REFDSR
{
RDID|FBrf0179794
|Bonin
|2004
SYN|PBac{PBss}scarface<up>PBss</up>
ASAL|<fbsym>FBal0158698==scarface<up>PBss</up></fbsym>
CLOC|41F8
LOCB|genomic location inferred from flanking sequence
PHC|lethal | pupal stage | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0179794
|Bonin
|2004
}

ALESR
{
ASYM|<fbsym>FBal0158698==scarface<up>PBss</up></fbsym>

REFDSR
{
RDID|FBrf0179794
|Bonin
|2004
PHP|Homozygous adult escapers have what appears to be "scarring" around
|the mouthparts that is indicative of necrotic tissue.
PHM|adult head
}

REF
{
REFM|FBrf0179794
|Bonin
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0058731	ICL 1 PBac	SYM 1 PBac{PBss}Idh<up>PBss</up>	ASTR 1 -	CLOC 1 66C8	REF 1 2	DT 1 6 Jan 2005	RESZ 444
ID|FBti0058731
SYM|PBac{PBss}Idh<up>PBss</up>
ASTP|<fbsym>FBtp0019241==PBac{PBss}</fbsym>
DT|6 Jan 2005
|6 Jan 2005
ICL|PBac
ASGN|<fbsym>FBgn0001248==Idh</fbsym>

REFDSR
{
RDID|FBrf0179794
|Bonin
|2004
SYN|PBac{PBss}Idh<up>PBss</up>
ASAL|<fbsym>FBal0160289==Idh<up>PBss</up></fbsym>
CLOC|66C8
LOCB|genomic location inferred from flanking sequence
PHC|lethal | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0179794
|Bonin
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0058809	ICL 1 P	SYM 1 P{UAS-Pvr.dsRNA.R}GOF	ASTR 1 -	CLOC 1 27A1-27A2	REF 1 2	DT 1 6 Jan 2005	RESZ 557
ID|FBti0058809
SYM|P{UAS-Pvr.dsRNA.R}GOF
SYN|RNAi-GOF
|UAS-RNAi-GOF
ASTP|<fbsym>FBtp0019070==P{UAS-Pvr.dsRNA.R}</fbsym>
DT|6 Jan 2005
|6 Jan 2005
ICL|P

REFDSR
{
RDID|FBrf0174570
|Rosin et al.
|2004
SYN|RNAi-GOF
|UAS-RNAi-GOF
CLOC|27A1-27A2
|Insertion site 
LOCB|in situ
CC|Levels of <fbsym>FBgn0032006==Pvr</fbsym> mRNA are elevated rather than reduced in
| <fbsym>FBti0058809==P{UAS-Pvr.dsRNA.R}GOF</fbsym>; <fbsym>FBal0052396==Scer\GAL4<up>unspecified</up></fbsym>animals.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0174570
|Rosin et al.
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0064342	ICL 1 P	SYM 1 P{EP}comm<up>EP</up>	ASTR 1 -	CLOC 1 71F2	REF 1 2	DT 1 28 Apr 2005	RESZ 462
ID|FBti0064342
SYM|P{EP}comm<up>EP</up>
SYN|EP-comm
ASTP|<fbsym>FBtp0001317==P{EP}</fbsym>
DT|28 Apr 2005
|28 Apr 2005
ICL|P
ASGN|<fbsym>FBgn0010105==comm</fbsym>

REFDSR
{
RDID|FBrf0180051
|Kraut and Zinn
|2004
SYN|EP-comm
|P{EP}comm<up>EP</up>
ASAL|<fbsym>FBal0175733==comm<up>EP</up></fbsym>
CLOC|71F2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0010105==comm</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0180051
|Kraut and Zinn
|2004
}

ALESR
{
ASYM|<fbsym>FBal0175733==comm<up>EP</up></fbsym>

REFDSR
{
RDID|FBrf0180051
|Kraut and Zinn
|2004
PHP|20.4% of thoracic segments show transformation of the dch3 chordotonal
|organs to a morphology resembling that of abdominal lch5 chordotonal
|organs in embryos expressing <fbsym>FBal0175733==comm<up>EP</up></fbsym> under the
| control of <fbsym>FBal0063393==Scer\GAL4<up>48Y</up></fbsym>.
PHM|mesothoracic dorsal triscolopidial chordotonal organ dch3 with <fbsym>FBal0063393==Scer\GAL4<up>48Y</up></fbsym>
|metathoracic dorsal triscolopidial chordotonal organ dch3 with <fbsym>FBal0063393==Scer\GAL4<up>48Y</up></fbsym>
}

REF
{
REFM|FBrf0180051
|Kraut and Zinn
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0064515	ICL 1 P	SYM 1 P{lyB}Alh<up>y+</up>	ASTR 1 -	CLOC 1 84B6--C3	REF 1 3	DT 1 28 Apr 2005	RESZ 511
ID|FBti0064515
SYM|P{lyB}Alh<up>y+</up>
ASTP|<fbsym>FBtp0012979==P{lyB}</fbsym>
DT|28 Apr 2005
|28 Apr 2005
ICL|P
ASGN|<fbsym>FBgn0037471==Alh</fbsym>
SK|FBst0008642
|y[1] w[67c23]; Ki[1] P{y[+mDint]=lyB}Alh[y+]
|Total=1

REFDSR
{
RDID|FBrf0155962 
SYN|P{lyB}Alh<up>y+</up>
ASAL|<fbsym>FBal0176400==Alh<up>y+</up></fbsym>
CLOC|84B6--C3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0037471==Alh</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155962 
REFM|FBrf0180544
|Perrin and Dura
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0072123	ICL 1 P	SYM 1 P{lacW}ru<up>inga</up>	ASTR 1 -	CLOC 1 61F8	REF 1 2	DT 1 29 Nov 2005	RESZ 456
ID|FBti0072123
SYM|P{lacW}ru<up>inga</up>
SYN|inga
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|P
ASGN|<fbsym>FBgn0003295==ru</fbsym>

REFDSR
{
RDID|FBrf0179216
|Gallio et al.
|2004
SYN|inga
|P{lacW}ru<up>inga</up>
ASAL|<fbsym>FBal0178144==ru<up>inga</up></fbsym>
CLOC|61F8
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003295==ru</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0179216
|Gallio et al.
|2004
}

ALESR
{
ASYM|<fbsym>FBal0178144==ru<up>inga</up></fbsym>

REFDSR
{
RDID|FBrf0179216
|Gallio et al.
|2004
PHP|In stage 16 <fbsym>ru<up>inga</up></fbsym> mutant and
| <fbsym>ru<up>inga</up></fbsym>/<fbsym>FBab0010230==Df(3L)Ar14-8</fbsym> embryos,
|a significant number of ganglionic branch trachea fail to turn posteriorly
|and dorsally at the ventral midline and instead cross the midline or
|remain lingering on it.
PHM|embryonic/larval ganglionic branch
|(with Df(3L)Ar14-8) embryonic/larval ganglionic branch
}

REF
{
REFM|FBrf0179216
|Gallio et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0072160	ICL 1 roo	SYM 1 roo{}mats<up>roo</up>	ASTR 1 -	CLOC 1 94A12	REF 1 2	DT 1 29 Nov 2005	RESZ 489
ID|FBti0072160
SYM|roo{}mats<up>roo</up>
ASTP|<fbsym>FBtp0011460==roo</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|roo
ASGN|<fbsym>FBgn0038965==mats</fbsym>

REFDSR
{
RDID|FBrf0183777
|Lai et al.
|2005
SYN|roo{}mats<up>roo</up>
ASAL|<fbsym>FBal0178932==mats<up>roo</up></fbsym>
CLOC|94A12
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0038965==mats</fbsym>
PHC|lethal | second instar larval stage | recessive
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0183777
|Lai et al.
|2005
}

ALESR
{
ASYM|<fbsym>FBal0178932==mats<up>roo</up></fbsym>

REFDSR
{
RDID|FBrf0183777
|Lai et al.
|2005
PHP|When <fbsym>mats<up>roo</up></fbsym> mutant clones are made, large tumors
| can be induced
|in many organs, including the head, notum, eye wing, antenna and halteres.
|The tumor cells form unpatterned tissues with many folds on the surface,
|the mutant cells clearly overproliferating. Cell sized is not significantly
|different from wild-type.
|When clones are made in the larval eye discs, photoreceptors and cone
|cells appear to be specified normally, however they fail to fully differentiate
|... (see <fbsym>mats<up>roo</up></fbsym> report)
}

REF
{
REFM|FBrf0183777
|Lai et al.
|2005
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0072213	ICL 1 P	SYM 1 P{GS}ds<up>GS.D</up>	ASTR 1 -	CLOC 1 21E2	REF 1 2	DT 1 29 Nov 2005	RESZ 454
ID|FBti0072213
SYM|P{GS}ds<up>GS.D</up>
SYN|GS-ds
ASTP|<fbsym>FBtp0011344==P{GS}</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|P
ASGN|<fbsym>FBgn0000497==ds</fbsym>

REFDSR
{
RDID|FBrf0180144
|Cho and Irvine
|2004
SYN|GS-ds
|P{GS}ds<up>GS.D</up>
ASAL|<fbsym>FBal0180101==ds<up>GS.D</up></fbsym>
CLOC|21E2
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000497==ds</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0180144
|Cho and Irvine
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0072309	ICL 1 P	SYM 1 P{GawB}Bx<up>pdrm</up>	ASTR 1 -	CLOC 1 17C3--4	REF 1 2	DT 1 29 Nov 2005	RESZ 495
ID|FBti0072309
SYM|P{GawB}Bx<up>pdrm</up>
ASTP|<fbsym>FBtp0000352==P{GawB}</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|P
ASGN|<fbsym>FBgn0000242==Bx</fbsym>

REFDSR
{
RDID|FBrf0180477
|Tsai et al.
|2004
SYN|P{GawB}Bx<up>pdrm</up>
ASAL|<fbsym>FBal0187950==Bx<up>pdrm</up></fbsym>
|<fbsym>FBal0181671==Scer\GAL4<up>Bx-pdrm</up></fbsym>
CLOC|17C3--4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000242==Bx</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0180477
|Tsai et al.
|2004
}

ALESR
{
ASYM|<fbsym>FBal0187950==Bx<up>pdrm</up></fbsym>

REFDSR
{
RDID|FBrf0180477
|Tsai et al.
|2004
PHP|Mutant animals exhibit an increased sensitivity to cocaine.
|The number and detailed morphology of LN<down>v</down> neurons is normal in
|mutant animals.
}

REF
{
REFM|FBrf0180477
|Tsai et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0072373	ICL 1 P	SYM 1 P{lacZ}HGTX<up>P-JG</up>	ASTR 1 -	CLOC 1 70E3	REF 1 2	DT 1 29 Nov 2005	RESZ 516
ID|FBti0072373
SYM|P{lacZ}HGTX<up>P-JG</up>
SYN|P<up>{JG<up>LacZ</up>}</up>
ASTP|<fbsym>FBtp0001402==P{lacZ}</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|P
ASGN|<fbsym>FBgn0040318==HGTX</fbsym>

REFDSR
{
RDID|FBrf0180162
|Broihier et al.
|2004
SYN|P<up>{JG<up>LacZ</up>}</up>
|P{lacZ}HGTX<up>P-JG</up>
ASAL|<fbsym>FBal0183333==HGTX<up>P-JG</up></fbsym>
CLOC|70E3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0040318==HGTX</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0180162
|Broihier et al.
|2004
}

ALESR
{
ASYM|<fbsym>FBal0183333==HGTX<up>P-JG</up></fbsym>

REFDSR
{
RDID|FBrf0180162
|Broihier et al.
|2004
PHP|In stage 16 <fbsym>HGTX<up>D25</up></fbsym>/<fbsym>HGTX<up>P-JG</up></fbsym>
| embryos, both secondary branches
|of the intersegmental nerve (anterior fascicle), ISNb and ISNd, are
|absent in a significant proportion of hemisegments.
PHM|(with HGTX<up>D25</up>) anterior fascicle & stage 16 embryo
}

REF
{
REFM|FBrf0180162
|Broihier et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0072382	ICL 1 P	SYM 1 P{lacW}Fili<up>lacZ</up>	ASTR 1 -	CLOC 1 58A4	REF 1 2	DT 1 29 Nov 2005	RESZ 490
ID|FBti0072382
SYM|P{lacW}Fili<up>lacZ</up>
SYN|fili-lacZ
ASTP|<fbsym>FBtp0000204==P{lacW}</fbsym>
DT|29 Nov 2005
|29 Nov 2005
ICL|P
ASGN|<fbsym>FBgn0034668==Fili</fbsym>

REFDSR
{
RDID|FBrf0184157
|Adachi-Yamada et al.
|2005
SYN|fili-lacZ
|P{lacW}Fili<up>lacZ</up>
ASAL|<fbsym>FBal0183550==Fili<up>lacZ</up></fbsym>
CLOC|58A4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0034668==Fili</fbsym>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184157
|Adachi-Yamada et al.
|2005
}

}

# EOR

TIR
{

RETE|ID 1 FBti0072871	ICL 1 P	SYM 1 P{UAS-Pak.MYC}X	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 30 Nov 2005	RESZ 285
ID|FBti0072871
SYM|P{UAS-Pak.MYC}X
SYN|UAS-Pak<up>X</up>
ASTP|<fbsym>FBtp0017299==P{UAS-Pak.MYC}</fbsym>
DT|30 Nov 2005
|29 Nov 2005
ICL|P

REFDSR
{
RDID|FBrf0180582
|Ng and Luo
|2004
SYN|UAS-Pak<up>X</up>
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0180582
|Ng and Luo
|2004
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018424	ICL 1 3S18	SYM 1 3S18{?'}Dr<up>R10</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Oct 2001	RESZ 547
ID|FBti0018424
SYM|3S18{?'}Dr<up>R10</up>
ASTP|<fbsym>FBtp0014767==3S18{?'}</fbsym>
DT|15 Oct 2001
|3 Oct 2001
ICL|3S18
PRG|<fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>
ASGN|<fbsym>FBgn0000492==Dr</fbsym>

REFDSR
{
RDID|FBrf0136848
|Mozer
|2001
ASAL|<fbsym>FBal0124304==Dr<up>R10</up></fbsym>
CC|Selected as revertant of eye phenotype associated with
| <fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>; partial deletion of the <fbsym>FBgn0005384==3S18</fbsym> element.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136848
|Mozer
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018425	ICL 1 3S18	SYM 1 3S18{?'}Dr<up>R21</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Oct 2001	RESZ 547
ID|FBti0018425
SYM|3S18{?'}Dr<up>R21</up>
ASTP|<fbsym>FBtp0014767==3S18{?'}</fbsym>
DT|15 Oct 2001
|3 Oct 2001
ICL|3S18
PRG|<fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>
ASGN|<fbsym>FBgn0000492==Dr</fbsym>

REFDSR
{
RDID|FBrf0136848
|Mozer
|2001
ASAL|<fbsym>FBal0124303==Dr<up>R21</up></fbsym>
CC|Selected as revertant of eye phenotype associated with
| <fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>; partial deletion of the <fbsym>FBgn0005384==3S18</fbsym> element.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136848
|Mozer
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018426	ICL 1 3S18	SYM 1 3S18{?'}Dr<up>R22</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Oct 2001	RESZ 547
ID|FBti0018426
SYM|3S18{?'}Dr<up>R22</up>
ASTP|<fbsym>FBtp0014767==3S18{?'}</fbsym>
DT|15 Oct 2001
|3 Oct 2001
ICL|3S18
PRG|<fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>
ASGN|<fbsym>FBgn0000492==Dr</fbsym>

REFDSR
{
RDID|FBrf0136848
|Mozer
|2001
ASAL|<fbsym>FBal0124302==Dr<up>R22</up></fbsym>
CC|Selected as revertant of eye phenotype associated with
| <fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>; partial deletion of the <fbsym>FBgn0005384==3S18</fbsym> element.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136848
|Mozer
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018427	ICL 1 3S18	SYM 1 3S18{?'}Dr<up>R53</up>	ASTR 1 -	CLOC 1 -	REF 1 2	DT 1 15 Oct 2001	RESZ 547
ID|FBti0018427
SYM|3S18{?'}Dr<up>R53</up>
ASTP|<fbsym>FBtp0014767==3S18{?'}</fbsym>
DT|15 Oct 2001
|3 Oct 2001
ICL|3S18
PRG|<fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>
ASGN|<fbsym>FBgn0000492==Dr</fbsym>

REFDSR
{
RDID|FBrf0136848
|Mozer
|2001
ASAL|<fbsym>FBal0124301==Dr<up>R53</up></fbsym>
CC|Selected as revertant of eye phenotype associated with
| <fbsym>FBti0014114==3S18{}Dr<up>Mio</up></fbsym>; partial deletion of the <fbsym>FBgn0005384==3S18</fbsym> element.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136848
|Mozer
|2001
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019523	ICL 1 3S18	SYM 1 3S18{}4	ASTR 1 -	CLOC 1 1B2-1B2	REF 1 3	DT 1 21 Aug 2003	RESZ 518
ID|FBti0019523
SYM|3S18{}4
SYN|TE19523
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}4
CLOC|1B2-1B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003417.2
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|1B2-1B2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019554	ICL 1 3S18	SYM 1 3S18{}35	ASTR 1 -	CLOC 1 3D3-3D3	REF 1 3	DT 1 21 Aug 2003	RESZ 520
ID|FBti0019554
SYM|3S18{}35
SYN|TE19554
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}35
CLOC|3D3-3D3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003427.2
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|3D3-3D3
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019649	ICL 1 3S18	SYM 1 3S18{}177	ASTR 1 -	CLOC 1 19B1-19B1	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0019649
SYM|3S18{}177
SYN|TE19649
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}177
CLOC|19B1-19B1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002611.4
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|19B1-19B1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019655	ICL 1 3S18	SYM 1 3S18{}183	ASTR 1 -	CLOC 1 19C5-19C5	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0019655
SYM|3S18{}183
SYN|TE19655
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}183
CLOC|19C5-19C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003571.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|19C5-19C5
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018869	ICL 1 3S18	SYM 1 3S18{}853	ASTR 1 -	CLOC 1 55D4-55E1	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0018869
SYM|3S18{}853
SYN|TE18869
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}853
CLOC|55D4-55E1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003799.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|55D4-55E1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020201	ICL 1 3S18	SYM 1 3S18{}1090	ASTR 1 -	CLOC 1 79B3-79C1	REF 1 3	DT 1 21 Aug 2003	RESZ 528
ID|FBti0020201
SYM|3S18{}1090
SYN|TE20201
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|3S18

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|3S18{}1090
CLOC|79B3-79C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003596.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|79B3-79C1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0059931	ICL 1 3S18	SYM 1 3S18{}1870	ASTR 1 -	CLOC 1 80F7-80F7	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0059931
SYM|3S18{}1870
SYN|3S18#5775
|TE59931
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#5775
CLOC|80F7-80F7
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0060983	ICL 1 3S18	SYM 1 3S18{}2922	ASTR 1 -	CLOC 1 41D1-41D2	REF 1 2	DT 1 27 Apr 2005	RESZ 365
ID|FBti0060983
SYM|3S18{}2922
SYN|3S18#100189
|TE60983
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#100189
CLOC|41D1-41D2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0061050	ICL 1 3S18	SYM 1 3S18{}2989	ASTR 1 -	CLOC 1 80F9-80F9	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0061050
SYM|3S18{}2989
SYN|3S18#5973
|TE61050
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#5973
CLOC|80F9-80F9
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062015	ICL 1 3S18	SYM 1 3S18{}3954	ASTR 1 -	CLOC 1 64C6-64C6	REF 1 2	DT 1 27 Apr 2005	RESZ 365
ID|FBti0062015
SYM|3S18{}3954
SYN|3S18#100311
|TE62015
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#100311
CLOC|64C6-64C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062016	ICL 1 3S18	SYM 1 3S18{}3955	ASTR 1 -	CLOC 1 64C6-64C6	REF 1 2	DT 1 27 Apr 2005	RESZ 365
ID|FBti0062016
SYM|3S18{}3955
SYN|3S18#100312
|TE62016
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#100312
CLOC|64C6-64C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062017	ICL 1 3S18	SYM 1 3S18{}3956	ASTR 1 -	CLOC 1 64C6-64C6	REF 1 2	DT 1 27 Apr 2005	RESZ 365
ID|FBti0062017
SYM|3S18{}3956
SYN|3S18#100313
|TE62017
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#100313
CLOC|64C6-64C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062368	ICL 1 3S18	SYM 1 3S18{}4307	ASTR 1 -	CLOC 1 41B1-41B1	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0062368
SYM|3S18{}4307
SYN|3S18#1814
|TE62368
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#1814
CLOC|41B1-41B1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062480	ICL 1 3S18	SYM 1 3S18{}4419	ASTR 1 -	CLOC 1 20E2-20F1	REF 1 2	DT 1 27 Apr 2005	RESZ 363
ID|FBti0062480
SYM|3S18{}4419
SYN|3S18#10746
|TE62480
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#10746
CLOC|20E2-20F1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062881	ICL 1 3S18	SYM 1 3S18{}4820	ASTR 1 -	CLOC 1 18F2-18F2	REF 1 2	DT 1 27 Apr 2005	RESZ 363
ID|FBti0062881
SYM|3S18{}4820
SYN|3S18#10034
|TE62881
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#10034
CLOC|18F2-18F2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0063113	ICL 1 3S18	SYM 1 3S18{}5052	ASTR 1 -	CLOC 1 41F1-41F2	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0063113
SYM|3S18{}5052
SYN|3S18#2654
|TE63113
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#2654
CLOC|41F1-41F2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0063624	ICL 1 3S18	SYM 1 3S18{}5563	ASTR 1 -	CLOC 1 64C5-64C6	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0063624
SYM|3S18{}5563
SYN|3S18#4107
|TE63624
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|3S18

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|3S18#4107
CLOC|64C5-64C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014100	ICL 1 3S18	SYM 1 3S18{}Bx<up>J</up>	ASTR 1 -	CLOC 1 17C3--4	REF 1 2	DT 1 6 Jan 2000	RESZ 491
ID|FBti0014100
SYM|3S18{}Bx<up>J</up>
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|3S18
ASGN|<fbsym>FBgn0000242==Bx</fbsym>
SK|FBst0003997
|Bx[J]
|Total=1

REFDSR
{
RDID|FBrf0066905
|Lindsley and Zimm
|1992
SYN|3S18{}Bx<up>J</up>
ASAL|<fbsym>FBal0001441==Bx<up>J</up></fbsym>
MU|heat-treatment \?
CLOC|17C3--4
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000242==Bx</fbsym>
}

REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0001441==Bx<up>J</up></fbsym>

REFDSR
{
RDID|FBrf0028138
|Santamaria and Garcia-Bellido
|1975
PHP|Clonal analysis of wing disk development indicates massive cell loss
|during third larval instar. Clones of <fbsym>FBgn0000242==Bx</fbsym><up>+</up> cells in
| <fbsym>FBal0001441==Bx<up>J</up></fbsym>/+ wings that
|reach the margin but are confined to the dorsal or ventral surface often
|cause reconstitution of both surfaces and appearance of marginal elements
|derived from both surfaces.
PHM|dorsal mesothoracic disc
}

REFDSR
{
RDID|FBrf0033647
|Lifschytz and Green
|1979
PHP|The only dominant <fbsym>FBgn0000242==Bx</fbsym> allele not suppressed by a Bx deficiency or hdp.
}

REFDSR
{
RDID|FBrf0056217
|Jack and DeLotto
|1992
PHP|Homozygotes exhibit tissue loss from the entire wing margin and blistering
|of the wing blade. The phenotype is unchanged in double homozygote
|combinations with <fbsym>FBal0001938==ct<up>53d</up></fbsym>.
PHM|wing
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Wings reduced to slender strip; only posterior cell present at tip.
|Heterozygous females have half and homozygous females one third the normal
|number of cells in membrane of wing. Femur shortened or legs otherwise
|abnormal, especially third pair. Halteres abnormal. Interacts with <fbsym>FBgn0000179==bi</fbsym> to
|give more nearly normal wings.
|RK1.
PHM|wing
|haltere
|femur
}

REFDSR
{
RDID|FBrf0159703
|Chen et al.
|2002
PHM|wing
}

REFDSR
{
RDID|FBrf0180477
|Tsai et al.
|2004
PHP|Mutant animals exhibit an decreased sensitivity to cocaine. After exposure
|to 100ug of cocaine, control animals show a slow circling behavior
|and some are akinetic, mutant animals are much less affected, showing
|increased locomotion (mostly in straight lines) decreased slow circling,
|and almost no akinesia. Mutant animals, unlike controls which show
|very little movement, remain in motion at 125ug exposure showing circling
|behaviors.
}

REF
{
REFM|FBrf0028138
|Santamaria and Garcia-Bellido
|1975
REFM|FBrf0033647
|Lifschytz and Green
|1979
REFM|FBrf0056217
|Jack and DeLotto
|1992
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0159703
|Chen et al.
|2002
REFM|FBrf0180477
|Tsai et al.
|2004
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014114	ICL 1 3S18	SYM 1 3S18{}Dr<up>Mio</up>	ASTR 1 -	CLOC 1 99B3	REF 1 4	DT 1 6 Jan 2000	RESZ 1495
ID|FBti0014114
SYM|3S18{}Dr<up>Mio</up>
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|3S18
ASGN|<fbsym>FBgn0000492==Dr</fbsym>
SK|FBst0000007
|P{ry[+t7.2]=hsFLP}1, y[1] w[1118]; Dr[Mio]/TM3, ry[*] Sb[1]
|FBst0000406
|Dr[Mio]/TMS, P{ry[+t7.2]=Delta2-3}99B
|FBst0000491
|Dr[Mio]/TM6, Ubx[+]
|FBst0001189
|emc[D] st[1] in[1] kni[ri-1] p[p] Dr[Mio]/TM6C, ca[1]
|FBst0001255
|TM6B, <fbsym>FBal0003110==Dr[Mio]</fbsym> Tb[+]/Ubx[Cbx-1] Ubx[1] gl[3]
|FBst0001289
|C(1)M4, y[2]; TM6B, Tb[1] Dr[Mio]/In(3R)Dl[B], Dl[B]
|FBst0001290
|Df(3R)ca[nd1], e[s] ncd[1] ca[nd1]/In(3R)C, sprd[1] e[1] <fbsym>FBal0003110==Dr[Mio]</fbsym> ca[1]
|FBst0003167
|T(2;3)CyO-TM2, CyO, l(2)DTS513[1]: TM2/Dr[Mio]
|FBst0003218
|TM3, P{ry[+t7.2]=ftz-lacZ.ry[+]}TM3, Sb[1] ry[*]/Dr[Mio]
|FBst0003644
|TM3, Sb[1]/TM6B, Tb[1] <fbsym>FBal0003110==Dr[Mio]</fbsym>
|FBst0006663
|w[1118]; Dr[Mio]/TM3, P{w[+mC]=GAL4-twi.G}2.3, P{UAS-2xEGFP}AH2.3, Sb[1] Ser[1]
|Total=11

REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHC|lethal | recessive
}

REFDSR
{
RDID|FBrf0076958
|Tearle et al.
|1994
PHC|lethal | embryonic stage | recessive
}

REFDSR
{
RDID|FBrf0079057
|Mozer
|1995
SYN|3S18{}Dr<up>Mio</up>
ASAL|<fbsym>FBal0003110==Dr<up>Mio</up></fbsym>
MU|nitrogen mustard
CLOC|99B3
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000492==Dr</fbsym>
}

REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0076958
|Tearle et al.
|1994
REFM|FBrf0079057
|Mozer
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0003110==Dr<up>Mio</up></fbsym>

REFDSR
{
RDID|FBrf0049495
|Renfranz and Benzer
|1989
PHP|Adult eyes are very reduced and rough with about 30 facets. Some rhabdomeres
|within ommatidia are fused. Eye disc size is reduced.
}

REFDSR
{
RDID|FBrf0064498
|Heberlein et al.
|1993
PHP|The progression of the morphogenetic furrow in the developing eye disc
|arrests. The eye disc appears normal at the time of arrest. dpp expression
|is abolished (as assayed with a dpp-lacZ fusion gene).
}

REFDSR
{
RDID|FBrf0076958
|Tearle et al.
|1994
PHP|Severe disruption of eye development. Heterozygotes with
| <fbsym>FBal0003107==Dr<up>1</up></fbsym> are
|semi-lethal, 10-30% adults survive to eclosion, surviving adults exhibit
|reduced eye, deranged bristle pattern on the thorax, abdomen, legs
|and wing margins and locomotor defects so the flies could hardly move.
|A similar phenotype is seen when heterozygous with
| <fbsym>FBal0003107==Dr<up>1</up></fbsym> revertant
|alleles and <fbsym>FBgn0003525==stg</fbsym> alleles. Heterozygotes with <fbsym>FBal0003111==Wedge<up>1</up></fbsym>
| only exhibit
|the reduced eye phenotype. Interact in trans with lesions in <fbsym>FBgn0003525==stg</fbsym>
|... (see <fbsym>FBal0003110==Dr<up>Mio</up></fbsym> report)
PHM|macrochaeta
|eye
}

REFDSR
{
RDID|FBrf0083505
|Vosshall and Young
|1995
PHP|Mutants display locomotor activity rhythms with circadian periods,
|though with reduced penetrance (small sample size). Average period
|length of the locomotor activity is rather short.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|homozygous lethal
}

REFDSR
{
RDID|FBrf0136848
|Mozer
|2001
PHP|Heterozygotes have severely reduced eyes, containing less than 30 ommatidia.
|The shape of the mutant eye resembles an inverted drop. No patterning
|defects are seen in the retina.
|Five-cell preclusters are not seen in the heterozygous eye disc at
|the time when multiple rows of developing ommatidia are seen in wild-type
|discs, and instead a single row of mature ommatidial clusters is seen.
|Massive cell death associated with absence of furrow progression is
|... (see <fbsym>FBal0003110==Dr<up>Mio</up></fbsym> report)
PHM|eye
|ommatidium
|five-cell ommatidial precursor
}

REF
{
REFM|FBrf0049495
|Renfranz and Benzer
|1989
REFM|FBrf0064498
|Heberlein et al.
|1993
REFM|FBrf0076958
|Tearle et al.
|1994
REFM|FBrf0083505
|Vosshall and Young
|1995
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0136848
|Mozer
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014552	ICL 1 3S18	SYM 1 3S18{}nod<up>2</up>	ASTR 1 -	CLOC 1 10C8--9	REF 1 4	DT 1 6 Jan 2000	RESZ 745
ID|FBti0014552
SYM|3S18{}nod<up>2</up>
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|3S18
ASGN|<fbsym>FBgn0002948==nod</fbsym>
ABA|<fbsym>FBab0004160==In(1)nod-bd</fbsym>
SK|FBst0002324
|FM7a, In(1)nod-bd/y[1] w[a] ct[6] lz[1] v[1] f[1]/Dp(1;Y)y[+]; sv[spa-pol]
|FBst0002331
|FM7a, nod[2]/Dp(1;Y)y[+]/C(1)DX, y[1] f[1]; sv[spa-pol]
|Total=2

REFDSR
{
RDID|FBrf0051351
|Zhang et al.
|1990
SYN|3S18{}nod<up>2</up>
ASAL|<fbsym>FBal0013066==nod<up>2</up></fbsym>
MU|&ggr; ray
CLOC|10C8--9
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0002948==nod</fbsym>
}

REF
{
REFM|FBrf0051351
|Zhang et al.
|1990
REFM|FBrf0051920
|Zhang and Hawley
|1990
REFM|FBrf0055002
|Knowles and Hawley
|1991
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0013066==nod<up>2</up></fbsym>

REFDSR
{
RDID|FBrf0051920
|Zhang and Hawley
|1990
PHP|High levels of X and fourth chromosome nondisjunction.
}

REFDSR
{
RDID|FBrf0134637
|Apionishev et al.
|2001
PHP|<fbsym>FBal0013064==nod<up>a</up></fbsym>/<fbsym>FBba0000007==FM7a</fbsym>
| <fbsym>FBal0013066==nod<up>2</up></fbsym> females show 43% X chromosome nondisjunction
|and 89% 4th chromosome nondisjunction.
PHM|(with nod<up>a</up>) meiosis & nuclear chromosome | female
}

REF
{
REFM|FBrf0051920
|Zhang and Hawley
|1990
REFM|FBrf0134637
|Apionishev et al.
|2001
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0002823	ICL 1 3S18	SYM 1 3S18{}w<up>a4</up>	ASTR 1 -	CLOC 1 3B6	REF 1 13	DT 1 4 Feb 2000	RESZ 956
ID|FBti0002823
SYM|3S18{}w<up>a4</up>
SYN|BEL{}w<up>a4</up>
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|4 Feb 2000
|24 Jun 1997
ICL|3S18
ID2|FBti0002386
ASGN|<fbsym>FBgn0003996==w</fbsym>
SK|FBst0000152
|w[a4]
|Total=1

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
ASAL|<fbsym>FBal0018198==w<up>a4</up></fbsym>
MU|spontaneous
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
PHC|viable
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0050555
|Georgiev and Gerasimova
|1989
REFM|FBrf0051917
|Peng and Mount
|1990
REFM|FBrf0054158
|Rabinow et al.
|1991
REFM|FBrf0073744
|Lim and Simmons
|1994
REFM|FBrf0080401
|Soriano et al.
|1995
REFM|FBrf0081893
|Davis and Judd
|1995
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0086910
|Bhadra and Birchler
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0094159
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018198==w<up>a4</up></fbsym>

REFDSR
{
RDID|FBrf0037612
|Zachar and Bingham
|1982
PHP|Eye color: orange-brown.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0084258
|Peng and Mount
|1995
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: yellow-orange in male; lighter, yellower, in female; both
|sexes paler than <fbsym>FBal0018195==w<up>a</up></fbsym>.
|Malpighian tubule color: colorless.
PHM|pigment cell
|Malpighian tubule
}

REF
{
REFM|FBrf0037612
|Zachar and Bingham
|1982
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0084258
|Peng and Mount
|1995
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0014807	ICL 1 3S18	SYM 1 3S18{}w<up>zm</up>	ASTR 1 -	CLOC 1 3B6	REF 1 7	DT 1 6 Jan 2000	RESZ 662
ID|FBti0014807
SYM|3S18{}w<up>zm</up>
ASTP|<fbsym>FBtp0011408==3S18</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|3S18
ASGN|<fbsym>FBgn0003996==w</fbsym>

REFDSR
{
RDID|FBrf0049635
|Rabinow and Birchler
|1989
SYN|3S18{}w<up>zm</up>
ASAL|<fbsym>FBal0018326==w<up>zm</up></fbsym>
MU|spontaneous
|unequal recombination
CLOC|3B6
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003996==w</fbsym>
}

REF
{
REFM|FBrf0049635
|Rabinow and Birchler
|1989
REFM|FBrf0068635
|Peterson et al.
|1994
REFM|FBrf0081893
|Davis and Judd
|1995
REFM|FBrf0084074
|Judd
|1995
REFM|FBrf0087538
|Larsson et al.
|1996
REFM|FBrf0094158
|Bhadra et al.
|1997
REFM|FBrf0105495
|FlyBase
|1992-
}

ALESR
{
ASYM|<fbsym>FBal0018326==w<up>zm</up></fbsym>

REFDSR
{
RDID|FBrf0026500
|Kalisch and Rasmuson
|1974
PHP|In homozygous <fbsym>FBgn0004050==z</fbsym><up>+</up> female <fbsym>FBal0018326==w<up>zm</up></fbsym> causes
| variegation of the eye pigmentation.
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0049829
|Birchler et al.
|1989
PHM|pigment cell
}

REFDSR
{
RDID|FBrf0076540
|Csink et al.
|1994
PHP|No interaction with mutations of <fbsym>FBgn0003261==Rm62</fbsym>.
}

REFDSR
{
RDID|FBrf0084074
|Judd
|1995
PHP|Eye color: wild-type, in <fbsym>FBgn0004050==z</fbsym><up>+</up> males or females.
|Eye color: red-brown mottled, in <fbsym>FBal0018822==z<up>1</up></fbsym> male.
|Eye color: occasional red mottling, in <fbsym>FBal0018822==z<up>1</up></fbsym> female.
|Eye color: lighter yellow background as <fbsym>FBal0018848==z<up>v77h</up></fbsym>
| <fbsym>FBal0018325==w<up>zl</up></fbsym> male, compared with <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018325==w<up>zl</up></fbsym> male.
|Eye color: darker yellow than <fbsym>FBal0018822==z<up>1</up></fbsym> as
| <fbsym>FBal0018848==z<up>v77h</up></fbsym> <fbsym>FBal0018325==w<up>zl</up></fbsym> female.
}

REFDSR
{
RDID|FBrf0094184
|Birve and Rasmuson-Lestander
|1994
PHP|Repression of <fbsym>FBal0018326==w<up>zm</up></fbsym> by <fbsym>FBal0018822==z<up>1</up></fbsym> is
| suppressed by <fbsym>FBal0063038==Su(z)12<up>1</up></fbsym>.
}

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Eye color: wild-type in <fbsym>FBgn0004050==z</fbsym><up>+</up> <fbsym>FBal0018326==w<up>zm</up></fbsym> male and
| <fbsym>FBgn0004050==z</fbsym><up>+</up> <fbsym>FBal0018326==w<up>zm</up></fbsym>/<fbsym>FBgn0004050==z</fbsym><up>+</up>
| <fbsym>FBal0018326==w<up>zm</up></fbsym> female.
|Eye color: lemon yellow, in <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018326==w<up>zm</up></fbsym> female at 25<up>o</up>-30<up>o</up>C.
|Eye color: orange with red spots, in <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018326==w<up>zm</up></fbsym> female at 14<up>o</up>C.
|Eye color: lemon yellow with fine-grained red spots, in
| <fbsym>FBal0018822==z<up>1</up></fbsym> <fbsym>FBal0018326==w<up>zm</up></fbsym> male at 25<up>o</up>C-30<up>o</up>C.
|Eye color: almost wild-type, in <fbsym>FBal0018822==z<up>1</up></fbsym>
| <fbsym>FBal0018326==w<up>zm</up></fbsym> male at 14<up>o</up>C-17<up>o</up>C.
|Eye color: mottled, with <fbsym>FBgn0002910==mw</fbsym>.
}

REF
{
REFM|FBrf0026500
|Kalisch and Rasmuson
|1974
REFM|FBrf0049829
|Birchler et al.
|1989
REFM|FBrf0076540
|Csink et al.
|1994
REFM|FBrf0084074
|Judd
|1995
REFM|FBrf0094184
|Birve and Rasmuson-Lestander
|1994
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0013011	ICL 1 17.6	SYM 1 17.6{?'LTR}Cyp6a2<up>91C</up>	ASTR 1 -	CLOC 1 42D1	REF 1 3	DT 1 14 Sep 1999	RESZ 549
ID|FBti0013011
SYM|17.6{?'LTR}Cyp6a2<up>91C</up>
SYN|17.6{?'LTR}Cyp6a2<up>91C</up>
ASTP|<fbsym>FBtp0002766==17.6{?'LTR}</fbsym>
DT|14 Sep 1999
|14 Sep 1999
ICL|17.6
ASGN|<fbsym>FBgn0000473==Cyp6a2</fbsym>

REFDSR
{
RDID|FBrf0057534
|Waters et al.
|1992
SYN|17.6{?'LTR}Cyp6a2<up>91C</up>
ASAL|<fbsym>FBal0002207==Cyp6a2<up>91C</up></fbsym>
CLOC|42D1
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0000473==Cyp6a2</fbsym>
}

REF
{
REFM|FBrf0057534
|Waters et al.
|1992
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0105973
|Dombrowski et al.
|1998
}

ALESR
{
ASYM|<fbsym>FBal0002207==Cyp6a2<up>91C</up></fbsym>

REFDSR
{
RDID|FBrf0105495
|FlyBase
|1992-
PHP|Characteristic of insecticide susceptible strains.
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EO ALESR

}

# EOR

TIR
{

RETE|ID 1 FBti0019563	ICL 1 17.6	SYM 1 17.6{}44	ASTR 1 -	CLOC 1 3E8-3E8	REF 1 3	DT 1 21 Aug 2003	RESZ 520
ID|FBti0019563
SYM|17.6{}44
SYN|TE19563
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}44
CLOC|3E8-3E8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003428.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|3E8-3E8
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019053	ICL 1 17.6	SYM 1 17.6{}125	ASTR 1 -	CLOC 1 12E8-12E8	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0019053
SYM|17.6{}125
SYN|TE19053
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}125
CLOC|12E8-12E8
LOCB|genomic location inferred from flanking sequence
DBAF|AE003495.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|12E8-12E8
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018861	ICL 1 17.6	SYM 1 17.6{}790	ASTR 1 -	CLOC 1 46B2-46B2	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0018861
SYM|17.6{}790
SYN|TE18861
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}790
CLOC|46B2-46B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003832.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|46B2-46B2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0018862	ICL 1 17.6	SYM 1 17.6{}804	ASTR 1 -	CLOC 1 47C7-47C7	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0018862
SYM|17.6{}804
SYN|TE18862
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}804
CLOC|47C7-47C7
LOCB|genomic location inferred from flanking sequence
DBAF|AE003827.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|47C7-47C7
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020019	ICL 1 17.6	SYM 1 17.6{}908	ASTR 1 -	CLOC 1 62A3-62A3	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0020019
SYM|17.6{}908
SYN|TE20019
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}908
CLOC|62A3-62A3
LOCB|genomic location inferred from flanking sequence
DBAF|AE003471.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|62A3-62A3
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020086	ICL 1 17.6	SYM 1 17.6{}975	ASTR 1 -	CLOC 1 67D5-67D5	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0020086
SYM|17.6{}975
SYN|TE20086
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}975
CLOC|67D5-67D5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003550.4
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|67D5-67D5
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020090	ICL 1 17.6	SYM 1 17.6{}979	ASTR 1 -	CLOC 1 68C1-68C1	REF 1 3	DT 1 21 Aug 2003	RESZ 526
ID|FBti0020090
SYM|17.6{}979
SYN|TE20090
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}979
CLOC|68C1-68C1
LOCB|genomic location inferred from flanking sequence
DBAF|AE003545.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|68C1-68C1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020174	ICL 1 17.6	SYM 1 17.6{}1063	ASTR 1 -	CLOC 1 77B4-77B4	REF 1 3	DT 1 21 Aug 2003	RESZ 528
ID|FBti0020174
SYM|17.6{}1063
SYN|TE20174
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}1063
CLOC|77B4-77B4
LOCB|genomic location inferred from flanking sequence
DBAF|AE003591.4
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|77B4-77B4
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0020227	ICL 1 17.6	SYM 1 17.6{}1116	ASTR 1 -	CLOC 1 80C5-80D1	REF 1 3	DT 1 21 Aug 2003	RESZ 528
ID|FBti0020227
SYM|17.6{}1116
SYN|TE20227
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}1116
CLOC|80C5-80D1
LOCB|genomic location inferred from flanking sequence
DBAF|AE002786.2
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|80C5-80D1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019299	ICL 1 17.6	SYM 1 17.6{}1213	ASTR 1 -	CLOC 1 82E5-82E5	REF 1 3	DT 1 21 Aug 2003	RESZ 528
ID|FBti0019299
SYM|17.6{}1213
SYN|TE19299
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}1213
CLOC|82E5-82E5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003604.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|82E5-82E5
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019354	ICL 1 17.6	SYM 1 17.6{}1287	ASTR 1 -	CLOC 1 86C6-86C6	REF 1 3	DT 1 21 Aug 2003	RESZ 528
ID|FBti0019354
SYM|17.6{}1287
SYN|TE19354
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|17.6

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|17.6{}1287
CLOC|86C6-86C6
LOCB|genomic location inferred from flanking sequence
DBAF|AE003688.2
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|86C6-86C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0059975	ICL 1 17.6	SYM 1 17.6{}1914	ASTR 1 -	CLOC 1 41C6-41C6	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0059975
SYM|17.6{}1914
SYN|17.6#2108
|TE59975
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#2108
CLOC|41C6-41C6
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0060121	ICL 1 17.6	SYM 1 17.6{}2060	ASTR 1 -	CLOC 1 40F4-40F4	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0060121
SYM|17.6{}2060
SYN|17.6#1452
|TE60121
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#1452
CLOC|40F4-40F4
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0060473	ICL 1 17.6	SYM 1 17.6{}2412	ASTR 1 -	CLOC 1 20A2-20A3	REF 1 2	DT 1 27 Apr 2005	RESZ 365
ID|FBti0060473
SYM|17.6{}2412
SYN|17.6#100803
|TE60473
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#100803
CLOC|20A2-20A3
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0060705	ICL 1 17.6	SYM 1 17.6{}2644	ASTR 1 -	CLOC 1 40F7-40F7	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0060705
SYM|17.6{}2644
SYN|17.6#1582
|TE60705
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#1582
CLOC|40F7-40F7
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0060995	ICL 1 17.6	SYM 1 17.6{}2934	ASTR 1 -	CLOC 1 80F9-80F9	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0060995
SYM|17.6{}2934
SYN|17.6#5920
|TE60995
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#5920
CLOC|80F9-80F9
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0061074	ICL 1 17.6	SYM 1 17.6{}3013	ASTR 1 -	CLOC 1 80F9-80F9	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0061074
SYM|17.6{}3013
SYN|17.6#5992
|TE61074
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#5992
CLOC|80F9-80F9
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0062476	ICL 1 17.6	SYM 1 17.6{}4415	ASTR 1 -	CLOC 1 20F1-20F1	REF 1 2	DT 1 27 Apr 2005	RESZ 363
ID|FBti0062476
SYM|17.6{}4415
SYN|17.6#10742
|TE62476
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#10742
CLOC|20F1-20F1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0063581	ICL 1 17.6	SYM 1 17.6{}5520	ASTR 1 -	CLOC 1 39F1-39F1	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0063581
SYM|17.6{}5520
SYN|17.6#1252
|TE63581
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#1252
CLOC|39F1-39F1
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0064268	ICL 1 17.6	SYM 1 17.6{}6207	ASTR 1 -	CLOC 1 42A2-42A2	REF 1 2	DT 1 27 Apr 2005	RESZ 361
ID|FBti0064268
SYM|17.6{}6207
SYN|17.6#2810
|TE64268
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|27 Apr 2005
|27 Apr 2005
ICL|17.6

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
SYN|17.6#2810
CLOC|42A2-42A2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0014701	ICL 1 17.6	SYM 1 17.6{}su(s)<up>29</up>	ASTR 1 -	CLOC 1 1B13	REF 1 2	DT 1 6 Jan 2000	RESZ 465
ID|FBti0014701
SYM|17.6{}su(s)<up>29</up>
ASTP|<fbsym>FBtp0011399==17.6</fbsym>
DT|6 Jan 2000
|6 Jan 2000
ICL|17.6
ASGN|<fbsym>FBgn0003575==su(s)</fbsym>
ARGS|FBgn0003575

REFDSR
{
RDID|FBrf0051918
|Voelker et al.
|1990
SYN|17.6{}su(s)<up>29</up>
ASAL|<fbsym>FBal0016372==su(s)<up>29</up></fbsym>
CLOC|1B13
|Insertion site 
LOCB|Proximity to gene: <fbsym>FBgn0003575==su(s)</fbsym>
}

REF
{
REFM|FBrf0051918
|Voelker et al.
|1990
REFM|FBrf0105495
|FlyBase
|1992-
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019525	ICL 1 297	SYM 1 297{}6	ASTR 1 -	CLOC 1 1C5-1C5	REF 1 3	DT 1 21 Aug 2003	RESZ 514
ID|FBti0019525
SYM|297{}6
SYN|TE19525
ASTP|<fbsym>FBtp0011407==297</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|297

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|297{}6
CLOC|1C5-1C5
LOCB|genomic location inferred from flanking sequence
DBAF|AE003418.2
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|1C5-1C5
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019567	ICL 1 297	SYM 1 297{}48	ASTR 1 -	CLOC 1 4B2-4B2	REF 1 3	DT 1 21 Aug 2003	RESZ 516
ID|FBti0019567
SYM|297{}48
SYN|TE19567
ASTP|<fbsym>FBtp0011407==297</fbsym>
DT|21 Aug 2003
|21 Aug 2003
ICL|297

REFDSR
{
RDID|FBrf0155828
|Kaminker et al.
|2002
SYN|297{}48
CLOC|4B2-4B2
LOCB|genomic location inferred from flanking sequence
DBAF|AE003430.3
}

REFDSR
{
RDID|FBrf0184336
|Quesneville et al.
|2005.6.22
CLOC|4B2-4B2
LOCB|genomic location inferred from flanking sequence
}

REF
{
REFM|FBrf0105495
|FlyBase
|1992-
REFM|FBrf0155828
|Kaminker et al.
|2002
REFM|FBrf0184336
|Quesneville et al.
|2005.6.22
}

}

# EOR

TIR
{

RETE|ID 1 FBti0019580	ICL