ABSR
{
RETE|ID 1 FBab0025194	CLA 1 Aberration	GSYM 1 Ab(?)B13	DT 1 08 Nov 97	RESZ 364	REF 1	
ABSY|Ab(?)B13
DT|08 Nov 97
SYN|R(B)13
ID|FBab0025194
REF
{
REFM|FBrf0088157
|Goldsborough and Kornberg
|1996
|0
}

REFDSR
{
RDID|FBrf0088157
|Goldsborough and Kornberg
|1996
OTH|Induced on the Brasil wild type chromosome.
PHP|Moderately suppresses transvection in @Ubx<up>1:Cbx-1</up>@/+ heterozygotes.
SYN|R(B)13
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0025195	CLA 1 Aberration	GSYM 1 Ab(?)B3	DT 1 08 Nov 97	RESZ 359	REF 1	
ABSY|Ab(?)B3
DT|08 Nov 97
SYN|R(B)3
ID|FBab0025195
REF
{
REFM|FBrf0088157
|Goldsborough and Kornberg
|1996
|-1
}

REFDSR
{
RDID|FBrf0088157
|Goldsborough and Kornberg
|1996
OTH|Induced on the Brasil wild type chromosome.
PHP|Strongly suppresses transvection in @Ubx<up>1:Cbx-1</up>@/+ heterozygotes.
SYN|R(B)3
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0025196	CLA 1 Aberration	GSYM 1 Ab(?)B4	DT 1 08 Nov 97	RESZ 357	REF 1	
ABSY|Ab(?)B4
DT|08 Nov 97
SYN|R(B)4
ID|FBab0025196
REF
{
REFM|FBrf0088157
|Goldsborough and Kornberg
|1996
|-1
}

REFDSR
{
RDID|FBrf0088157
|Goldsborough and Kornberg
|1996
OTH|Induced on the Brasil wild type chromosome.
PHP|Weakly suppresses transvection in @Ubx<up>1:Cbx-1</up>@/+ heterozygotes.
SYN|R(B)4
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0025197	CLA 1 Aberration	GSYM 1 Ab(?)B8	DT 1 08 Nov 97	RESZ 357	REF 1	
ABSY|Ab(?)B8
DT|08 Nov 97
SYN|R(B)8
ID|FBab0025197
REF
{
REFM|FBrf0088157
|Goldsborough and Kornberg
|1996
|-1
}

REFDSR
{
RDID|FBrf0088157
|Goldsborough and Kornberg
|1996
OTH|Induced on the Brasil wild type chromosome.
PHP|Weakly suppresses transvection in @Ubx<up>1:Cbx-1</up>@/+ heterozygotes.
SYN|R(B)8
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029530	CLA 1 Aberration	GSYM 1 Ab(?)DTD44.2	DT 1 03 Jun 01	RESZ 705	REF 1	
ABSY|Ab(?)DTD44.2
DT|03 Jun 01
SYN|DTDD44.2
ID|FBab0029530
REF
{
REFM|FBrf0132343
|Su et al.
|2001
|-1
}

MU|irradiation
COR|Selected as: an exceptional DTD (dpp transvection disruptor) that results in heldout wings in combination with @dpp<up>d-ho</up>@/@dpp<up>hr4</up>@.
|Induced on: a @dpp<up>d-ho</up>@ chromosome.
CCM|Complex cytology.
REFDSR
{
RDID|FBrf0132343
|Su et al.
|2001
MU|irradiation
COR|Selected as: an exceptional DTD (dpp transvection disruptor) that results in heldout wings in combination with @dpp<up>d-ho</up>@/@dpp<up>hr4</up>@.
|Induced on: a @dpp<up>d-ho</up>@ chromosome.
CCM|Complex cytology.
PHP|Homozygous lethal.
SYN|DTDD44.2
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029531	CLA 1 Aberration	GSYM 1 Ab(?)DTD45.2	DT 1 03 Jun 01	RESZ 935	REF 1	
ABSY|Ab(?)DTD45.2
DT|03 Jun 01
SYN|DTD45.2
ID|FBab0029531
REF
{
REFM|FBrf0132343
|Su et al.
|2001
|-1
}

MU|irradiation
COR|Selected as: an exceptional DTD (dpp transvection disruptor) that results in heldout wings in combination with @dpp<up>d-ho</up>@/@dpp<up>hr4</up>@.
|Induced on: a @dpp<up>d-ho</up>@ chromosome.
CCM|Complex cytology. No females carrying @Ab(?)DTD45.2@ are observed
|possibly due to an undetected translocation between chromosomes 2 and
|Y.
REFDSR
{
RDID|FBrf0132343
|Su et al.
|2001
MU|irradiation
COR|Selected as: an exceptional DTD (dpp transvection disruptor) that results in heldout wings in combination with @dpp<up>d-ho</up>@/@dpp<up>hr4</up>@.
|Induced on: a @dpp<up>d-ho</up>@ chromosome.
CCM|Complex cytology. No females carrying @Ab(?)DTD45.2@ are observed
|possibly due to an undetected translocation between chromosomes 2 and
|Y.
SYN|DTD45.2
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028197	CLA 1 Aberration	GSYM 1 Ab(?;3)TSR-2<up>Sz</up>	DT 1 31 Aug 01	RESZ 836	CLOC 1 [];87B	REF 1	
ABSY|Ab(?;3)TSR-2<up>Sz</up>
DT|31 Aug 01
SYN|TSR-2<up>Sz</up>
ID|FBab0028197
REF
{
REFM|FBrf0103039
|Sipos et al.
|1998
|-1
}

BPT|[];87B
CCM|All limits from polytene analysis (FBrf0103039)
MU|X ray
COR|Induced on: an @Abd-B<up>Fab7-1</up>@ chromosome.
|Selected as: a mutation on an @Abd-B<up>Fab7-1</up>@ chromosome that eliminates or reduces the suppression of the @Abd-B<up>Fab7-1</up>@ gain of function phenotype by @Abd-B<up>iab8-D16</up>@.
REFDSR
{
RDID|FBrf0103039
|Sipos et al.
|1998
BPT|het;87B
MU|X ray
COR|Induced on: an @Abd-B<up>Fab7-1</up>@ chromosome.
|Selected as: a mutation on an @Abd-B<up>Fab7-1</up>@ chromosome that eliminates or reduces the suppression of the @Abd-B<up>Fab7-1</up>@ gain of function phenotype by @Abd-B<up>iab8-D16</up>@.
SYN|TSR-2<up>Sz</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029777	CLA 1 Aberration	GSYM 1 Ab(?;f)A887	DT 1 01 Apr 03	RESZ 350	REF 1	
ABSY|Ab(?;f)A887
DT|01 Apr 03
SYN|A887
ID|FBab0029777
REF
{
REFM|FBrf0149015
|Yan et al.
|2002
|-1
}

REFDSR
{
RDID|FBrf0149015
|Yan et al.
|2002
TRNA|FBti0023924 == P{SUPor-P}A887
OTH|@P{SUPor-P}A887@ is inserted in the centric region of @Ab(?;f)A887@,
|which appears to be a minichromosome.
SYN|A887
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029751	CLA 1 Aberration	GSYM 1 Ab(1)r20	DT 1 17 Jul 02	RESZ 227	REF 1	
ABSY|Ab(1)r20
DT|17 Jul 02
SYN|r20
ID|FBab0029751
REF
{
REFM|FBrf0144905
|Popkova et al.
|2001
|-1
}

REFDSR
{
RDID|FBrf0144905
|Popkova et al.
|2001
SYN|r20
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028195	CLA 1 Aberration	GSYM 1 Ab(1)w<up>8x1</up>N<up>+</up>	DT 1 12 Nov 00	RESZ 940	REF 1	
ABSY|Ab(1)w<up>8x1</up>N<up>+</up>
DT|12 Nov 00
SYN|unnamed
ID|FBab0028195
REF
{
REFM|FBrf0042381
|Grimwade et al.
|1985
|-1
}

ASAL|FBal0091689 == N<up>66h26rv1</up>
|FBal0018079 == w<up>8x1</up>
BIP|3C2;3C7 (from In(1)N<up>66h26</up>)
MU|spontaneous
PRG|N<up>66h26</up>
|w<up>8x</up>
|In(1)N<up>66h26</up>
CCM|Cytologically normal in the 3C7 region, although some undefined abnormalities
|are seen in the 3C1-3C2 region. Reinversion of @In(1)N<up>66h26</up>@.
AMD|w
REFDSR
{
RDID|FBrf0042381
|Grimwade et al.
|1985
MU|spontaneous
PRG|N<up>66h26</up>
|w<up>8x</up>
|In(1)N<up>66h26</up>
CCM|Cytologically normal in the 3C7 region, although some undefined abnormalities
|are seen in the 3C1-3C2 region. Reinversion of @In(1)N<up>66h26</up>@.
AMD|w
OTH|Unstable in crosses involving a @w<up>a</up>@ @N<up>fa-g</up>@ @rb<up>1</up>@ stock.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028196	CLA 1 Aberration	GSYM 1 Ab(1)w<up>8x2</up>N<up>+</up>	DT 1 12 Nov 00	RESZ 852	REF 1	
ABSY|Ab(1)w<up>8x2</up>N<up>+</up>
DT|12 Nov 00
SYN|unnamed
ID|FBab0028196
REF
{
REFM|FBrf0042381
|Grimwade et al.
|1985
|-1
}

ASAL|FBal0091688 == N<up>66h26rv2</up>
|FBal0018080 == w<up>8x2</up>
BIP|3C2;3C7 (from In(1)N<up>66h26</up>)
MU|spontaneous
PRG|N<up>66h26</up>
|w<up>8x</up>
|In(1)N<up>66h26</up>
CCM|Cytologically normal in the 3C7 region, although some undefined abnormalities
|are seen in the 3C1-3C2 region. Reinversion of @In(1)N<up>66h26</up>@.
AMD|w
REFDSR
{
RDID|FBrf0042381
|Grimwade et al.
|1985
MU|spontaneous
PRG|N<up>66h26</up>
|w<up>8x</up>
|In(1)N<up>66h26</up>
CCM|Cytologically normal in the 3C7 region, although some undefined abnormalities
|are seen in the 3C1-3C2 region. Reinversion of @In(1)N<up>66h26</up>@.
AMD|w
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027942	CLA 1 Aberration	GSYM 1 Ab(1)ZWD16	DT 1 22 Aug 04	RESZ 572	REF 1	
ABSY|Ab(1)ZWD16
DT|22 Aug 04
ID|FBab0027942
REF
{
REFM|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
|-1
}

MU|&ggr; ray
CCM|Class I rearrangement: breakpoints are between @w@ and the constriction.
|Breakpoints were not analyzed by in situ hybridization.
REFDSR
{
RDID|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
MU|&ggr; ray
CCM|Class I rearrangement: breakpoints are between @w@ and the constriction.
|Breakpoints were not analyzed by in situ hybridization.
PHP|Hemizygous males are wild type, homozygous males are sterile.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027943	CLA 1 Aberration	GSYM 1 Ab(1)ZWD17	DT 1 22 Aug 04	RESZ 572	REF 1	
ABSY|Ab(1)ZWD17
DT|22 Aug 04
ID|FBab0027943
REF
{
REFM|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
|-1
}

MU|&ggr; ray
CCM|Class I rearrangement: breakpoints are between @w@ and the constriction.
|Breakpoints were not analyzed by in situ hybridization.
REFDSR
{
RDID|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
MU|&ggr; ray
CCM|Class I rearrangement: breakpoints are between @w@ and the constriction.
|Breakpoints were not analyzed by in situ hybridization.
PHP|Hemizygous males are wild type, homozygous males are sterile.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023382	CLA 1 Aberration	GSYM 1 Ab(1;?)if<up>B2.1</up>	DT 1 29 Oct 99	RESZ 311	REF 1	
ABSY|Ab(1;?)if<up>B2.1</up>
DT|29 Oct 99
ID|FBab0023382
REF
{
REFM|FBrf0072704
|Brown
|1994
|-1
}

ASAL|FBal0039416 == if<up>B2.1</up>
MU|&ggr; ray
AMD|if
REFDSR
{
RDID|FBrf0072704
|Brown
|1994
MU|&ggr; ray
AMD|if
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023371	CLA 1 Aberration	GSYM 1 Ab(1;?)w<up>m4000</up>	DT 1 16 Jun 98	RESZ 420	REF 1	
ABSY|Ab(1;?)w<up>m4000</up>
DT|16 Jun 98
SYN|w<up>m4000</up>
ID2|FBal0018282
ID|FBab0023371
REF
{
REFM|FBrf0006058
|Buzzati-Traverso
|1943
|-1
}

DIS|Buzzati-Traverso, 7th Dec. 1941.
MU|X ray
CCM|rearrangement with break in w
PED|position-effect variegation for: w
PHP|eyes cream colored, darker in males
|male viable
|male fertile
|female viable
|female fertile
}
# EOR
ABSR
{
RETE|ID 1 FBab0028377	CLA 1 Aberration	GSYM 1 Ab(1;2)vs<up>P4</up>	DT 1 29 Oct 99	RESZ 491	REF 1	
ABSY|Ab(1;2)vs<up>P4</up>
DT|29 Oct 99
SYN|unnamed
ID|FBab0028377
REF
{
REFM|FBrf0063296
|Bateman
|1951
|-1
}

ASAL|FBal0092451 == vs<up>P4</up>
MU|<up>32</up>P
CCM|Segmental interchange involving the left end of the X chromosome and
|most of 2L.
AMD|vs
REFDSR
{
RDID|FBrf0063296
|Bateman
|1951
MU|<up>32</up>P
CCM|Segmental interchange involving the left end of the X chromosome and
|most of 2L.
AMD|vs
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024294	CLA 1 Aberration	GSYM 1 Ab(1;f)&ggr;845	DT 1 29 Oct 99	RESZ 687	REF 1	
ABSY|Ab(1;f)&ggr;845
DT|29 Oct 99
SYN|&ggr;845
ID|FBab0024294
REF
{
REFM|FBrf0084112
|Le et al.
|1995
|-1
}

ASAL|FBal0046835 == y<up>&ggr;845</up>
MU|&ggr; ray
PRG|Dp1187-8-23
CCM|Complex rearrangement on the @Dp(1;f)1187@ derivative @Dp1187-8-23@.
|Maybe a translocation + inversion, translocation + insertion or insertion
|+ inversion.
AMD|y
REFDSR
{
RDID|FBrf0084112
|Le et al.
|1995
MU|&ggr; ray
PRG|Dp1187-8-23
CCM|Complex rearrangement on the @Dp(1;f)1187@ derivative @Dp1187-8-23@.
|Maybe a translocation + inversion, translocation + insertion or insertion
|+ inversion.
AMD|y
SYN|&ggr;845
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027545	CLA 1 Aberration	GSYM 1 Ab(2)12-4	DT 1 29 Apr 01	RESZ 455	CLOC 1 49C	REF 1	
ABSY|Ab(2)12-4
DT|29 Apr 01
SYN|unnamed
ID|FBab0027545
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
}

BPT|49C
CCM|All limits from polytene analysis (FBrf0099191)
MU|X ray
PRG|FBti0016764 == P{lacW}50C.x3
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
BPT|49C;het
MU|X ray
PRG|FBti0016764 == P{lacW}50C.x3
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x3@.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027546	CLA 1 Aberration	GSYM 1 Ab(2)12-7	DT 1 29 Apr 01	RESZ 455	CLOC 1 46B	REF 1	
ABSY|Ab(2)12-7
DT|29 Apr 01
SYN|unnamed
ID|FBab0027546
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
}

BPT|46B
CCM|All limits from polytene analysis (FBrf0099191)
MU|X ray
PRG|FBti0016764 == P{lacW}50C.x3
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
BPT|46B;het
MU|X ray
PRG|FBti0016764 == P{lacW}50C.x3
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x3@.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027946	CLA 1 Aberration	GSYM 1 Ab(2)bw-R68	DT 1 16 Jun 98	RESZ 351	REF 1	
ABSY|Ab(2)bw-R68
DT|16 Jun 98
SYN|R<up>68</up>(+)
ID|FBab0027946
REF
{
REFM|FBrf0010226
|Slatis
|1955
|-1
}

MU|X ray
CCM|Complex rearrangement
REFDSR
{
RDID|FBrf0010226
|Slatis
|1955
MU|X ray
CCM|Complex rearrangement
PHP|Chromosome exhibits position effect variegation for @bw@: white eyes.
SYN|R<up>68</up>(+)
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027944	CLA 1 Aberration	GSYM 1 Ab(2)DTD117	DT 1 16 Nov 01	RESZ 408	REF 1	
ABSY|Ab(2)DTD117
DT|16 Nov 01
SYN|Decapentaplegic Transvection Disrupter rearrangement 117
ID|FBab0027944
REF
{
REFM|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
|-1
}

MU|&ggr; ray
CCM|Normal.
REFDSR
{
RDID|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
MU|&ggr; ray
CCM|Normal.
PHP|@z@ disrupted phenotype.
SYN|Decapentaplegic Transvection Disrupter rearrangement 117
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027945	CLA 1 Aberration	GSYM 1 Ab(2)DTD119	DT 1 16 Nov 01	RESZ 408	REF 1	
ABSY|Ab(2)DTD119
DT|16 Nov 01
SYN|Decapentaplegic Transvection Disrupter rearrangement 119
ID|FBab0027945
REF
{
REFM|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
|-1
}

MU|&ggr; ray
CCM|Normal.
REFDSR
{
RDID|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
MU|&ggr; ray
CCM|Normal.
PHP|@z@ disrupted phenotype.
SYN|Decapentaplegic Transvection Disrupter rearrangement 119
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029776	CLA 1 Aberration	GSYM 1 Ab(2)l(2)44Fp<up>9</up>	DT 1 26 Aug 02	RESZ 647	REF 1	
ABSY|Ab(2)l(2)44Fp<up>9</up>
DT|26 Aug 02
SYN|unnamed
ID|FBab0029776
REF
{
REFM|FBrf0147061
|Mohr and Boswell
|2002
|-1
}

ASAL|FBal0137186 == l(2)44Fp<up>9</up>
MU|ethyl methanesulfonate
AMD|l(2)44Fp
|l(2)44Fa
|l(2)44Fg
|l(2)44Fh
|l(2)44Fj
REFDSR
{
RDID|FBrf0147061
|Mohr and Boswell
|2002
MU|ethyl methanesulfonate
AMD|l(2)44Fp
|l(2)44Fa
|l(2)44Fg
|l(2)44Fh
|l(2)44Fj
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0037631	CLA 1 Aberration	GSYM 1 Ab(2)Pvr<up>KO8</up>	DT 1 29 Feb 04	RESZ 657	REF 1	
ABSY|Ab(2)Pvr<up>KO8</up>
DT|29 Feb 04
SYN|Pvr<up>KO8</up>
ID|FBab0037631
REF
{
REFM|FBrf0160936
|Sears et al.
|2003
|-1
}

MU|recombination
|SCEI endonuclease
|FLPase
PRG|Pvr<up>4.5.Scer\SceI.RS</up>
REFDSR
{
RDID|FBrf0160936
|Sears et al.
|2003
MU|recombination
|SCEI endonuclease
|FLPase
PRG|Pvr<up>4.5.Scer\SceI.RS</up>
OTH|Targeted homologous recombination event at the @Pvr@ locus, using @P{FRT(w<up>+</up>.Pvr<up>4.5.Scer\SceI.RS</up>)}@
|as the donor template. The chromosome appears to have undergone a
|complex combination of DNA insertion and duplication.
SYN|Pvr<up>KO8</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028056	CLA 1 Deficiency (cytologically invisible)	GSYM 1 Ab(2)Sco<up>rv15</up>	DT 1 12 Nov 00	RESZ 753	CLOC 1 [35B2];[35D1]	REF 1	
ABSY|Ab(2)Sco<up>rv15</up>
DT|12 Nov 00
SYN|unnamed
ID|FBab0028056
REF
{
REFM|FBrf0063478
|Grau et al.
|1984
|-1
}

ASAL|FBal0013053 == noc<up>Sco-rv15</up>
|FBal0088619 == sna<up>Sco-rv15</up>
BPT|[35B2];[35D1]
CCM|Limits of break 1 from complementation mapping against noc (FBrf0063478)
|Limits of break 2 from complementation mapping against sna (FBrf0063478)
FGD|bk1 hits noc << bk2 hits sna
BIP|35B1;35B3;35C1;35D1--2 (from Tp(2;2)Sco)
ACLA|Deficiency (cytologically invisible)
MU|ethyl methanesulfonate
PRG|Tp(2;2)Sco
AMD|sna
REFDSR
{
RDID|FBrf0063478
|Grau et al.
|1984
ACLA|Deficiency (cytologically invisible)
MU|ethyl methanesulfonate
PRG|Tp(2;2)Sco
AMD|sna
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024094	CLA 1 Aberration	GSYM 1 Ab(2)SM6#16	DT 1 28 Jan 02	RESZ 551	ALESR 1	SK 2	REF 1	
ABSY|Ab(2)SM6#16
DT|28 Jan 02
SYN|In(2LR)SM6#16
ID|FBab0024094
REF
{
REFM|FBrf0141259
|Bloomington Drosophila Stock Center
|
|-1
}

DIS|L. Craymer.
MU|X ray
PRG|In(2LR)SM6
CCM|Presumptive additional aberration(s) on @SM6a@ associated with @SM6#16@.
BGV
{
BGVSY|SM6#16
ID|FBba0000102
MK|al<up>2</up> Cy<up>1</up> dp<up>lvI</up> cn<up>2P</up> sp<up>2</up>
IBAL
PRG|SM6a
BSN|SM6#16
PHP|X-ray derivative of @SM6a@, presumably has additional aberrations.
REF|FBrf0141259
SK|FBstBL-1287
|en[Apa]/SM6#16
|FBstBL-1219
|wg[Sp-1] Bl[1] L[rm] Bc[1] Pu[2]/SM6#16
}

SKC|2
}
# EOR
ABSR
{
RETE|ID 1 FBab0024296	CLA 1 Aberration	GSYM 1 Ab(2;?)al<up>ice</up>	DT 1 29 Oct 99	RESZ 325	REF 1	
ABSY|Ab(2;?)al<up>ice</up>
DT|29 Oct 99
ID|FBab0024296
REF
{
REFM|FBrf0064389
|Campbell et al.
|1993
|-1
}

ASAL|FBal0030482 == al<up>ice</up>
MU|ethyl methanesulfonate
CCM|uncharacterized
REFDSR
{
RDID|FBrf0064389
|Campbell et al.
|1993
MU|ethyl methanesulfonate
CCM|uncharacterized
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024297	CLA 1 Aberration	GSYM 1 Ab(2;?)al<up>vin</up>	DT 1 29 Oct 99	RESZ 373	REF 1	
ABSY|Ab(2;?)al<up>vin</up>
DT|29 Oct 99
ID|FBab0024297
REF
{
REFM|FBrf0064389
|Campbell et al.
|1993
|-1
}

ASAL|FBal0030483 == al<up>vin</up>
MU|ethyl methanesulfonate
CCM|uncharacterized; probably an inversion.
REFDSR
{
RDID|FBrf0064389
|Campbell et al.
|1993
MU|ethyl methanesulfonate
CCM|uncharacterized; probably an inversion.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028891	CLA 1 Aberration	GSYM 1 Ab(2;?)dare<up>34</up>	DT 1 12 Nov 00	RESZ 501	REF 1	
ABSY|Ab(2;?)dare<up>34</up>
DT|12 Nov 00
SYN|unnamed
ID|FBab0028891
REF
{
REFM|FBrf0111361
|Freeman et al.
|1999
|-1
}

ASAL|FBal0101458 == dare<up>34</up>
MU|&Dgr;2-3
PRG|dare<up>1</up>
|FBti0009263 == FBti0003650 == P{lacW}dare<up>1</up>
AMD|dare
REFDSR
{
RDID|FBrf0111361
|Freeman et al.
|1999
MU|&Dgr;2-3
PRG|dare<up>1</up>
|FBti0009263 == FBti0003650 == P{lacW}dare<up>1</up>
AMD|dare
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029529	CLA 1 Aberration	GSYM 1 Ab(2;?)wun<up>CE</up>	DT 1 03 Jun 01	RESZ 485	REF 1	
ABSY|Ab(2;?)wun<up>CE</up>
DT|03 Jun 01
SYN|wunen<up>CE</up>
ID|FBab0029529
REF
{
REFM|FBrf0134584
|Starz-Gaiano et al.
|2001
|-1
}

ASAL|FBal0050885 == wun<up>CE</up>
CCM|The @Ab(2;?)wun<up>CE</up>@ lesion has not been characterized.
REFDSR
{
RDID|FBrf0134584
|Starz-Gaiano et al.
|2001
CCM|The @Ab(2;?)wun<up>CE</up>@ lesion has not been characterized.
OTH|@Ab(2;?)wun<up>CE</up>@ affects both @wun@ and @wun2@.
SYN|wunen<up>CE</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023960	CLA 1 Aberration	GSYM 1 Ab(2;3)boss<up>8</up>	DT 1 29 Oct 99	RESZ 387	REF 1	
ABSY|Ab(2;3)boss<up>8</up>
DT|29 Oct 99
SYN|unnamed
ID|FBab0023960
REF
{
REFM|FBrf0051837
|Hart et al.
|1990
|-1
}

ASAL|FBal0019775 == boss<up>8</up>
MU|X ray
CCM|Complex rearrangement.
AMD|boss
REFDSR
{
RDID|FBrf0051837
|Hart et al.
|1990
MU|X ray
CCM|Complex rearrangement.
AMD|boss
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023383	CLA 1 Aberration	NAM 1 eya transvection disruptor	GSYM 1 Ab(2;3)ETD4.4	DT 1 12 Oct 01	RESZ 536	CLOC 1 26D;40;58;81	REF 1	
ABSY|Ab(2;3)ETD4.4
DT|12 Oct 01
NAM|eya transvection disruptor
ID|FBab0023383
REF
{
REFM|FBrf0078888
|Leiserson et al.
|1994
|-1
}

BPT|26D;40;58;81
CCM|All limits from polytene analysis (FBrf0078888)
MU|X ray
PRG|eya<up>4</up>
REFDSR
{
RDID|FBrf0078888
|Leiserson et al.
|1994
BPT|26D;40;58;81
MU|X ray
PRG|eya<up>4</up>
PHP|Disrupts pairing in the eya region, causing suppression of @eya<up>2</up>@/@eya<up>4</up>@
|transvection and a reduction in size of adult eye to less than 3/4.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027547	CLA 1 Aberration	GSYM 1 Ab(2;3)T-1	DT 1 25 Mar 02	RESZ 1387	REF 2	
ABSY|Ab(2;3)T-1
DT|25 Mar 02
SYN|unnamed
|T-1
ID|FBab0027547
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
REFM|FBrf0141552
|Ronsseray et al.
|2001
|-1
}

MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x7@.
|Enhancement is specific for the transgene array at 50C, it does not
|result from mutations in modifiers of PEV (chromosomes with and without
|the transgene array fail to enhance variegation of @w@ in either @In(1)w<up>m4</up>@
|or @P{lacW}92E.x3@).
SYN|unnamed
}

REFDSR
{
RDID|FBrf0141552
|Ronsseray et al.
|2001
OTH|@Ab(2;3)T-1@ significantly represses the occurrence of P-induced dysgenic
|sterility compared to controls in crosses of @Ab(2;3)T-1@ females to
|P males. A stronger repression of P-induced dysgenic sterility is
|seen if the @Ab(2;3)T-1@ females are also carrying @P{lArB}A171.1F1@.
|The array of @P{lacW}@ element on @Ab(2;3)T-1@ can repress germline
|expression of other @P{lacZ}@ insertions, either located on the same
|chromosome at a different site, or on a different chromosome. Repression
|is detected only when the @Ab(2;3)T-1@ chromosome is maternally inherited.
SYN|T-1
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029627	CLA 1 Aberration	GSYM 1 Ab(2;3)Tell	DT 1 22 Aug 04	RESZ 1945	ALESR 2	REF 1	
ABSY|Ab(2;3)Tell
DT|22 Aug 04
SYN|Tell
ID|FBab0029627
REF
{
REFM|FBrf0137374
|Seum et al.
|2000
|-1
}

MU|X ray
COR|Induced on: @P{Winkelried}D@.
REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
MU|X ray
COR|Induced on: @P{Winkelried}D@.
PHP|lethal | recessive
OTH|The @Ab(2;3)Tell@ rearrangement was induced on a chromosome carrying
|@P{Winkelried}D@ and juxtaposes the @P{Winkelried}D@ insertion and
|pericentromeric heterochromatin.
|FlyBase curator comment: the @Ab(2;3)Tell-P{Winkelried}D@ genotype
|variant represents the genotype that carries both the @Ab(2;3)Tell@
|rearrangement and the @P{Winkelried}D@ insertion. The
|@Ab(2;3)Tell-P{Winkelried}D@ variant shows position effect
|variegation for the @w@ gene present in the @P{Winkelried}D@
|insertion.
SYN|Tell
}

BGV
{
BGVSY|Ab(2;3)Tell-P{Winkelried(-FRT)}
ID|FBba0000503
REF|FBrf0137374
REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
TRNA|FBti0018245 == P{Winkelried(-FRT)}D
PRG|Ab(2;3)Tell-P{Winkelried}D
DIS|C. Seum
}

}

BGV
{
BGVSY|Ab(2;3)Tell-P{Winkelried}D
ID|FBba0000504
REF|FBrf0137374
REFDSR
{
RDID|FBrf0137374
|Seum et al.
|2000
MK|Ecol\lacZ<up>Hsp70Bb.-190</up> scs'<up>unspecified</up> scs<up>unspecified</up> w<up>E2F.Scer\UAS</up>
TRNA|FBti0017779 == P{Winkelried}D
OTH|The @Ab(2;3)Tell@ rearrangement was induced on a chromosome carrying
|@P{Winkelried}D@ and juxtaposes the @P{Winkelried}D@ insertion and
|pericentromeric heterochromatin.
|FlyBase curator comment: the @Ab(2;3)Tell-P{Winkelried}D@ genotype
|variant represents the genotype that carries both the @Ab(2;3)Tell@
|rearrangement and the @P{Winkelried}D@ insertion. The
|@Ab(2;3)Tell-P{Winkelried}D@ variant shows position effect
|variegation for the @w@ gene present in the @P{Winkelried}D@
|insertion.
DIS|C. Seum
}

}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024295	CLA 1 Aberration	GSYM 1 Ab(2;3;?)ul10#1	DT 1 12 Nov 00	RESZ 1024	CLOC 1 80;89D;81;22A;40	REF 1	
ABSY|Ab(2;3;?)ul10#1
DT|12 Nov 00
SYN|R(Df(3R)ul10)#1
ID|FBab0024295
REF
{
REFM|FBrf0080101
|Hopmann et al.
|1995
|-1
}

BPT|80;89D;81;22A;40
CCM|All limits from polytene analysis (FBrf0080101)
BIP|89E3;90A2--3 (from Df(3R)ul10)
NCO|Junctions: 1L:2L
|Junctions: 2R:4R
MU|X ray
PRG|Df(3R)ul10
REFDSR
{
RDID|FBrf0080101
|Hopmann et al.
|1995
BPT|80;89D;81;22A;40;het
NCO|Junctions: 1L:2L
|Junctions: 2R:4R
MU|X ray
PRG|Df(3R)ul10
CCM|Cytology described as 61-80/89D-81 + 100-89D/22A-40 + 21-22A/undetermined
|heterochromatin.
PHP|Does not completely block transvection, shows some reduction of alula
|when heterozygous with Cbx alleles of @Ubx@. Causes moderate reduction
|of pigmentation in posterior segments when heterozygous with @Df(3R)Ubx-RS4-8@.
|Causes strong disruption of pairing at BX-C in salivary chromosomes
|when heterozygous with wild type.
OTH|Selected on basis of ability to suppress transvection in @Ubx@<up>Cbx</up>
|heterozygotes.
SYN|R(Df(3R)ul10)#1
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023384	CLA 1 Aberration	GSYM 1 Ab(2L;?)34Cy<up>rv</up>	DT 1 12 Nov 00	RESZ 418	CLOC 1 23B1--2	REF 1	
ABSY|Ab(2L;?)34Cy<up>rv</up>
DT|12 Nov 00
SYN|unnamed
ID|FBab0023384
REF
{
REFM|FBrf0076536
|Littleton and Bellen
|1994
|-1
}

BPT|23B1--2
CCM|All limits from polytene analysis (FBrf0076536)
MU|&ggr; ray
REFDSR
{
RDID|FBrf0076536
|Littleton and Bellen
|1994
BPT|23B1--2
MU|&ggr; ray
CCM|Complex rearrangement.
PHP|Reversion of the dominant curly wing phenotype.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023372	CLA 1 Aberration	GSYM 1 Ab(2L;?)eya<up>X11</up>	DT 1 12 Oct 01	RESZ 336	REF 1	
ABSY|Ab(2L;?)eya<up>X11</up>
DT|12 Oct 01
SYN|Ab(2L;?)cli<up>eya-X11</up>
ID|FBab0023372
REF
{
REFM|FBrf0057885
|Bonini et al.
|1993
|-1
}

ASAL|FBal0030783 == eya<up>X11</up>
MU|X ray
REFDSR
{
RDID|FBrf0057885
|Bonini et al.
|1993
MU|X ray
OTH|Has complex cytology: not all breakpoints determined.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023373	CLA 1 Aberration	GSYM 1 Ab(2L;?)eya<up>X9</up>	DT 1 12 Oct 01	RESZ 333	REF 1	
ABSY|Ab(2L;?)eya<up>X9</up>
DT|12 Oct 01
SYN|Ab(2L;?)cli<up>eya-X9</up>
ID|FBab0023373
REF
{
REFM|FBrf0057885
|Bonini et al.
|1993
|-1
}

ASAL|FBal0030789 == eya<up>X9</up>
MU|X ray
REFDSR
{
RDID|FBrf0057885
|Bonini et al.
|1993
MU|X ray
OTH|Has complex cytology: not all breakpoints determined.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023385	CLA 1 Aberration	GSYM 1 Ab(2L;?)her<up>3</up>	DT 1 29 Oct 99	RESZ 317	CLOC 1 36A	REF 1	
ABSY|Ab(2L;?)her<up>3</up>
DT|29 Oct 99
ID|FBab0023385
REF
{
REFM|FBrf0068639
|Pultz et al.
|1994
|-1
}

ASAL|FBal0039401 == her<up>3</up>
BPT|36A
CCM|All limits from polytene analysis (FBrf0068639)
MU|X ray
REFDSR
{
RDID|FBrf0068639
|Pultz et al.
|1994
BPT|36A
MU|X ray
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027548	CLA 1 Aberration	GSYM 1 Ab(2LR)C-2	DT 1 25 Mar 02	RESZ 1824	CLOC 1 h35--h46;42A;51F	ALESR 1	REF 3	
ABSY|Ab(2LR)C-2
DT|25 Mar 02
SYN|unnamed
|C-2
ID|FBab0027548
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
REFM|FBrf0141552
|Ronsseray et al.
|2001
|-1
REFM|FBrf0105816
|Fanti et al.
|1998
|-1
}

BPT|h35--h46;42A;51F
CCM|All limits from polytene analysis (FBrf0099191)
MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
BPT|h35--h46;42A;51F
MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
PHP|Homozygous viable.
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x7@.
|Enhancement is specific for the transgene array at 50C, it does not
|result from mutations in modifiers of PEV (chromosomes with and without
|the transgene array fail to enhance variegation of @w@ in either @In(1)w<up>m4</up>@
|or @P{lacW}92E.x3@).
SYN|unnamed
}

REFDSR
{
RDID|FBrf0141552
|Ronsseray et al.
|2001
OTH|Does not show significant repression of P-induced dysgenic sterility
|when @Ab(2LR)C-2@ females are crossed to P males. Does show significant
|repression of P-induced dysgenic sterility when females carrying both
|@P{lArB}A171.1F1@ and @Ab(2LR)C-2@ are crossed to P males.
SYN|C-2
}

BGV
{
BGVSY|Ab(2LR)C-2-w
SYN|unnamed
ID|FBba0000230
REF|FBrf0099191
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
SYN|unnamed
PHP|@P{lacW}50C.x7@ array is lost by recombination or transposase activity.
|Enhancement of @P{lacW}50C.x7@ variegation also occurs when in trans
|to the rearrangement, this suggests transvection is not the cause of
|the enhancement. Increased proximity of the array to heterochromatin
|in either cis or trans can increase the strength of transgene silencing.
}

}

}
# EOR
ABSR
{
RETE|ID 1 FBab0037786	CLA 1 Aberration	GSYM 1 Ab(2R)55-20	DT 1 22 Aug 04	RESZ 2599	REF 1	
ABSY|Ab(2R)55-20
DT|22 Aug 04
SYN|55-20
ID|FBab0037786
REF
{
REFM|FBrf0145131
|Goldstein et al.
|2001
|-1
}

MU|diepoxybutane
AMD|TER94
|l(2)46Ci
|l(2)46CFn
AMDD|Mef2
|l(2)46CDa
|eve
|Adam
|l(2)46Dj
|l(2)46Dh
|l(2)46Di
|l(2)46Ck
|l(2)46Cn
|Jra
|14-3-3&zgr;
|l(2)46Eb
|l(2)46Ed
|l(2)46Fb
|l(2)46Cm
|l(2)46Ei
|l(2)46Cl
|l(2)46Ej
|l(2)46Cj
|l(2)46Ea
|l(2)46Fa
|l(2)46Eg
|l(2)46Eh
|l(2)46Ec
|Hr46
|Syb
REFDSR
{
RDID|FBrf0145131
|Goldstein et al.
|2001
MU|diepoxybutane
AMD|TER94
|l(2)46Ci
|l(2)46CFn
AMDD|Mef2
|l(2)46CDa
|eve
|Adam
|l(2)46Dj
|l(2)46Dh
|l(2)46Di
|l(2)46Ck
|l(2)46Cn
|Jra
|14-3-3&zgr;
|l(2)46Eb
|l(2)46Ed
|l(2)46Fb
|l(2)46Cm
|l(2)46Ei
|l(2)46Cl
|l(2)46Ej
|l(2)46Cj
|l(2)46Ea
|l(2)46Fa
|l(2)46Eg
|l(2)46Eh
|l(2)46Ec
|Hr46
|Syb
OTH|The "55-20" line has a very complex pattern of failing to complement
|other mutations, and can be postulated to carry multiple small deletions.
SYN|55-20
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0037787	CLA 1 Aberration	GSYM 1 Ab(2R)89-22	DT 1 22 Aug 04	RESZ 2563	REF 1	
ABSY|Ab(2R)89-22
DT|22 Aug 04
SYN|89-22
ID|FBab0037787
REF
{
REFM|FBrf0145131
|Goldstein et al.
|2001
|-1
}

MU|&ggr; ray
AMD|Mef2
|l(2)46CDa
|eve
|Adam
|TER94
AMDD|l(2)46Ci
|l(2)46CFn
|l(2)46Dj
|l(2)46Dh
|l(2)46Di
|l(2)46Ck
|l(2)46Cn
|Jra
|14-3-3&zgr;
|l(2)46Eb
|l(2)46Ed
|l(2)46Fb
|l(2)46Cm
|l(2)46Ei
|l(2)46Cl
|l(2)46Ej
|l(2)46Cj
|l(2)46Ea
|l(2)46Fa
|l(2)46Eg
|l(2)46Eh
|l(2)46Ec
|Hr46
|Syb
REFDSR
{
RDID|FBrf0145131
|Goldstein et al.
|2001
MU|&ggr; ray
AMD|Mef2
|l(2)46CDa
|eve
|Adam
|TER94
AMDD|l(2)46Ci
|l(2)46CFn
|l(2)46Dj
|l(2)46Dh
|l(2)46Di
|l(2)46Ck
|l(2)46Cn
|Jra
|14-3-3&zgr;
|l(2)46Eb
|l(2)46Ed
|l(2)46Fb
|l(2)46Cm
|l(2)46Ei
|l(2)46Cl
|l(2)46Ej
|l(2)46Cj
|l(2)46Ea
|l(2)46Fa
|l(2)46Eg
|l(2)46Eh
|l(2)46Ec
|Hr46
|Syb
OTH|The "89-22" line has a very complex pattern of failing to complement
|other mutations, and can be postulated to carry multiple small deletions.
SYN|89-22
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028057	CLA 1 Aberration	GSYM 1 Ab(2R)ClassII	DT 1 29 Oct 99	RESZ 767	REF 1	
ABSY|Ab(2R)ClassII
DT|29 Oct 99
ID|FBab0028057
REF
{
REFM|FBrf0102481
|Salinas et al.
|1998
|-1
}

ASAL|FBal0089833 == Asx<up>II</up>
|FBal0089370 == cpsf<up>II</up>
MU|&Dgr;2-3
PRG|Asx<up>P1</up>
CCM|Complex rearrangement.
AMD|Asx
|cpsf
REFDSR
{
RDID|FBrf0102481
|Salinas et al.
|1998
MU|&Dgr;2-3
PRG|Asx<up>P1</up>
CCM|Complex rearrangement.
AMD|Asx
|cpsf
PHP|Most embryos show head defects and may exhibit weak posterior transformations
|of the sixth and seventh abdominal segment towards the eighth. Most
|embryos also show reduction of the H-piece and deposits of yellow,
|chitinous material in the cuticle.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028058	CLA 1 Aberration	GSYM 1 Ab(2R)ClassV	DT 1 29 Oct 99	RESZ 492	REF 1	
ABSY|Ab(2R)ClassV
DT|29 Oct 99
ID|FBab0028058
REF
{
REFM|FBrf0102481
|Salinas et al.
|1998
|-1
}

ASAL|FBal0089367 == cpsf<up>V</up>
MU|&Dgr;2-3
PRG|Asx<up>P1</up>
CCM|Breakpoints and nature of the rearrangement are not mapped.
AMD|cpsf
REFDSR
{
RDID|FBrf0102481
|Salinas et al.
|1998
MU|&Dgr;2-3
PRG|Asx<up>P1</up>
CCM|Breakpoints and nature of the rearrangement are not mapped.
AMD|cpsf
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024809	CLA 1 Aberration	GSYM 1 Ab(2R)dpn<up>8</up>	DT 1 29 Oct 99	RESZ 432	CLOC 1 44C	REF 1	
ABSY|Ab(2R)dpn<up>8</up>
DT|29 Oct 99
ID|FBab0024809
REF
{
REFM|FBrf0084726
|Barbash and Cline
|1995
|-1
}

ASAL|FBal0049434 == dpn<up>8</up>
BPT|44C
CCM|All limits from polytene analysis (FBrf0084726)
MU|spontaneous
AMD|dpn
REFDSR
{
RDID|FBrf0084726
|Barbash and Cline
|1995
BPT|44C
MU|spontaneous
CCM|Small alteration in proximal 44C.
AMD|dpn
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027354	CLA 1 Deficiency (cytologically invisible)	GSYM 1 Ab(2R)IR36	DT 1 09 Mar 99	RESZ 832	CLOC 1 [<h35];[>h35]	REF 1	
ABSY|Ab(2R)IR36
DT|09 Mar 99
SYN|l(2Rh)IR36
ID|FBab0027354
REF
{
REFM|FBrf0094580
|Dimitri et al.
|1997
|-1
}

BPT|[<h35];[>h35]
CCM|Right limit of break 1 from complementation mapping against l(2)40Ff (FBrf0094580)
|Left limit of break 2 from complementation mapping against l(2)40Fe (FBrf0094580)
ACLA|Deficiency (cytologically invisible)
MU|IR-hybrid dysgenesis
AMD|l(2)40Fe
|l(2)40Ff
|l(2)40Fg
|lt
REFDSR
{
RDID|FBrf0094580
|Dimitri et al.
|1997
BPT|[];[]
ACLA|Deficiency (cytologically invisible)
MU|IR-hybrid dysgenesis
AMD|l(2)40Fe
|l(2)40Ff
|l(2)40Fg
|lt
SYN|l(2Rh)IR36
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027355	CLA 1 Deficiency (cytologically invisible)	GSYM 1 Ab(2R)IR45	DT 1 06 Jan 99	RESZ 487	CLOC 1 [];[]	REF 1	
ABSY|Ab(2R)IR45
DT|06 Jan 99
SYN|l(2Rh)IR45
ID|FBab0027355
REF
{
REFM|FBrf0094580
|Dimitri et al.
|1997
|-1
}

BPT|[];[]
ACLA|Deficiency (cytologically invisible)
MU|IR-hybrid dysgenesis
AMDD|l(2)40Fc
REFDSR
{
RDID|FBrf0094580
|Dimitri et al.
|1997
BPT|[];[]
ACLA|Deficiency (cytologically invisible)
MU|IR-hybrid dysgenesis
AMDD|l(2)40Fc
SYN|l(2Rh)IR45
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027947	CLA 1 Aberration	GSYM 1 Ab(3)BTD4	DT 1 16 Nov 01	RESZ 388	REF 1	
ABSY|Ab(3)BTD4
DT|16 Nov 01
SYN|Bithorax Transvection Disrupter rearrangement 4
ID|FBab0027947
REF
{
REFM|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
|-1
}

MU|&ggr; ray
CCM|Normal.
REFDSR
{
RDID|FBrf0046365
|Smolik-Utlaut and Gelbart
|1987
MU|&ggr; ray
CCM|Normal.
PHP|@z@ disrupted phenotype.
SYN|Bithorax Transvection Disrupter rearrangement 4
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027356	CLA 1 Aberration	GSYM 1 Ab(3)JY16	DT 1 29 Oct 99	RESZ 551	REF 2	
ABSY|Ab(3)JY16
DT|29 Oct 99
ID|FBab0027356
REF
{
REFM|FBrf0054607
|Breen and Harte
|1991
|-1
REFM|FBrf0108148
|Breen
|1999
|-1
}

ASAL|FBal0096650 == trx<up>JY16</up>
AMD|trx
REFDSR
{
RDID|FBrf0054607
|Breen and Harte
|1991
CCM|Chromosomal rearrangement is unknown.
|Chromosome fails to complement @trx@ and mutations of flanking loci.
AMD|trx
}

REFDSR
{
RDID|FBrf0108148
|Breen
|1999
CCM|Rearrangement may be a small inversion.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0025193	CLA 1 Aberration	GSYM 1 Ab(3;?)comm<up>4</up>	DT 1 12 Nov 00	RESZ 490	CLOC 1 70C1--2;71E3--5	REF 1	
ABSY|Ab(3;?)comm<up>4</up>
DT|12 Nov 00
ID|FBab0025193
REF
{
REFM|FBrf0089842
|Tear et al.
|1996
|-1
}

ASAL|FBal0051697 == comm<up>4</up>
BPT|70C1--2;71E3--5
CCM|All limits from polytene analysis (FBrf0089842)
MU|X ray
AMD|comm
REFDSR
{
RDID|FBrf0089842
|Tear et al.
|1996
BPT|70C1--2;71E3--5;het
MU|X ray
CCM|Rearrangement breakpoint at 71E3--71E5 lies 40kb distal to the @comm@
|transcription unit.
AMD|comm
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024298	CLA 1 Aberration	GSYM 1 Ab(3;?)Csr-rv7	DT 1 12 Nov 00	RESZ 507	CLOC 1 93F2--4;h47--h58	REF 1	
ABSY|Ab(3;?)Csr-rv7
DT|12 Nov 00
ID|FBab0024298
REF
{
REFM|FBrf0084260
|Pereira et al.
|1995
|-1
}

BPT|93F2--4;h47--h58
CCM|All limits from polytene analysis (FBrf0084260)
MU|&ggr; ray
PRG|Csr<up>3</up>
REFDSR
{
RDID|FBrf0084260
|Pereira et al.
|1995
BPT|93F2--4;h47--h58
MU|&ggr; ray
PRG|Csr<up>3</up>
CCM|Either a paracentric inversion of a T(3;4).
PHP|Chromosome is temperature-sensitive recessive lethal.
OTH|Induced on chromosome carrying @Csr<up>rv7</up>@.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024299	CLA 1 Aberration	GSYM 1 Ab(3;?)D24,D18#6	DT 1 12 Nov 00	RESZ 933	CLOC 1 80--81;62F	REF 1	
ABSY|Ab(3;?)D24,D18#6
DT|12 Nov 00
SYN|R(abd-A<up>D24</up>Abd-B<up>D18</up>)#6
ID|FBab0024299
REF
{
REFM|FBrf0080101
|Hopmann et al.
|1995
|-1
}

BPT|80--81;62F
CCM|All limits from polytene analysis (FBrf0080101)
MU|X ray
PRG|abd-A<up>D24</up>
|Abd-B<up>D18</up>
REFDSR
{
RDID|FBrf0080101
|Hopmann et al.
|1995
BPT|80--81;62F
MU|X ray
PRG|abd-A<up>D24</up>
|Abd-B<up>D18</up>
CCM|New order stated as: 100-81/62F-61A/unknown short segment/62F/80.
PHP|Causes moderate pairing disruption of BX-C in salivary gland nuclei.
|A5 and A6 identities are indistinguishable from those seen in unrearranged
|@Dp(3;2)D109@; @abd-A<up>D24</up>@,@Abd-B<up>D18</up>@/@Df(3R)Ubx-RS4-8@ adults,
|and this phenotype is not affected by @T(2;3)bw<up>VDe3</up>@.
OTH|Selected on basis of ability to suppress transvection in @Ubx@<up>Cbx</up>
|heterozygotes.
SYN|R(abd-A<up>D24</up>Abd-B<up>D18</up>)#6
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024300	CLA 1 Aberration	GSYM 1 Ab(3;?)D24,D18#8	DT 1 27 Aug 98	RESZ 903	CLOC 1 86F	REF 1	
ABSY|Ab(3;?)D24,D18#8
DT|27 Aug 98
SYN|R(abd-A<up>D24</up>Abd-B<up>D18</up>)#8
ID|FBab0024300
REF
{
REFM|FBrf0080101
|Hopmann et al.
|1995
|-1
}

BPT|86F
CCM|All limits from polytene analysis (FBrf0080101)
MU|X ray
PRG|abd-A<up>D24</up>
|Abd-B<up>D18</up>
REFDSR
{
RDID|FBrf0080101
|Hopmann et al.
|1995
BPT|86F;het
MU|X ray
PRG|abd-A<up>D24</up>
|Abd-B<up>D18</up>
CCM|Second break in undetermined heterochromatin.
PHP|Causes moderate pairing disruption of BX-C in salivary gland nuclei.
|A5 and A6 identities are indistinguishable from those seen in unrearranged
|@Dp(3;2)D109@; @abd-A<up>D24</up>@,@Abd-B<up>D18</up>@/@Df(3R)Ubx-RS4-8@ adults,
|and this phenotype is not affected by @T(2;3)bw<up>VDe3</up>@.
OTH|Selected on basis of ability to suppress transvection in @Ubx@<up>Cbx</up>
|heterozygotes.
SYN|R(abd-A<up>D24</up>Abd-B<up>D18</up>)#8
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0014439	CLA 1 Aberration	GSYM 1 Ab(3;?)ss<up>D114.7</up>	DT 1 29 Oct 99	RESZ 388	CLOC 1 89C	REF 1	
ABSY|Ab(3;?)ss<up>D114.7</up>
DT|29 Oct 99
ID|FBab0014439
REF
{
REFM|FBrf0102306
|Duncan et al.
|1998
|-1
}

ASAL|FBal0090120 == ss<up>D114.7</up>
BPT|89C
CCM|All limits from polytene analysis (FBrf0102306)
MU|X ray
AMD|ss
REFDSR
{
RDID|FBrf0102306
|Duncan et al.
|1998
BPT|89C;het
MU|X ray
AMD|ss
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023377	CLA 1 Aberration	GSYM 1 Ab(3L;?)Rdl<up>20</up>	DT 1 29 Oct 99	RESZ 613	CLOC 1 66F	REF 2	
ABSY|Ab(3L;?)Rdl<up>20</up>
DT|29 Oct 99
SYN|InvRdl-20
ID|FBab0023377
REF
{
REFM|FBrf0055003
|ffrench-Constant et al.
|1991
|-1
REFM|FBrf0058168
|ffrench-Constant
|1993
|-1
}

ASAL|FBal0030107 == Rdl<up>20</up>
BPT|66F
CCM|All limits from polytene analysis (FBrf0055003)
MU|&ggr; ray
REFDSR
{
RDID|FBrf0055003
|ffrench-Constant et al.
|1991
BPT|66F
MU|&ggr; ray
CCM|Complex rearrangement with one break in the 66F region and three others.
}

REFDSR
{
RDID|FBrf0058168
|ffrench-Constant
|1993
SYN|InvRdl-20
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0024810	CLA 1 Aberration	GSYM 1 Ab(3L;h)GI1a	DT 1 31 Aug 01	RESZ 791	REF 2	
ABSY|Ab(3L;h)GI1a
DT|31 Aug 01
SYN|fz<up>GI1a</up>
|GI1a
|Ab(3L;h?)GI1a
ID|FBab0024810
REF
{
REFM|FBrf0064754
|Wong and Adler
|1993
|-1
REFM|FBrf0051945
|Adler et al.
|1990
|-1
}

MU|&ggr; ray
CCM|Chromosomal rearrangement with the @fz@ locus juxtaposed to centromeric
|heterochromatin.
PED|position-effect variegation for: fz
REFDSR
{
RDID|FBrf0051945
|Adler et al.
|1990
MU|&ggr; ray
CCM|Chromosomal rearrangement with the @fz@ locus juxtaposed to centromeric
|heterochromatin.
PED|position-effect variegation for: fz
PHP|This rearrangement has a weak @fz@ phenotype, probably due to position
|effect variegation.
SYN|fz<up>GI1a</up>
}

REFDSR
{
RDID|FBrf0064754
|Wong and Adler
|1993
SYN|GI1a
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023374	CLA 1 Aberration	GSYM 1 Ab(3L;h)ME178	DT 1 31 Aug 01	RESZ 1855	CLOC 1 78A7--B1	SK 1	REF 3	
ABSY|Ab(3L;h)ME178
DT|31 Aug 01
SYN|Ab(3L;h?)ME178
ID|FBab0023374
REF
{
REFM|FBrf0089804
|Russell et al.
|1996
|-1
REFM|FBrf0106081
|Carpenter
|1998.11.24
|-1
REFM|FBrf0075380
|Carpenter
|1994
|-1
}

ASAL|FBal0094488 == l(3)78Ad<up>1</up>
BPT|78A7--B1
CCM|All limits from polytene analysis (FBrf0075380)
DIS|A.T.C. Carpenter.
MU|X ray
OAB|Fails to complement 78C deficiencies (no visible cytological defect)
|and fails to complement 78A deficiencies.
REFDSR
{
RDID|FBrf0075380
|Carpenter
|1994
BPT|78A7--B1;het
DIS|A.T.C. Carpenter.
MU|X ray
CCM|May be a translocation or an inversion.
AMDD|l(3)78Aa
|l(3)78Ab
|l(3)78Ac
OTH|Lethal in 78A and 78C, although there is no visible cytological defect
|there even in asynapsed chromosomes. Mapping of the lethal is complicated
|by the facts that when @Ab(3L;h)ME178@ is transmitted by the mother
|it is viable over most other 78C lethals and deficiencies, and even
|when it is transmitted by the father it leaks. It is nearly lethal
|over most @Pc@ deficiencies, including @In(3)Pc-T7@ and @Pc<up>3</up>@ and
|@Ubx@ duplication, but is less lethal over @Df(3L)Pc-30A@ is viable
|over @Pc<up>73</up>@ and @Df(3L)ME1325@. Lethal over @In(3)80c@ even when
|transmitted from female. Completely lethal over @Df(3L)ME107@ from
|78A lesion so 78C lesion cannot be tested. Not phenotypically @Pc@.
}

REFDSR
{
RDID|FBrf0089804
|Russell et al.
|1996
BPT|78A7--B1;het
MU|X ray
CCM|Maybe an inversion or translocation.
OAB|Fails to complement 78C deficiencies (no visible cytological defect)
|and fails to complement 78A deficiencies.
}

REFDSR
{
RDID|FBrf0106081
|Carpenter
|1998.11.24
AMD|l(3)78Ad
}

SK|FBstBL-4904
|Ab(3L;h)ME178, mwh[1] l(3)78Ad[1] red[1] e[4]/TM2
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0023375	CLA 1 Aberration	GSYM 1 Ab(3L;h)ME200	DT 1 31 Aug 01	RESZ 1117	CLOC 1 78D1--3	REF 2	
ABSY|Ab(3L;h)ME200
DT|31 Aug 01
SYN|Ab(3L;h?)ME200
ID|FBab0023375
REF
{
REFM|FBrf0089804
|Russell et al.
|1996
|-1
REFM|FBrf0075380
|Carpenter
|1994
|-1
}

BPT|78D1--3
CCM|All limits from polytene analysis (FBrf0075380)
DIS|A.T.C. Carpenter.
MU|X ray
REFDSR
{
RDID|FBrf0075380
|Carpenter
|1994
BPT|78D1--3;het
DIS|A.T.C. Carpenter.
MU|X ray
CCM|May be a translocation or an inversion.
OTH|Position-effect lethal; viability over
|deficiencies increases in the presence of an extra Y. Mapping of the
|lethal is
|complicated by the facts that when @Ab(3L;h)ME200@ is transmitted by
|the mother it is viable over everything, and even when it is transmitted
|by the father it leaks. Without an extra Y it is nearly lethal over
|most @Pc@ deficiencies but less lethal over @Df(3L)Pc-30A@, @Pc<up>3</up>@
|and @Ubx@ duplication, @Pc<up>73</up>@, @Df(3L)Pc-MK@, @Df(3L)ME107@ and @In(3)Pc-T7@
|viable over @In(3)80c@. Not phenotypically @Pc@.
}

REFDSR
{
RDID|FBrf0089804
|Russell et al.
|1996
BPT|78D1--3;het
MU|X ray
CCM|Maybe an inversion or translocation.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023376	CLA 1 Aberration	GSYM 1 Ab(3L;h)Pc-109	DT 1 31 Aug 01	RESZ 1346	CLOC 1 78C3--9	REF 2	
ABSY|Ab(3L;h)Pc-109
DT|31 Aug 01
SYN|Ab(3L;h?)Pc-109
ID|FBab0023376
REF
{
REFM|FBrf0089804
|Russell et al.
|1996
|-1
REFM|FBrf0075380
|Carpenter
|1994
|-1
}

BPT|78C3--9
CCM|All limits from polytene analysis (FBrf0075380)
DIS|A.T.C. Carpenter.
MU|X ray
OAB|Even with an extra Y, remains lethal over @Df(3L)Pc-101@.
PED|position-effect variegation for: Pc
|position-effect variegation for: ppl
REFDSR
{
RDID|FBrf0075380
|Carpenter
|1994
BPT|78C3--9;het
DIS|A.T.C. Carpenter.
MU|X ray
CCM|May be a translocation or an inversion.
AMDD|l(3)78Da
PED|position-effect variegation for: Pc
|position-effect variegation for: ppl
OTH|Position-effect
|variegating lethal for @Pc@, @ppl@ and the lethality of @In(3)80c@
|since rescuable by addition of a Y chromosome; however, even with
|an extra Y, remains lethal over @Df(3L)Pc-101@.
}

REFDSR
{
RDID|FBrf0089804
|Russell et al.
|1996
BPT|78C3--9;het
MU|X ray
CCM|Maybe an inversion or a translocation.
AMD|ppl
|Pc
AMDD|Ilk
|l(3)78Da
OAB|Even with an extra Y, remains lethal over @Df(3L)Pc-101@.
PHP|Position-effect variegating lethal for @Pc@, @ppl@ and the lethality
|of @In(3)80c@ since rescuable by addition of a Y chromosome.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023378	CLA 1 Aberration	GSYM 1 Ab(3R;?)A4-4L4	DT 1 28 Jan 02	RESZ 668	REF 2	
ABSY|Ab(3R;?)A4-4L4
DT|28 Jan 02
SYN|R(3R)A4-4L4
|l(3)A4-4L4
ID|FBab0023378
REF
{
REFM|FBrf0056442
|Pereira et al.
|1992
|-1
REFM|FBrf0055967
|Garzino et al.
|1992
|-1
}

ASAL|FBal0032163 == mod<up>L4</up>
MU|&Dgr;2-3
PRG|FBti0001478 == FBti0001300 == P{wA}4-4
AMD|mod
OAB|Lethal in combination with @Df(3R)AP4@.
REFDSR
{
RDID|FBrf0055967
|Garzino et al.
|1992
AMD|mod
SYN|R(3R)A4-4L4
}

REFDSR
{
RDID|FBrf0056442
|Pereira et al.
|1992
MU|&Dgr;2-3
PRG|FBti0001478 == FBti0001300 == P{wA}4-4
OAB|Lethal in combination with @Df(3R)AP4@.
SYN|l(3)A4-4L4
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023379	CLA 1 Aberration	GSYM 1 Ab(3R;?)faf<up>BX13</up>	DT 1 29 Oct 99	RESZ 339	REF 1	
ABSY|Ab(3R;?)faf<up>BX13</up>
DT|29 Oct 99
ID|FBab0023379
REF
{
REFM|FBrf0055917
|Fischer-Vize et al.
|1992
|-1
}

ASAL|FBal0031247 == faf<up>BX13</up>
MU|X ray
REFDSR
{
RDID|FBrf0055917
|Fischer-Vize et al.
|1992
MU|X ray
OTH|Complicated rearrangement involving the tip of chromosome 3R.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023380	CLA 1 Aberration	GSYM 1 Ab(3R;?)faf<up>BX9</up>	DT 1 29 Oct 99	RESZ 337	REF 1	
ABSY|Ab(3R;?)faf<up>BX9</up>
DT|29 Oct 99
ID|FBab0023380
REF
{
REFM|FBrf0055917
|Fischer-Vize et al.
|1992
|-1
}

ASAL|FBal0031256 == faf<up>BX9</up>
MU|X ray
REFDSR
{
RDID|FBrf0055917
|Fischer-Vize et al.
|1992
MU|X ray
OTH|Complicated rearrangement involving the tip of chromosome 3R.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0023381	CLA 1 Aberration	GSYM 1 Ab(3R;h)82Fj<up>1</up>	DT 1 31 Aug 01	RESZ 658	CLOC 1 [];83A1--2	SK 1	REF 2	
ABSY|Ab(3R;h)82Fj<up>1</up>
DT|31 Aug 01
SYN|Ab(het;3R)82Fj<up>1</up>
|Ab(3R;?)82Fj<up>1</up>
|Ab(3R;h?)82Fj<up>1</up>
|Ab(3R;het)82Fj<up>1</up>
ID|FBab0023381
REF
{
REFM|FBrf0075380
|Carpenter
|1994
|-1
REFM|FBrf0111824
|Carpenter
|1999
|-1
}

ASAL|FBal0031906 == l(3)82Fj<up>1</up>
BPT|[];83A1--2
CCM|All limits from polytene analysis (FBrf0075380)
DIS|A.T.C. Carpenter.
MU|X ray
REFDSR
{
RDID|FBrf0075380
|Carpenter
|1994
BPT|het;83A1+
DIS|A.T.C. Carpenter.
MU|X ray
CCM|May be a translocation or an inversion.
}

REFDSR
{
RDID|FBrf0111824
|Carpenter
|1999
BPT|het;83A1+
MU|X ray
SYN|Ab(het;3R)82Fj<up>1</up>
}

SK|FBstBL-4905
|Ab(3R;h)82Fj[1], mwh[1] l(3)82Fj[1] red[1] e[4]/TM3, Sb[1] Ser[1]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010379	CLA 1 Translocation	GSYM 1 Ab(3R;h)Cha<up>l3</up>	DT 1 31 Aug 01	RESZ 502	CLOC 1 [];91C7	REF 1	
ABSY|Ab(3R;h)Cha<up>l3</up>
DT|31 Aug 01
SYN|Ab(3R;h?)Cha<up>l3</up>
ID|FBab0010379
REF
{
REFM|745375211
|Myers and W.M. Gelbart
|Cited in Lindsley and Zimm
|-1
|1992
}

ASAL|FBal0001605 == Cha<up>l3</up>
BPT|[];91C7
ACLA|Translocation
DIS|Myers and Gelbart.
MU|X ray
CCM|Left limit of break 2 from complementation mapping against Cha (citation unavailable)
|Right limit of break 2 from polytene analysis (citation unavailable)
FGD|bk2 hits Cha
REFDSR
{
RDID|745375211
|Myers and W.M. Gelbart
|Cited in Lindsley and Zimm
BPT|het;91C
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027948	CLA 1 Aberration	GSYM 1 Ab(4)ci<up>+</up>1	DT 1 16 Jun 98	RESZ 227	REF 1	
ABSY|Ab(4)ci<up>+</up>1
DT|16 Jun 98
SYN|R<up>1</up>(+)
ID|FBab0027948
REF
{
REFM|FBrf0006600
|Stern et al.
|1946
|-1
}

REFDSR
{
RDID|FBrf0006600
|Stern et al.
|1946
SYN|R<up>1</up>(+)
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027949	CLA 1 Aberration	GSYM 1 Ab(4)ci<up>+</up>7	DT 1 16 Jun 98	RESZ 213	REF 1	
ABSY|Ab(4)ci<up>+</up>7
DT|16 Jun 98
SYN|R(7)(+)
ID|FBab0027949
REF
{
REFM|FBrf0006600
|Stern et al.
|1946
|-1
}

REFDSR
{
RDID|FBrf0006600
|Stern et al.
|1946
SYN|R(7)(+)
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029421	CLA 1 Aberration	GSYM 1 Ab(Y)Y146	DT 1 21 Dec 00	RESZ 4336	CLOC 1 h21;h4	REF 1	
ABSY|Ab(Y)Y146
DT|21 Dec 00
SYN|Y146
ID|FBab0029421
REF
{
REFM|FBrf0127362
|Timakov and Zhang
|2000
|-1
}

BPT|h21;h4
MU|&ggr; ray
PRG|Dp(1;Y)B<up>S</up>Yy<up>+</up>
CCM|New order: h1-h21 | h4-h1 (a duplication of h1-h4 and a deletion of
|h22-h25).
MK|B<up>S</up>
OAB|X/@Ab(Y)Y146@/@Dp(1;Y)y<up>+</up>@ males are sterile. Testes show a departure
|from normal development at early postmeiotic stages of spermatid differentiation.
|Before nuclear elongation, round spermatid nuclei begin to fall apart
|in a large number of spermatid bundles, resulting in singular nuclei
|heads that are dispersed throughout the tails. In approximately 10%
|of males, the testes contain exclusively round spermatids scattered
|throughout the length of the tails. Many of the spermatid bundles
|with scattered nuclei are much smaller in diameter than normal, suggesting
|that some of the spermatid tails fail to develop. However, some spermatid
|bundles show aligned nuclear heads associated with individualization
|complexes, as in wild type.
|@C(1;YS)1@/@Ab(Y)Y146@ males are fertile.
|@Ab(Y)Y146@ is not complemented by @Ts(1Rt;YSt)V8@.
|@Ab(Y)Y146@ is complemented by @Ts(1Rt;YSt)W19@.
|@Ts(1Lt;YSt)P7@/@Ab(Y)Y146@ males produce large numbers of progeny,
|comparable to wild-type X/Y males.
|@Ts(1Lt;YSt)W27@/@Ab(Y)Y146@ males produce large numbers of progeny,
|comparable to wild-type X/Y males.
|@Ts(1Lt;YSt)V24@/@Ab(Y)Y146@ males show a significant reduction in
|male fertility compared to wild type; 19% of males fail to produce
|any progeny, 46% produce very small numbers of progeny (less than 40/male)
|and only 10% produce more than 80 progeny/male. Postmeiotic defects
|are seen in the testes; spermatid bundles with scattered singular nuclear
|heads are seen frequently, but account only for a small proportion
|of spermatid bundles. Some individualization complexes are located
|away from the nuclear bundles, apparently resulting from caudal movement
|along the tails (as occurs in wild type). Individualised spermatids
|are seen in the basal region of the testes and mature sperm are seen
|in the seminal vesicles.
REFDSR
{
RDID|FBrf0127362
|Timakov and Zhang
|2000
BPT|h21;h4
MU|&ggr; ray
PRG|Dp(1;Y)B<up>S</up>Yy<up>+</up>
CCM|New order: h1-h21 | h4-h1 (a duplication of h1-h4 and a deletion of
|h22-h25).
MK|B<up>S</up>
OAB|X/@Ab(Y)Y146@/@Dp(1;Y)y<up>+</up>@ males are sterile. Testes show a departure
|from normal development at early postmeiotic stages of spermatid differentiation.
|Before nuclear elongation, round spermatid nuclei begin to fall apart
|in a large number of spermatid bundles, resulting in singular nuclei
|heads that are dispersed throughout the tails. In approximately 10%
|of males, the testes contain exclusively round spermatids scattered
|throughout the length of the tails. Many of the spermatid bundles
|with scattered nuclei are much smaller in diameter than normal, suggesting
|that some of the spermatid tails fail to develop. However, some spermatid
|bundles show aligned nuclear heads associated with individualization
|complexes, as in wild type.
|@C(1;YS)1@/@Ab(Y)Y146@ males are fertile.
|@Ab(Y)Y146@ is not complemented by @Ts(1Rt;YSt)V8@.
|@Ab(Y)Y146@ is complemented by @Ts(1Rt;YSt)W19@.
|@Ts(1Lt;YSt)P7@/@Ab(Y)Y146@ males produce large numbers of progeny,
|comparable to wild-type X/Y males.
|@Ts(1Lt;YSt)W27@/@Ab(Y)Y146@ males produce large numbers of progeny,
|comparable to wild-type X/Y males.
|@Ts(1Lt;YSt)V24@/@Ab(Y)Y146@ males show a significant reduction in
|male fertility compared to wild type; 19% of males fail to produce
|any progeny, 46% produce very small numbers of progeny (less than 40/male)
|and only 10% produce more than 80 progeny/male. Postmeiotic defects
|are seen in the testes; spermatid bundles with scattered singular nuclear
|heads are seen frequently, but account only for a small proportion
|of spermatid bundles. Some individualization complexes are located
|away from the nuclear bundles, apparently resulting from caudal movement
|along the tails (as occurs in wild type). Individualised spermatids
|are seen in the basal region of the testes and mature sperm are seen
|in the seminal vesicles.
SYN|Y146
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0029422	CLA 1 Aberration	GSYM 1 Ab(Y)Y2	DT 1 21 Dec 00	RESZ 2516	CLOC 1 h24;h3	REF 1	
ABSY|Ab(Y)Y2
DT|21 Dec 00
SYN|Y2
ID|FBab0029422
REF
{
REFM|FBrf0127362
|Timakov and Zhang
|2000
|-1
}

BPT|h24;h3
MU|&ggr; ray
PRG|Dp(1;Y)B<up>S</up>Yy<up>+</up>
CCM|New order: h1-h24 | h3-h1 (a duplication of h1-h3 and a deletion of
|h25).
MK|B<up>S</up>
OAB|X/@Ab(Y)Y2@/@Dp(1;Y)y<up>+</up>@ males are sterile. Testes show a departure
|from normal development at early postmeiotic stages of spermatid differentiation.
|Before nuclear elongation, round spermatid nuclei begin to fall apart
|in a large number of spermatid bundles, resulting in singular nuclei
|heads that are dispersed throughout the tails. In approximately 10%
|of males, the testes contain exclusively round spermatids scattered
|throughout the length of the tails. Many of the spermatid bundles
|with scattered nuclei are much smaller in diameter than normal, suggesting
|that some of the spermatid tails fail to develop. However, some spermatid
|bundles show aligned nuclear heads associated with individualization
|complexes, as in wild type.
|@C(1;YS)1@/@Ab(Y)Y2@ males are fertile.
|@Ab(Y)Y2@ is complemented by @Ts(1Rt;YSt)V8@.
|@Ts(1Lt;YSt)P7@/@Ab(Y)Y2@, @Ts(1Lt;YSt)W27@/@Ab(Y)Y2@ and @Ts(1Lt;YSt)V24@/@Ab(Y)Y2@
|males produce large numbers of progeny.
REFDSR
{
RDID|FBrf0127362
|Timakov and Zhang
|2000
BPT|h24;h3
MU|&ggr; ray
PRG|Dp(1;Y)B<up>S</up>Yy<up>+</up>
CCM|New order: h1-h24 | h3-h1 (a duplication of h1-h3 and a deletion of
|h25).
MK|B<up>S</up>
OAB|X/@Ab(Y)Y2@/@Dp(1;Y)y<up>+</up>@ males are sterile. Testes show a departure
|from normal development at early postmeiotic stages of spermatid differentiation.
|Before nuclear elongation, round spermatid nuclei begin to fall apart
|in a large number of spermatid bundles, resulting in singular nuclei
|heads that are dispersed throughout the tails. In approximately 10%
|of males, the testes contain exclusively round spermatids scattered
|throughout the length of the tails. Many of the spermatid bundles
|with scattered nuclei are much smaller in diameter than normal, suggesting
|that some of the spermatid tails fail to develop. However, some spermatid
|bundles show aligned nuclear heads associated with individualization
|complexes, as in wild type.
|@C(1;YS)1@/@Ab(Y)Y2@ males are fertile.
|@Ab(Y)Y2@ is complemented by @Ts(1Rt;YSt)V8@.
|@Ts(1Lt;YSt)P7@/@Ab(Y)Y2@, @Ts(1Lt;YSt)W27@/@Ab(Y)Y2@ and @Ts(1Lt;YSt)V24@/@Ab(Y)Y2@
|males produce large numbers of progeny.
SYN|Y2
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027549	CLA 1 Aberration	GSYM 1 Ab(Y;2;3)O-1	DT 1 29 Apr 01	RESZ 389	REF 1	
ABSY|Ab(Y;2;3)O-1
DT|29 Apr 01
SYN|unnamed
ID|FBab0027549
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
}

MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x7@.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027550	CLA 1 Aberration	GSYM 1 Ab(Y;2;3)X2-1	DT 1 29 Apr 01	RESZ 390	REF 1	
ABSY|Ab(Y;2;3)X2-1
DT|29 Apr 01
SYN|unnamed
ID|FBab0027550
REF
{
REFM|FBrf0099191
|Dorer and Henikoff
|1997
|-1
}

MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
REFDSR
{
RDID|FBrf0099191
|Dorer and Henikoff
|1997
MU|X ray
PRG|FBti0016766 == P{lacW}50C.x7
OTH|Enhancement of @w@ variegation from the transgene array @P{lacW}50C.x7@.
SYN|unnamed
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0000078	CLA 1 Aberration	GSYM 1 C(1)94-2A	DT 1 29 Oct 99	RESZ 903	REF 2	
ABSY|C(1)94-2A
DT|29 Oct 99
ID|FBab0000078
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009544
|Novitski and Braver
|1954
|-1
}

NCO|| 1A - 5E | 1F - 1A . 20 - 5E | 1F - 20 |
DIS|Rosenfeld, 1964.
MU|spontaneous \?
PRG|C(1)TR94-2
COR|Possibly X ray induced premeiotically. Apparently arose through an
|asymmetrical or reversed exchange between the 1F region near
|the centromere and the 5E region near the interstitial
|heterochromatin
CCM|Ring shaped in mitotic metaphase.
MK|y<up>1</up>
OTH|Originally heterozygous for @cv<up>1</up>@, @sn<up>1</up>@,
|@v<up>1</up>@, @g<up>1</up>@, and @sd<up>1</up>@.
PHP|Crossing over in region 1F - 6A produces a single ring
|carrying In(1)94-2A = In(1)1F-2A;5E-6A. Reversibly
|convertible to other double-ring configurations by other
|types of exchange (e.g., Novitski and Braver, 1954, Genetics
|39: 197-209).
}
# EOR
ABSR
{
RETE|ID 1 FBab0000079	CLA 1 Aberration	NAM 1 Compound (1) of Armentrout	GSYM 1 C(1)A	DT 1 16 Nov 01	RESZ 2101	SK 29	REF 6	
ABSY|C(1)A
DT|16 Nov 01
NAM|Compound (1) of Armentrout
ID|FBab0000079
REF
{
REFM|FBrf0048950
|Traverse and Pardue
|1988
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0137894
|Letizia et al.
|2001
|-1
REFM|FBrf0128883
|Agudo et al.
|2000
|-1
REFM|FBrf0130123
|Tyler-Smith and Floridia
|2000
|-1
REFM|FBrf0132093
|Abad et al.
|2000
|-1
}

NCO|| 1A - 6F2 | 6F2 - 1A | 20 - 7A1 | 7A1 - 20 . |
DIS|Armentrout, 1964.
MU|spontaneous
PRG|C(1)TR94, y cv v sd . y sn g
COR|Apparently arose by a process
|describable as reversed crossing over in region 6F2 - 7A1.
|Current versions of this chromosome have apparently opened,
|since they are no longer ring-shaped in metaphase. Shown to
|have separated at 13E by Traverse and Pardue (1988, Proc.
|Nat. Acad. Sci. USA 85: 8116-20) such that the new order is
|13E - 7A1 | 7A1 - 20.1 - 6F2 | 6F2 - 1 | 20 - 13E | 13E -
|20.1 - 6F2 | 6F2 - 1 | 20 - 7A1 | 7A1 - 13E which are
|interconvertable by exchange between regions 20 and 13. The
|newly terminal ends at 13E have acquired moderately repeated
|sequences (He-T DNA) ordinarily encountered at telomeres and
|in the chromocenter (Traverse and Pardue). Transmission of
|C(1)A is reduced owing to the fact that half of meiotic
|exchanges lead to the production of dicentric chromosomes.
CCM|Ring shaped in mitotic metaphase.
MK|y<up>1</up>
OTH|Should be the best of all compound-X chromosomes for stock purposes.
|Probably originally heterozygous for @cv<up>1</up>@, @sn<up>1</up>@,
|@v<up>1</up>@, @g<up>1</up>@, and @sd<up>1</up>@.
PHP|An apparently completely stable, compound-ring-X chromosome;
|cannot produce single-X chromosome derivative by
|heterochromatic exchange.
REFDSR
{
RDID|FBrf0048950
|Traverse and Pardue
|1988
OTH|The C(1)A chromosome has spontaneously opened in polytene region 13E
|to produce two new telomeres. Each of the new telomeres has acquired
|HeT-A DNA sequences.
}

SK|FBstBL-4049
|C(1)A, y[1]; T(1;Y;3)W27, y[1] y[+] w[1] f[1] B[S]
|FBstBL-1954
|C(1)A, y[1]/Y & FM0
|FBstBL-3219
|C(1;Y)1, Df(1)g, y[1] f[1] B[1]/C(1)A, y[1]/Dp(1;f)LJ9, y[+] g[+] na[+] Ste[+]
|FBstBL-1879
|Df(1)GE202/Y; Dp(1;2)sn[+]72d/Dp(?;2)bw[D], bw[D] & C(1)A, y[1]/Y; Dp(1;2)sn[+]72d/Dp(?;2)bw[D], bw[D]
|FBstBL-3224
|T(1;Y)E15, y[1] w[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-3158
|T(1;Y)F12, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1848
|T(1;Y)G20, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1] w[1] f[1]
|FBstBL-2474
|T(1;Y)G25, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-3239
|T(1;Y)G8, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-2928
|T(1;Y)N12, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-2575
|T(1;Y)N29, y[1] w[a] Ste[+] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1850
|T(1;Y)N5, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1855
|T(1;Y)P11, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1857
|T(1;Y)R2, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1880
|T(1;Y)R34, y[1] w[1] f[1]: y[+]/C(1)A, y[1]
|FBstBL-1881
|T(1;Y)R38, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1839
|T(1;Y)R44, y[1] w[1] f[1]: B[S]/C(1)A, y[1]
|FBstBL-1864
|T(1;Y)R4, y[1] w[1] f[1]: y[+]/C(1)A, y[1]
|FBstBL-1895
|T(1;Y)S19, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1904
|T(1;Y)S29, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1913
|T(1;Y)T16, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1912
|T(1;Y)T9, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-3060
|T(1;Y)V24, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1915
|T(1;Y)V43, y[1] w[1] Ste[+] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1922
|T(1;Y)V63, y[1] w[1] Ste[+] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-478
|T(1;Y)V8, y[1] w[1]: y[+] B[S]/Dp(1;Y)V8, y[+] & C(1)A, y[1]/Dp(1;Y)V8, y[+]
|FBstBL-2950
|T(1;Y)W19, y[1] w[1] f[1]: y[+] B[S]/C(1)A, y[1]
|FBstBL-1449
|Ts(1Lt;Y)E5, y[1] w[1] f[1]: y[+] & C(1)A, y[1]/0
|FBstBL-4621
|y[1] w[1] ec[1] s[1] f[1]/C(1)A, y[1]
SKC|29
}
# EOR
ABSR
{
RETE|ID 1 FBab0000080	CLA 1 Aberration	NAM 1 Compound (1) Double X	GSYM 1 C(1)DX	DT 1 22 Aug 04	RESZ 3668	ALESR 1	SK 335	REF 18	
ABSY|C(1)DX
DT|22 Aug 04
SYN|Compound-1 DX
|:=
NAM|Compound (1) Double X
ID|FBab0000080
REF
{
REFM|FBrf0174706
|Niemi et al.
|2004
|-1
REFM|FBrf0111904
|Helms et al.
|1999
|-1
REFM|FBrf0141717
|Carvalho et al.
|2001
|-1
REFM|FBrf0174705
|Simmons et al.
|2004
|-1
REFM|FBrf0127410
|Zakharenko et al.
|2000
|-1
REFM|FBrf0052612
|Prudhommeau and Proust
|1990
|-1
REFM|FBrf0127332
|Skaer and Simpson
|2000
|-1
REFM|FBrf0098381
|The Moscow Regional Drosophila melanogaster Stock Center
|Dubna
|-1
REFM|FBrf0095657
|Mason et al.
|1997
|-1
REFM|FBrf0007401
|Valencia et al.
|1949
|-1
REFM|FBrf0045718
|Zhimulev et al.
|1987
|-1
REFM|FBrf0005925
|Muller
|1943
|-1
REFM|FBrf0132437
|Green and Piergentili
|2000
|-1
REFM|FBrf0141259
|Bloomington Drosophila Stock Center
|
|-1
REFM|FBrf0082182
|Jang et al.
|1995
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0145107
|Hunter et al.
|2002
|-1
REFM|FBrf0056147
|Birchler
|1992
|-1
}

DIS|Muller.
MU|X ray
PRG|In(1)dl-49, y<up>1</up> w<up>1</up> f<up>1</up>/In(1)sc<up>8</up>, sc<up>8</up> B<up>1</up>
CCM|C(1)DX, In(1)dl-49 - In(1)sc<up>8</up>., y f - y<up>-</up> sc<up>8</up> f..
AMD|bb
BIP|4D7--E1;11F2--4 (from In(1)dl-49)
MK|y<up>1</up> f<up>1</up>
OAB|Oocytes from All-Compound females produce anaphase I and meiosis II figures 64% of the time, i.e. they have bypassed metaphase I arrest.
OTH|female [stated by Muller to have been
|In(1)dl-49/In(1)sc<up>8L</up>y<up>3PR</up>, but the derivative does not
|carry y<up>3P</up>]. Was originally y<up>1</up> w<up>1</up> f<up>1</up> - y<up>-</up> sc<up>8</up> B<up>1</up> ., but by
|double exchange f<up>1</up> became homozygous and B<up>1</up> was lost.
|@y<up>1</up>@, @w<up>1</up>@, @f<up>1</up>@ versions exist.
PHP|A reversed acrocentric heterozygous for In(1)dl-49; it is
|useful in balancing because it is very stable, which is
|probably due to little interstitial heterochromatin. y w f
|detachments very rarely produced. Also produces a low
|incidence of homozygosis for w.
|C(1)DX/0 lethal
REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
OTH|Attached X chromosomes homozygous for various @w@ alleles were used
|to study dosage compensation of @w@.
}

REFDSR
{
RDID|FBrf0082182
|Jang et al.
|1995
OAB|Oocytes from All-Compound females produce anaphase I and meiosis II figures 64% of the time, i.e. they have bypassed metaphase I arrest.
OTH|A study of metaphase arrest found that crossovers between homologs
|attached to the same centromere do not induce metaphase arrest. Hence
|exchanges induce metaphase arrest only when they physically conjoin
|two separate kinetochores. The signal that mediates metaphase arrest
|is not the exchange event per se, but the resulting tension on homologous
|kinetochores.
}

REFDSR
{
RDID|FBrf0098381
|The Moscow Regional Drosophila melanogaster Stock Center
|Dubna
MK|y<up>1</up> f<up>1</up>
OTH|Some versions also marked with @w<up>1</up>@.
}

REFDSR
{
RDID|FBrf0127332
|Skaer and Simpson
|2000
SYN|Compound-1 DX
}

BGV
{
BGVSY|C(1)DX-P
ID|FBba0000076
OTH|Carries @P-element@s derived from &pgr;2.
REF|FBrf0141259
SK|FBstBL-3493
|y[1] v[1] Rst(1)JH[A3]/C(1)DX-P/Dp(1;Y)y[+] <P>
}

SK|FBstBL-10
|amx[1] lz[g] v[1]/C(1)DX, y[1] f[1]
|FBstBL-12
|bi[1] ct[6] g[2]/C(1)DX, y[1] f[1]
|FBstBL-3233
|Binscy/C(1)DX, y[1] f[1]/Dp(1;Y)y[+]
|FBstBL-4354
|Binscy, w[1]/C(1)DX, y[1] f[1]
|FBstBL-17
|Bx[3]/C(1)DX, y[1] w[1] f[1]
|FBstBL-4260
|C(1)DX, y[1] f[1]; bw[1]; e[4]; ci[1] ey[R]
|FBstBL-6503
|C(1)DX, y[1] f[1]; Caps[BJ]/In(4)ci[D], ci[D] pan[ciD]
|FBstBL-4242
|C(1)DX, y[1] f[1]/Dp(1;Y)y[+]; ca[1] awd[K]
|FBstBL-3721
|C(1)DX, y[1] f[1]/FM6; ry[506]
|FBstBL-4040
|C(1)DX, y[1] f[1]/In(1)dl-49, w[1] lz[s]
|FBstBL-4338
|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]
|FBstBL-4069
|C(1)DX, y[1] f[1]/lz[BS+46] ras[4] v[1]
|FBstBL-2527
|C(1)DX, y[1] f[1]/pch[2] y[1]/Dp(1;Y)y[+]; sv[spa-pol]
|FBstBL-4045
|C(1)DX, y[1] f[1]/R(1)2, B[1]/Dp(1;Y)y[+]; Dp(?;2)bw[D], bw[D]
|FBstBL-3838
|C(1)DX, y[1] f[1]/R(1)2, In(1)sc[8], Df(1)ac, ac[1] sc[8] w[a] B[1]/Dp(1;Y)y[+]
|FBstBL-4050
|C(1)DX, y[1] f[1]/R(1)2, y[1] f[1]/Dp(1;Y)y[+]; st[1] mus302[*]
|FBstBL-4054
|C(1)DX, y[1] f[1]/R(1)5, In(1)w[m4]; T(1;4)w[m258-18], y[1]
|FBstBL-2540
|C(1)DX, y[1] f[1]; ry[506] P{ry[+t7.2]=Delta2-3}99B
|FBstBL-3896
|C(1)DX, y[1] f[1]/Sxl[f1] oc[1] ptg[1] v[1]
|FBstBL-4055
|C(1)DX, y[1] f[1]; T(1;4)sc[H], sc[H]
|FBstBL-4056
|C(1)DX, y[1] f[1]; T(1;4)Sidky
|FBstBL-4057
|C(1)DX, y[1] f[1]; T(1;4)w[m258-18]
|FBstBL-7368
|C(1)DX, y[1] f[1]/v[1] f[3N] car[1]
|FBstBL-1488
|C(1)DX, y[1] v[1] & C(1;Y)*, shi[1] y[1] v[1] bb[1]
|FBstBL-3922
|C(1)DX, y[1] w[1] f[1]/Df(1)y74k24.1, RpL36[y74k24.1]/Dp(1;Y)y[2]61l
|FBstBL-4058
|C(1)DX, y[1] w[1] f[1]; T(1;4)B[S], B[S]
|FBstBL-13383
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG00162/C(1)DX, y[1] f[1]; ry[506]
|FBstBL-13388
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}sni[KG00373]/C(1)DX, y[1] f[1]; ry[506]
|FBstBL-1608
|C(1;Y)2, y[1] ct[6] f[1] & C(1)DX, y[1] f[1]
|FBstBL-82
|C(1;Y)7, y[1] v[1] bb[-]: bb[-]/Dp(1;f)1185/C(1)DX, y[1] w[a]
|total=
|334
SKC|335
}
# EOR
ABSR
{
RETE|ID 1 FBab0023961	CLA 1 Aberration	GSYM 1 C(1)FMA4	DT 1 12 Nov 00	RESZ 541	REF 1	
ABSY|C(1)FMA4
DT|12 Nov 00
ID|FBab0023961
REF
{
REFM|FBrf0040979
|Ganetzky
|1984
|-1
}

BIP|3C2;h28 (from In(1)w<up>m4</up>)
PRG|In(1)w<up>m4</up>
|In(1)FM7
COR|The @In(1)w<up>m4</up>@ progenitor has accumulated an undefined additional
|aberration.
REFDSR
{
RDID|FBrf0040979
|Ganetzky
|1984
PRG|In(1)w<up>m4</up>
|In(1)FM7
COR|The @In(1)w<up>m4</up>@ progenitor has accumulated an undefined additional
|aberration.
OTH|The @In(1)FM7@ chromosome is marked with @y<up>2</up>@ and @bb@<up>-</up>.
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0000081	CLA 1 Aberration	NAM 1 Compound (1) Multiple	GSYM 1 C(1)M2	DT 1 12 Nov 00	RESZ 517	REF 2	
ABSY|C(1)M2
DT|12 Nov 00
SYN|FMA2: First Multiple Attached
NAM|Compound (1) Multiple
ID|FBab0000081
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0063641
|Lewis
|1958
|-1
}

DIS|Lewis, Aug. 1954.
MU|X ray
PRG|In(1)sc<up>7</up> + In(1)AM
|In(1)FM4
COR|exchange of the proximal heterochromatin of In(1)sc<up>7</up> + AM and the distal heterochromatin of In(1)FM4
CCM|C(1)M2, In(1)sc<up>7</up>+ AM - In(1)FM4., sc<up>7</up> - y<up>-</up> sc<up>8</up> dm B..
BIP|3C;4E--F (from In(1)FM4)
}
# EOR
ABSR
{
RETE|ID 1 FBab0000082	CLA 1 Aberration	GSYM 1 C(1)M3	DT 1 12 Nov 00	RESZ 523	SK 17	REF 3	
ABSY|C(1)M3
DT|12 Nov 00
SYN|FMA3
ID|FBab0000082
REF
{
REFM|FBrf0086407
|Francis-Lang et al.
|1996
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0063641
|Lewis
|1958
|-1
}

DIS|Lewis, Feb. 1955.
MU|recombination
PRG|In(1)sc<up>7</up>
|C(1)M2, y<up>2</up>
COR|exchange within In(1)AM element of C(1)M2 in triploid
CCM|C(1)M3, In(1)AM - In(1)FM4., y<up>2</up> - y<up>-</up> sc<up>8</up> dm B..
BIP|1B4;6D8 (from In(1)sc<up>7</up>)
PHP|Detachment rare; useful in balancing.
SK|FBstBL-3509
|C(1)M3; Ubx[bx-3] abd-A[Hab-1] Abd-B[Mc]/TM1
|FBstBL-1018
|C(1)M3, y[1]/Dp(1;Y)y[+]; P{ry[+t7.2]=A92}tsh[i71]; ca[1] awd[K]
|FBstBL-1296
|C(1)M3, y[1]/Dp(1;Y)y[+]; P{w[+tAR] ry[+t7.2AR]=wA[R]}tsh[4-3]; awd[K]
|FBstBL-1139
|C(1)M3, y[2]/0; CyO/T(2;3)ap[Xa] & C(1;Y)1, y[1]: y[+]/0; CyO/T(2;3)ap[Xa], ap[Xa]
|FBstBL-1993
|C(1)M3, y[2] bb[1]/Dp(1;Y)y[+]; Df(3R)A/TM6 & C(1;Y)*, y[1]/Dp(1;Y)y[+]; Df(3R)A/TM6
|FBstBL-1641
|C(1)M3, y[2]; Dp(2;1)G146, sn[3]: pal[1] Bl[1]/CyO
|FBstBL-1780
|C(1)M3, y[2]; ru[1] h[1] st[1] p[p] ss[1] e[s]
|FBstBL-937
|Df(1)N-71h/C(1)M3, y[2]; Dp(1;2)51b/+
|FBstBL-6348
|Df(1)sc[8], w[a]/C(1)M3, y[2]; Dp(1;3)sc[J4], y[+], jv[1]
|FBstBL-6349
|Df(1)sc[8], w[a]/C(1)M3, y[2]; Dp(1;3)sc[J4], y[+], mwh[1] jv[1]/TM1
|FBstBL-1992
|Df(3R)A/Dp(3;3)Tpl; C(1)M3, y[2] bb[*]/C(1;Y)2, y[1]
|FBstBL-2934
|Df(3R)Tpl9/Dp(3;3)Tpl; C(1)M3, y[2] bb[*]/C(1;Y)*
|FBstBL-666
|e(S)X[1]/C(1)M3, y[2]; al[1] S[1] ast[1] dpp[d-ho]/SM1
|FBstBL-1304
|In(1)w[m4], In(1)AB, y[2]/C(1)M3
|FBstBL-1809
|T(Y;3)Antp[Ns-rv3], Antp[Ns-rv3] H[1]/C(1)M3, y[2]/TM6
|FBstBL-4153
|y[1] cho[*] (w[*] B[1]) Zw[n1]/C(1)M3, y[2] bb[-]; Cy[1]/?
|FBstBL-681
|y[2] z[ae(bx)2] w[bf]/C(1)M3, y[2]; Sb[sbd-2] ss[1] Ubx[bx-34e]/TM1
SKC|17
}
# EOR
ABSR
{
RETE|ID 1 FBab0000083	CLA 1 Aberration	GSYM 1 C(1)M4	DT 1 17 Oct 03	RESZ 1219	SK 41	REF 5	
ABSY|C(1)M4
DT|17 Oct 03
ID|FBab0000083
REF
{
REFM|FBrf0159638
|Presgraves et al.
|2003
|-1
REFM|FBrf0026093
|Craymer
|1974
|-1
REFM|FBrf0144851
|Schotta et al.
|2002
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0127307
|Sawamura et al.
|2000
|-1
}

DIS|Craymer, May 1972.
MU|X ray
PRG|In(1)w<up>m4</up> + In(1)AB
|In(1)FM7
COR|exchange of the proximal heterochromatin of In(1)w<up>m4</up> + AB and the distal heterochromatin of FM7
CCM|C(1)M4, In(1)w<up>m4</up> + AB - FM7., y w<up>m4</up> - y<up>-</up> w<up>a</up> v<up>Of</up> sc<up>8</up>..
PED|position-effect variegation for: w
OTH|Useful in maintenance of XY-bearing stocks without a free Y.
|Some derivatives are marked with @y<up>2</up>@ @bb@<up>-</up>.
PHP|Because of the w<up>m4</up>/w<up>a</up> constitution, C(1)M4 females
|without a Y chromosome display strong variegation, those
|with YS moderate variegation and those with YL or a complete
|Y almost no variegation.
|Detachment rate
|approximately 1/15,000. A powerful enhancer of autosomal
|recombination, but has low viability in combination with
|autosomal rearrangements.
SK|FBstBL-1999
|C(1)M4, y[2]/C(1;Y)6, w[1118]
|FBstBL-2550
|C(1)M4, y[2]/ct[n] oc[1] Hmr[1] v[1]
|FBstBL-1249
|C(1)M4, y[2]; In(3L)C90[L]P[R], In(3R)Ubx[P18], Ubx[1] Ubx[P18] e[4]/In(3L)P[L]C90[R], Hn[r] h[1] app[1]
|FBstBL-1204
|C(1)M4, y[2]; In(3L)P, rs[2] th[1]
|FBstBL-1451
|C(1)M4, y[2]; In(3LR)206/In(3R)Hu, Antp[Hu] Sb[Spi]
|FBstBL-1320
|C(1)M4, y[2]; In(3LR)230/th[1] st[1] cp[1] in[1] kni[ri-1] Kg[V] Ki[1] p[p]
|FBstBL-3073
|C(1)M4, y[2]; In(3LR)A114/Sb[1] Ubx[1]
|FBstBL-1435
|C(1)M4, y[2]; In(3LR)B158/In(3LR)Ubx[16R], th[1] st[1] cp[1] Ubx[R16]
|FBstBL-1193
|C(1)M4, y[2]; In(3LR)bxd[194L]79i[R], p[p]/In(3LR)79i[L]bxd[194R], p[p]
|FBstBL-1456
|C(1)M4, y[2]; In(3LR)bxd[194L]C190[R], p[p]/In(3LR)C190[L]bxd[194R], p[p]
|FBstBL-1297
|C(1)M4, y[2]; In(3LR)C190[L]A114[R]/In(3LR)A114[L]Ubx[101R], th[1] st[1], kni[ri-1]
|FBstBL-1186
|C(1)M4, y[2]; In(3LR)HR33, In(3LR)LD6, ru[1] h[1] Sb[sbd-2]
|FBstBL-1390
|C(1)M4, y[2]; In(3LR)P42, st[1] cp[1] in[1] kni[ri-1]
|FBstBL-1216
|C(1)M4, y[2]; LS(2)SM1, In(2R)bw[V57e]//DS(2)SM1, In(2L)Cy, Cy[1]
|FBstBL-1198
|C(1)M4, y[2]; LS(3)HR33, In(3LR)LD6, In(3L)HR27, In(3LR)P42, In(3LR)224, st[1] Sb[sbd-2]//DS(3)HR33 + In(3LR)LD6, In(3L)HR15, In(3L)HR27, In(3LR)P42, In(3LR)224, st[1] Sb[sbd-2]
|FBstBL-1440
|C(1)M4, y[2]; LS(3)Ubx[42T], D[3]//DS(3)Ubx[42T]
|FBstBL-1633
|C(1)M4, y[2]; p[p]
|FBstBL-1179
|C(1)M4, y[2]/shi[1]; In(3LR)224, ru[1]
|FBstBL-1170
|C(1)M4, y[2]/shi[1]; In(3LR)225/TM3, Sb[1]
|FBstBL-1172
|C(1)M4, y[2]/shi[1]; In(3LR)230/th[1] st[1] cp[1] in[1] kni[ri-1] Kg[V] Ki[1] p[p]
|FBstBL-1177
|C(1)M4, y[2]/shi[1]; In(3LR)234
|FBstBL-1175
|C(1)M4, y[2]/shi[1]; In(3LR)C190/Sb[1]
|FBstBL-1330
|C(1)M4, y[2]/shi[1]; or[1] Kr[If-1]; Sb[1]/In(3R)Ubx[80], Ubx[80]
|FBstBL-1173
|C(1)M4, y[2]/shi[1]; (st[1]) in[1] kni[ri-1] p[p]
|FBstBL-1408
|C(1)M4, y[2]; th[1] st[1] cp[1] in[1] kni[ri-1] Kg[V] Ki[1] p[p]/TM3, Sb[1] Ser[1]
|FBstBL-1289
|C(1)M4, y[2]; TM6B, Tb[1] Dr[Mio]/In(3R)Dl[B], Dl[B]
|FBstBL-2000
|C(1)M4, y[2]/Y & C(1;Y)6, w[1118]/Y
|FBstBL-1394
|C(1;Y)1, In(1)dl-49, y[1] pn[62] v[Of] f[1]/0/C(1)M4
|FBstBL-995
|C(1;Y)3, In(1)FM7, w[1] m[2]/0/C(1)M4, y[2]
|FBstBL-1398
|C(1;Y)6, Dp(3;1)P115, y[2] sc[1] su(s)[2] pn[1] sn[3], y[+]/0 & C(1)M4, y[1]
|total=
|41
SKC|41
}
# EOR
ABSR
{
RETE|ID 1 FBab0028738	CLA 1 Aberration	GSYM 1 C(1)M5	DT 1 13 Sep 99	RESZ 132	SK 2	REF 1	
ABSY|C(1)M5
DT|13 Sep 99
ID|FBab0028738
REF
{
REFM|FBrf0109188
|Florence
|1999.7.22
|-1
}

SK|FBstBL-5281
|Df(1)dx81, w[*]/Dp(1;Y)dx[+]1/C(1)M5
|FBstBL-5279
|Df(1)JC70/Dp(1;Y)dx[+]5, y[+]/C(1)M5
SKC|2
}
# EOR
ABSR
{
RETE|ID 1 FBab0000084	CLA 1 Aberration	NAM 1 Compound (1) of Novitski and Braver	GSYM 1 C(1)NB	DT 1 22 Aug 04	RESZ 862	REF 2	
ABSY|C(1)NB
DT|22 Aug 04
NAM|Compound (1) of Novitski and Braver
ID|FBab0000084
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009544
|Novitski and Braver
|1954
|-1
}

DIS|Novitski and Braver.
MU|recombination
PRG|In(1)EN
|In(1)dl-49
COR|exchange between the heterochromatic short arm of In(1)EN and the proximal heterochromatin of In(1)dl-49
CCM|C(1)NB, In(1)dl-49.In(1)sc<up>4L</up>EN<up>R</up>; originally y v f
|car . y m; In(1)dl-49 and In(1)EN attached proximally to a
|single centromere.
|Essentially a tandem metacentric heterozygous for @In(1)dl-49@.
|Can exist in a number of different configurations interconvertible by
|crossing over.
BIP|1A;20F;20F (from In(1)EN)
|4D7--E1;11F2--4 (from In(1)dl-49)
PHP|Generates single rings at different frequencies, depending on
|configuration of the compound.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000085	CLA 1 Aberration	NAM 1 Compound (1) Reversed Acrocentric	GSYM 1 C(1)RA	DT 1 12 Nov 00	RESZ 1884	SK 7	REF 5	
ABSY|C(1)RA
DT|12 Nov 00
SYN|RA
NAM|Compound (1) Reversed Acrocentric
ID|FBab0000085
REF
{
REFM|FBrf0011855
|Sandler
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009543
|Novitski
|1954
|-1
REFM|FBrf0009563
|Sandler
|1954
|-1
REFM|FBrf0033196
|Sandler and O'Tousa
|1979
|-1
}

DIS|Novitski.
MU|spontaneous
|recombination
PRG|C(1;YL)1
|In(1)sc<up>8</up>
COR|between the proximal heterochromatin of X.YL and the distal
|heterochromatin of In(1)sc<up>8</up> or possibly by sister-strand
|union in one of the heterochromatic segments followed by a
|normal euchromatic exchange. A frequently recurring event
|that seems to require the presence of YL. More recent
|attempts to repeat such constructions have been
|unsuccessful, except in response to X-irradiation.
CCM|C(1)RA, + - In(1)sc<up>8</up>..
BIP|1B2;h32 (from In(1)sc<up>8</up>)
PHP|Yields frequent detachments resulting from exchange between
|the Y chromosome and the interstitial heterochromatin of the
|reversed acrocentric and preferential recovery of the
|proximal X. Tetrad distribution usually quite abnormal;
|one-exchange tetrads infrequent and no- and two-exchange
|tetrads frequent. Exchange frequency increased by addition
|of Y or y<up>+</up>YL, but tetrad distribution remains abnormal
|(Sandler, 1954). YL appended as a second arm to C(1)RA
|normalizes tetrad distribution (Sandler, 1958). Tetrad
|distribution is normal in more recently recovered C(1)RA
|chromosomes (Sandler and O'Tousa, 1979), reason for differences
|between 1954 and 1979 data is unclear. The presence of a Y
|chromosome or a free-X duplication as a homologue markedly
|increases both exchange between the elements of the compound
|and fecundity of compound-bearing females.
SK|FBstBL-1305
|C(1)RA, cin[1] y[1]/Dp(1;Y)y[+]/cin[1] y[1] w[1]
|FBstBL-4554
|C(1)RA, cin[1] y[1]/Dp(1;Y)y[+]/Sxl[K1274-1] v[24]
|FBstBL-3923
|C(1)RA, In(1)AB, y[1], In(1)sc[8], sc[8]/Dp(1;YL)sc[S1]/C(1;Y)1, y[1] B[1]
|FBstBL-3220
|C(1)RA, In(1)sc[J1], In(1)sc[8], l(1)1Ac[1], sc[J1] sc[8]/C(1;Y)6, Df(1)259, w[1]/Dp(1;Y)y[53i], y[53i] sc[8]
|FBstBL-3924
|C(1)RA, v[1] f[1]/C(1;YL)C2, y[1] cv[1] v[1] f[1] car[1] bb[-]/C(YS)1
|FBstBL-4486
|C(1)RA, y[1]: In(1)sc[8], sc[8]/Dp(1;YL)y[+]YL/C(1;Y)1, y[1] B[1]
|FBstBL-3925
|Dp(1;f)1173; C(1)RA, Df(1)259, y[1]/C(1;Y)6, Df(1)259, y[1] w[1]
SKC|7
}
# EOR
ABSR
{
RETE|ID 1 FBab0000086	CLA 1 Aberration	GSYM 1 C(1)RA60g	DT 1 04 Nov 98	RESZ 961	SK 3	REF 4	
ABSY|C(1)RA60g
DT|04 Nov 98
SYN|XX,Df(1)60g
ID|FBab0000086
REF
{
REFM|FBrf0063713
|Mohler
|1960
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0018685
|Gethmann
|1967
|-1
REFM|FBrf0063456
|Gethmann
|1967
|-1
}

DIS|Mohler, July 1960.
MU|spontaneous
COR|A spontaneous euchromatic event (perhaps sister chromatid union)
|a triploid female heterozygous for In(1)sc<up>8</up>+dl-49
CCM|C(1)RA60g, + - In(1)sc<up>8</up>.
|Deleted for interstitial heterochromatin of X.
|Deleted for proximal euchromatin of X.
AMD|su(f)
OAB|Requires a duplication carrying @su(f)@ and @bb@ in order to survive.
OTH|The reciprocal exchange product, Dp(1;f)60g, recovered from
|same fly.
PHP|Exhibits standard distribution of tetrads in meiosis
|(Gethmann).
REFDSR
{
RDID|FBrf0063456
|Gethmann
|1967
SYN|XX,Df(1)60g
}

REFDSR
{
RDID|FBrf0063713
|Mohler
|1960
MU|spontaneous
SYN|XX,Df(1)60g
}

SK|FBstBL-2170
|C(1)RA60g, y[1] B[1] w[a]/FM7c/Dp(1;Y)su(f)[+]
|FBstBL-2153
|Dp(1;f)60g, y[31d]/C(1)RA60g/y[1] ac[Hw-1] g[2] f[1]
|FBstBL-2164
|Dp(1;f)65X[C2], y[+]/C(1)RA60g/C(1;Y)*, y[1] v[1] f[1] car[1]
SKC|3
}
# EOR
ABSR
{
RETE|ID 1 FBab0000087	CLA 1 Aberration	GSYM 1 C(1)RA85	DT 1 21 Feb 95	RESZ 635	REF 2	
ABSY|C(1)RA85
DT|21 Feb 95
ID|FBab0000087
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0048200
|Mount et al.
|1988
|-1
}

MU|spontaneous
|recombination
PRG|In(1)sc<up>S1L</up>sc<up>8R</up> + In(1)S, w<up>a</up> B y w<up>1118</up> f<up>5</up>
COR|between the proximal heterochromatin of y w<up>1118</up> f<up>5</up> and the distally inverted heterochromatin of Basc, with subsequent loss of B and homozygosis of f<up>5</up>
CCM|C(1)RA85, y w<up>1118</up> f<up>5</up> - In(1)sc<up>S1L</up> sc<up>8R</up> +S, y<up>-</up>
|sc<up>8</up> w<up>r</up> f<up>5</up>.
PHP|A stable compound X chromosome.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000088	CLA 1 Aberration	NAM 1 Compound (1) Reversed Metacentric	GSYM 1 C(1)RM	DT 1 22 Aug 04	RESZ 3157	ALESR 1	SK 354	REF 17	
ABSY|C(1)RM
DT|22 Aug 04
SYN|Attached-X
|A-X
|attached-X
|.=
NAM|Compound (1) Reversed Metacentric
ID|FBab0000088
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0108616
|Bloomington Drosophila Stock Center
|1999.7.1
|-1
REFM|FBrf0152012
|Dauwalder et al.
|2002
|-1
REFM|FBrf0098381
|The Moscow Regional Drosophila melanogaster Stock Center
|Dubna
|-1
REFM|FBrf0056104
|Rose and Wieschaus
|1992
|-1
REFM|FBrf0132437
|Green and Piergentili
|2000
|-1
REFM|FBrf0023530
|Leigh
|1972
|-1
REFM|FBrf0010234
|Welshons
|1955
|-1
REFM|FBrf0095657
|Mason et al.
|1997
|-1
REFM|FBrf0003106
|Beadle and Emerson
|1935
|-1
REFM|FBrf0004291
|Morgan
|1938
|-1
REFM|FBrf0001148
|Morgan
|1922
|-1
REFM|FBrf0004154
|Morgan
|1938
|-1
REFM|FBrf0089627
|Dernburg et al.
|1996
|-1
REFM|FBrf0073960
|Moore et al.
|1994
|-1
REFM|FBrf0056147
|Birchler
|1992
|-1
REFM|FBrf0001401
|Anderson
|1925
|-1
}

DIS|L. V. Morgan, 12th Feb. 1921.
MU|recombination
COR|Recurs regularly by exchange between the heterochromatin of the short
|arm of one X, XYS, or XYL that of the base of the long arm of a sister
|or homolog. Can
|be induced in mature X.YL -bearing sperm (Leigh, 1972, DIS
|48: 107). Presumably the pericentric heterochromatic
|constitutions of independently arising C(1)RM chromosomes varies.
CCM|C(1)RM, +.+; two X chromosomes in normal sequence attached
|proximally to the same centromere
MK|f<up>1</up> mal<up>2</up>
OTH|Exists with many combinations of markers.
PHP|Recombination with the Y chromosome leads to detachments
|with a frequency of about 10<up>-3</up> in C(1)RM/Y females. Has
|been extensively used in studies of crossing over (e.g.,
|Anderson, 1925, Genetics 10: 403-17; Beadle and Emerson,
|1935, Genetics 20: 192-206; Welshons, 1955, Genetics 40:
|918-36).
REFDSR
{
RDID|FBrf0004291
|Morgan
|1938
SYN|Attached-X
}

REFDSR
{
RDID|FBrf0056147
|Birchler
|1992
OTH|Attached X chromosomes homozygous for various @w@ alleles were used
|to study dosage compensation of @w@.
}

REFDSR
{
RDID|FBrf0098381
|The Moscow Regional Drosophila melanogaster Stock Center
|Dubna
MK|f<up>1</up> mal<up>2</up>
}

REFDSR
{
RDID|FBrf0132437
|Green and Piergentili
|2000
SYN|A-X
|attached-X
}

BGV
{
BGVSY|C(1)RM-w<up>+</up>8
ID|FBba0000291
REF|FBrf0108616
REFDSR
{
RDID|FBrf0108616
|Bloomington Drosophila Stock Center
|1999.7.1
MK|y<up>1</up> w<up>*</up>
|Ecol\lacZ<up>3-76</up> Ecol\lacZ<up>5-45fD</up> Ecol\lacZ<up>P\T.W</up>
TRNA|FBti0001034 == P{lacW}5-45fD
|FBti0001033 == P{lacW}4-5fP
|FBti0001031 == P{lacW}3-52d
|FBti0001032 == P{lacW}3-76a
}

}

SK|FBstBL-4093
|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]
|FBstBL-4488
|C(1)RM, sc[1] v[1] f[1]/C(1;YS)1, f[1]/Df(YS)st
|FBstBL-3959
|C(1)RM, sc[1] v[1] f[1]/R(YL)/C(1;YS)6, In(1)EN2, w[1] oc[1] ptg[1] f[1]
|FBstBL-4489
|C(1)RM, y[1]/C(1;YL)1, y[1] cv[1] v[1] f[1] car[1]/C(YS)1
|FBstBL-1217
|C(1)RM, y[1] pn[1] v[1]/0 & C(1;Y)*, y[1] B[1]/0
|FBstBL-4248
|C(1)RM, y[1] pn[1] v[1]/C(1;Y)1, y[1] B[1]/0; sv[spa-pol]
|FBstBL-3697
|C(1)RM, y[1] P{w[+mC]=lacW}5-45fD w[*] P{lacW}4-5fP P{lacW}3-52d P{lacW}3-76a/+
|FBstBL-16
|C(1)RM, y[1] P{w[+mC]=lacW}5-45fD w[*] P{lacW}4-5fP P{lacW}3-52d P{lacW}3-76a/0/C(1;Y)13, v[1] f[1]
|FBstBL-3711
|C(1)RM, y[1] P{w[+mC]=lacW}5-45fD w[*] P{lacW}4-5fP P{lacW}3-52d P{lacW}3-76a/w[1118]/Y
|FBstBL-4485
|C(1)RM, y[1] sc[1] t[2] v[1] f[1] car[1]/C(1;Y)1, y[1] y[+] w[1] sn[5] oc[1] ptg[1] v[1]/0
|FBstBL-3758
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)110-8, y[2] y[+] su(w[a])[1] w[a]
|FBstBL-3752
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)129-16, y[2] y[+] su(w[a])[1] w[a]
|FBstBL-1612
|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
|FBstBL-4494
|C(1)RM, y[1] v[1] bb[-]/C(1;Y)112-17, y[2] su(w[a])[1] w[a]/0
|FBstBL-4490
|C(1)RM, y[1] v[1] f[1]/Dp(1;1)L-B[S] Df(1)bb3a, y[1] cv[1] v[1] f[1] B[S] bb[-]
|FBstBL-3969
|C(1)RM, y[1] v[1] f[1]/R(YL)/C(1;YS)1
|FBstBL-1141
|C(1)RM, y[2] sc[1] z[1]/T(1;3)m9, dsx[D] Sb[1] e[1] l(3)e[1]
|FBstBL-3807
|C(1)RM, y[2] su(w[a])[1] w[a] 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]
|FBstBL-3934
|C(1)RM, y[2] su(w[a])[1] w[a] bb[-]/R(YL)/C(1;YS)6, In(1)EN2, oc[1] ptg[1] f[1]
|FBstBL-5952
|C(1;Y)108-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
|FBstBL-5953
|C(1;Y)115-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
|FBstBL-2548
|C(1;Y)1, y[1] cv[1] B[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2549
|C(1;Y)1, y[1] cv[1] v[1] B[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-5128
|C(1;Y)1, y[1] sn[3] l(1)dd4[1]/C(1)RM, y[1] v[1]; Dp(1;f)LJ9, y[+]
|FBstBL-2556
|C(1;Y)1, y[1] v[1] f[1] B[1]: y[+]/0 & C(1)RM, y[1] v[1]/0
|FBstBL-700
|C(1;Y)1, y[1] v[1] f[1] B[1]: y[+]/C(1)RM, y[2] su(w[a])[1] w[a]
|FBstBL-2494
|C(1;Y)1, y[1] w[A738]: y[+]/0 & C(1)RM, y[1] v[1]/0
|FBstBL-2454
|C(1;Y)2, B[S], y[1] ct[6] f[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2501
|C(1;Y)2, B[S], y[1] v[1] bb[-]/0 & C(1)RM, y[1] v[1] bb[-]
|FBstBL-2486
|C(1;Y)2, y[+]/0 & C(1)RM, y[1] v[1]/0
|total=
|354
SKC|354
}
# EOR
ABSR
{
RETE|ID 1 FBab0000089	CLA 1 Aberration	NAM 1 Compound (1) Reversed Ring	GSYM 1 C(1)RR1	DT 1 16 Jun 98	RESZ 447	REF 2	
ABSY|C(1)RR1
DT|16 Jun 98
SYN|RR
NAM|Compound (1) Reversed Ring
ID|FBab0000089
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009543
|Novitski
|1954
|-1
}

DIS|Zimmering.
MU|spontaneous
PRG|C(1)TR1
CCM|C(1)RR1, + - In(1)EN, y<up>-</up> sc<up>-</up> - y; two X chromosomes
|attached by their normally distal ends to a common
|centromere and by their normally proximal ends to each
|other.
MK|y<up>1</up>
}
# EOR
ABSR
{
RETE|ID 1 FBab0000090	CLA 1 Aberration	GSYM 1 C(1)RR2	DT 1 04 Nov 98	RESZ 902	REF 3	
ABSY|C(1)RR2
DT|04 Nov 98
ID|FBab0000090
REF
{
REFM|FBrf0011855
|Sandler
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0011393
|Sandler
|1957
|-1
}

DIS|Sandler.
MU|X ray
PRG|C(1)RM, In(1)sc<up>8</up>, In(1)sc<up>S1L</up>EN<up>R</up>
COR|Recovered as simultaneous loss of y<up>+</up> from the
|tip of both arms.
CCM|C(1)RR2, In(1)sc<up>8</up>.In(1)sc<up>S1L</up>EN<up>R</up>; originally y<up>-</up> cv v
|f . y m car. In(1)sc<up>8</up> and In(1)sc<up>S1L</up>EN<up>R</up> attached
|proximally to a single centromere and distally at their
|distal heterochromatic segments.
PHP|Tetrad distribution abnormal; one-exchange tetrads are
|infrequent and no- and two-exchange tetrads are frequent.
|Exchange frequency increased by addition of Y or y<up>+</up>YL, but
|tetrad distribution remains abnormal.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000091	CLA 1 Aberration	GSYM 1 C(1)RR94-2F	DT 1 16 Jun 98	RESZ 439	REF 2	
ABSY|C(1)RR94-2F
DT|16 Jun 98
ID|FBab0000091
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0017221
|Sandler
|1965
|-1
}

DIS|Rosenfeld, 1964.
MU|X ray
PRG|C(1)TR94
CCM|C(1)RR94-2F, +.+; two X chromosomes of normal sequence
|attached proximally to a single centromere and joined
|distally by a segment of heterochromatin.
PHP|Tetrad distribution more nearly normal than in C(1)RR2.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000092	CLA 1 Aberration	NAM 1 Compound (1) of Sturtevant	GSYM 1 C(1)SB	DT 1 12 Nov 00	RESZ 788	SK 1	REF 3	
ABSY|C(1)SB
DT|12 Nov 00
NAM|Compound (1) of Sturtevant
ID|FBab0000092
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0018681
|Sandler and Lindsley
|1967
|-1
REFM|FBrf0010801
|Novitski and Sandler
|1956
|-1
}

DIS|Sturtevant and Beadle.
MU|recombination
PRG|In(1)y<up>4</up>
|C(1)RM
COR|exchange between the uninverted portion of In(1)y<up>4</up> and C(1)RM in a triploid
CCM|C(1)SB, +.In(1)y<up>4</up>; In(1)y<up>4</up> and a normal sequence
|attached proximally to a single centromere.
|A reversed metacentric heterozygous for @In(1)y<up>4</up>@.
BIP|1B1;18A3--4 (from In(1)y<up>4</up>)
PHP|Meiotic behavior similar to that of a tandem metacentric. Crossing
|over within inversion generates single ring, R(1)y<up>4</up>.
SK|FBstBL-3935
|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] w[a] bb[-]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0000096	CLA 1 Aberration	GSYM 1 C(1)TA.sc<up>V1</up>	DT 1 22 Aug 04	RESZ 650	REF 2	
ABSY|C(1)TA.sc<up>V1</up>
DT|22 Aug 04
ID|FBab0000096
REF
{
REFM|FBrf0019613
|Merriam
|1968
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
}

MU|recombination
PRG|C(1)TA.YL
|T(1;4)B<up>S</up>, B<up>S</up>
|In(1LR)sc<up>V1</up>, car . sc<up>V1</up> y<up>+</up>
COR|Derived as a recombinant in the B - car region between
|C(1)TA.YL and the X<up>P</up>4<up>D</up> element of T(1;4)B<up>SL</up>In(1LR)sc<up>V1R</up>, B<up>S</up> car . sc<up>V1</up> y<up>+</up>
CCM|C(1)TA.sc<up>V1</up>, + - +., y - y.sc<up>V1</up> y<up>+</up>.
BIP|1B2--12;h33--h34 (from In(1LR)sc<up>V1</up>)
|16A1;16A7--B1;102F (from T(1;4)B<up>S</up>)
}
# EOR
ABSR
{
RETE|ID 1 FBab0000095	CLA 1 Aberration	GSYM 1 C(1)TA.YL	DT 1 11 Feb 97	RESZ 595	REF 2	
ABSY|C(1)TA.YL
DT|11 Feb 97
ID|FBab0000095
REF
{
REFM|FBrf0019613
|Merriam
|1968
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
}

MU|spontaneous
|recombination
PRG|X.YS, In(1)sc<up>8L</up>EN<up>R</up>, y<up>+</up> y
|X.YL, y cv v f car
COR|thought to result from an euchromatic exchange
|between the X.YL chromosome and the acentric ring formed by
|dyscentric exchange between the distal and proximal
|heterochromatin of the long arm of X.YS, In(1)sc<up>8L</up>EN<up>R</up>.
CCM|C(1)TA.YL + - +., y - y.KL; original line segregating
|for cv, v, f, and car.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000093	CLA 1 Aberration	NAM 1 Compound (1) Tandem Acrocentric	GSYM 1 C(1)TA1	DT 1 12 Nov 00	RESZ 626	REF 2	
ABSY|C(1)TA1
DT|12 Nov 00
SYN|TA
NAM|Compound (1) Tandem Acrocentric
ID|FBab0000093
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009543
|Novitski
|1954
|-1
}

DIS|Novitski.
MU|X ray
PRG|In(1)sc<up>4</up>
|C(1;YL)1
COR|exchange of the proximal heterochromatin of In(1)sc<up>4</up> and YS of YSX.YL
CCM|C(1)TA1, In(1)sc<up>4</up> - In(1)EN.YL, y sc<up>4</up> - y..
BIP|1B3;h26--h28 (from In(1)sc<up>4</up>)
PHP|Produces a single, centric, rod-X chromosome and either an
|acentric, ring-X or a tandem triple-X chromosome by
|recombination between the proximal and distal X chromosomes.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000094	CLA 1 Aberration	GSYM 1 C(1)TA2	DT 1 04 Nov 98	RESZ 496	REF 2	
ABSY|C(1)TA2
DT|04 Nov 98
ID|FBab0000094
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0015576
|Sandler and Lindsley
|1963
|-1
}

DIS|Sandler and Lindsley.
MU|X ray
|recombination
PRG|YSX, y<up>+</up> YS . y cv v f
|XYL, y car . YL
COR|origin requires triple exchange.
CCM|C(1)TA2, + - +.; originally y cv f - y f..
AMD|bb \?
PHP|Generates single X chromosomes like C(1)TA1. Tetrad
|distribution about normal.
|C(1)TA2/0 lethal
}
# EOR
ABSR
{
RETE|ID 1 FBab0000097	CLA 1 Aberration	NAM 1 Compound (1) Tandem Metacentric of Hinton	GSYM 1 C(1)TM-H	DT 1 12 Nov 00	RESZ 834	REF 2	
ABSY|C(1)TM-H
DT|12 Nov 00
NAM|Compound (1) Tandem Metacentric of Hinton
ID|FBab0000097
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0011387
|Hinton
|1957
|-1
}

MU|recombination
PRG|Dp(1;1)B<up>S</up>-H
|In(1)dl-49
COR|Generated by exchange between the B<up>S</up> duplication and In(1)dl-49
CCM|C(1)TM-H, In(1)sc<up>4L</up>R(1)2<up>R</up> [.In(1)w<up>vC</up>]+dl-49;
|position of centromere indeterminate.
|Linear derivative of the unstable @R(1)2@, @In(1)w<up>vC</up>@.
BIP|4D7--E1;11F2--4 (from In(1)dl-49)
PHP|Exhibits variable stability as indicated by
|(a) their reduced recovery among the progeny of C(1)TM-H
|mothers, (b) the production of X0 patroclinous sons
|and (c) the instability of single rings produced by single
|exchange between the arms of the tandem metacentric.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000098	CLA 1 Aberration	NAM 1 Compound (1) Tandem Metacentric	GSYM 1 C(1)TM1	DT 1 22 Aug 04	RESZ 1022	REF 4	
ABSY|C(1)TM1
DT|22 Aug 04
NAM|Compound (1) Tandem Metacentric
ID|FBab0000098
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0008188
|Novitski
|1951
|-1
REFM|FBrf0007714
|Novitski and Lindsley
|1950
|-1
REFM|FBrf0010801
|Novitski and Sandler
|1956
|-1
}

DIS|Novitski, 1950.
MU|spontaneous
|recombination
PRG|R(1)2
|In(1)EN
COR|Product of one crossover between + and R(1)2 and one between In(1)EN and R(1)2 in a +/R(1)2/In(1)EN triploid
CCM|C(1)TM1, +.In(1)sc<up>8L</up>EN<up>R</up>, y Hw f . y<up>+</up> y f; a normal
|sequence and In(1)EN attached proximally to a single
|centromere derived from R(1)2.
BIP|1A;20F;20F (from In(1)EN)
|1A3--4;19F1--20A1 (from R(1)2)
PHP|Single crossover between the arms produces single-ring-X
|chromosome with the same structure as R(1)2 and an
|acentric-rod X chromosome. Tetrad distribution about normal
|(Novitski, 1951, Genetics 36: 267-80; Novitski and Sandler,
|1956, Genetics 41: 194-206.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000099	CLA 1 Aberration	GSYM 1 C(1)TM2	DT 1 04 Nov 98	RESZ 826	REF 2	
ABSY|C(1)TM2
DT|04 Nov 98
SYN|TMX y
ID|FBab0000099
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0017013
|Lindsley and Sandler
|1965
|-1
}

DIS|Lindsley and Sandler, 1963.
MU|X ray
PRG|X.YL, In(1)sc<up>4L</up>EN<up>R</up>
COR|exchange of the proximal heterochromatin of a normal X and YL of X.YL, In(1)sc<up>4L</up>EN<up>R</up>
CCM|C(1)TM2, +.In(1)sc<up>4L</up>EN<up>R</up>; originally y cv v sd . y sn g.
|The sequence in mitotic prophase is: the normal X
|euchromatin, two large heterochromatic segments, a small
|segment, the centromere, a small segment, the inverted X
|euchromatin.
PHP|Recombination between the arms produces a single-ring-X
|chromosome and an acentric, rod-X chromosome. Meiotic
|behavior similar to that of C(1)TM1; tetrad distribution
|about normal.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000100	CLA 1 Aberration	GSYM 1 C(1)TM5	DT 1 04 Nov 98	RESZ 817	REF 4	
ABSY|C(1)TM5
DT|04 Nov 98
ID|FBab0000100
REF
{
REFM|FBrf0016827
|Lucchesi et al.
|1965
|-1
REFM|FBrf0022726
|Pasztor
|1971
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0018407
|Pasztor
|1967
|-1
}

DIS|Lucchesi, Mills and Rosenbleeth.
MU|X ray
PRG|YSX.YL, In(1)EN, y w v f B
|XYL.YS, y . y<up>+</up>
CCM|C(1)TM5, YSIn(1)EN.+; originally y w v B KS . y
PHP|Single exchange generates highly unstable single ring
|chromosomes as seen by very low recovery of ring-bearing
|daughters and by 16-46% gynandromorphs among
|single-ring-bearing progeny. Single rings apparently
|deficient for proximal euchromatic material, as they are
|Male lethal in combination with a normal Y but survive in
|combination with B<up>S</up>Y or su(f)<up>+</up>Y.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000101	CLA 1 Aberration	NAM 1 Compound (1) Tandem	GSYM 1 C(1)TMB<up>S</up>9-1	DT 1 12 Nov 00	RESZ 1157	REF 2	
ABSY|C(1)TMB<up>S</up>9-1
DT|12 Nov 00
SYN|Dp(1;1)B<up>S</up>TRG
|TMXB<up>S</up>9-1
NAM|Compound (1) Tandem
ID|FBab0000101
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0017013
|Lindsley and Sandler
|1965
|-1
}

DIS|Lindsley and Sandler, 1963.
MU|X ray
PRG|Dp(1;1)B<up>S</up>TAG
|X.YL, In(1)sc<up>8L</up>EN<up>R</up>
COR|exchange of the proximal heterochromatin of Dp(1;1)B<up>S</up>TAG and YL of X.YL, In(1)sc<up>8L</up>EN<up>R</up>
CCM|C(1)TMB<up>S</up>9-1, Dp(1;1)B<up>S</up>TAG.In(1)sc<up>8L</up> EN<up>R</up>; originally
|B<up>S</up> y cv v sd . y sn g. The sequence in mitotic prophase is:
|the normal X euchromatin, two large heterochromatic
|segments, a small segment, the centromere, a small segment,
|the inverted X euchromatin.
BIP|15F9--16A1;20 (from Dp(1;1)B<up>S</up>TAG)
PHP|Recombination between the arms produces a single-ring-X
|chromosome, R(1)9-1 and an acentric, rod-X chromosome.
|Recombination between the B<up>S</up> duplication and the
|homologous region of the inverted arm generates a
|nontransmissible tandem-ring chromosome. Meiotic behavior
|similar to that of C(1)TM2.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000102	CLA 1 Aberration	GSYM 1 C(1)TMB<up>S</up>9-4	DT 1 12 Nov 00	RESZ 1092	REF 3	
ABSY|C(1)TMB<up>S</up>9-4
DT|12 Nov 00
SYN|Dp(1;1)B<up>S</up>TRG
|TMXB<up>S</up>9-4
ID|FBab0000102
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0128883
|Agudo et al.
|2000
|-1
REFM|FBrf0017013
|Lindsley and Sandler
|1965
|-1
}

DIS|Lindsley and Sandler, 1963.
MU|X ray
PRG|Dp(1;1)B<up>S</up>TAG
|X.YL, In(1)sc<up>8L</up>EN<up>R</up>
COR|exchange of the proximal heterochromatin (YL of X.YL)
CCM|C(1)TMB<up>S</up>9-4, Dp(1;1)B<up>S</up>TAG.In(1)sc<up>8L</up> EN<up>R</up>; originally
|B<up>S</up> y cv v sd . y sn g. The sequence in mitotic prophase is:
|the normal X euchromatin, a large heterochromatic segment, a
|small segment, the centromere, a small segment, the inverted
|X euchromatin.
BIP|15F9--16A1;20 (from Dp(1;1)B<up>S</up>TAG)
PHP|Recombination between arms produces single-ring-X
|chromosome, R(1)9-4 and an acentric, rod-X chromosome.
|Recombination between the B<up>S</up> duplication and the
|homologous region of the inverted arm produces a tandem-ring
|chromosome that may be transmissible.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000103	CLA 1 Aberration	NAM 1 Compound (1) Tandem Ring	GSYM 1 C(1)TR1	DT 1 16 Jun 98	RESZ 837	REF 2	
ABSY|C(1)TR1
DT|16 Jun 98
NAM|Compound (1) Tandem Ring
ID|FBab0000103
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0009543
|Novitski
|1954
|-1
}

DIS|Novitski.
MU|spontaneous
|recombination
PRG|C(1)TA1
CCM|C(1)TR1, In(1)sc<up>4</up> - In(1)EN., y<up>-</up> sc<up>-</up> - y..
OTH|the YL second arm had been replaced by the X<up>P</up>4<up>D</up> element of T(1;4)B<up>S</up> =
|T(1;4)15F9-16A1;16A7-B1;102F. A product of recombination
|between the duplicated B<up>S</up> second arm and the homologous
|region of the distal element of the tandem acrocentric.
PHP|Seems to be poorly transmissible (Novitski, 1954). Produces
|a centric, single-ring-X and either an acentric,
|single-ring-X or a tandem, triple-ring-X chromosome by
|recombination between the two elements of the compound.
}
# EOR
ABSR
{
RETE|ID 1 FBab0000104	CLA 1 Aberration	GSYM 1 C(1)TR94	DT 1 10 Aug 00	RESZ 1078	REF 4	
ABSY|C(1)TR94
DT|10 Aug 00
ID|FBab0000104
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0128883
|Agudo et al.
|2000
|-1
REFM|FBrf0018681
|Sandler and Lindsley
|1967
|-1
REFM|FBrf0033172
|Gatti et al.
|1979
|-1
}

DIS|Sandler and Lindsley.
MU|recombination
PRG|C(1)TMB<up>S</up>9-4
COR|Regular but infrequent product formed by
|exchange between the duplicated B<up>S</up> section and the
|homologous region of the inverted arm.
CCM|C(1)TR94, +.In(1)sc<up>4L</up>EN<up>R</up>.
OTH|Originally @y<up>1</up>@ @cv<up>1</up>@ @v<up>1</up>@
|@sd<up>1</up>@.@y<up>1</up>@ @sn<up>1</up>@ @g<up>1</up>@.
PHP|Produces a centric, single-ring-X and either an acentric,
|single-ring-X or a tandem, triple-ring-X chromosome by
|crossing over between the two arms of the compound.
|Transmission higher than that of C(1)TR1. Tetrad
|distribution about normal. Exhibits < 0.20% dicentric
|quadruple rings in mitotic metaphases (Gatti, Santini,
|Pimpinelli and Olivieri, 1979, Genetics 91: 255-74).
}
# EOR
ABSR
{
RETE|ID 1 FBab0000105	CLA 1 Aberration	NAM 1 Compound (1) of Valencia and Muller	GSYM 1 C(1)VM	DT 1 03 Jun 01	RESZ 1093	REF 2	
ABSY|C(1)VM
DT|03 Jun 01
NAM|Compound (1) of Valencia and Muller
ID|FBab0000105
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0007401
|Valencia et al.
|1949
|-1
}

DIS|Valencia, Muller and Valencia.
MU|X ray
PRG|In(1)sc<up>S1</up> + In(1)dl-49
COR|regularly X ray induced
|either by exchange between the proximal heterochromatin of the
|normal sequence and the distal heterochromatin of
|In(1)sc<up>S1</up> or by sister-strand union in one of the
|heterochromatic elements accompanied by normal euchromatic
|exchange.
CCM|Essentially a reversed acrocentric in which the proximal
|element contains @In(1)dl-49@.
|C(1)VM, + - In(1)sc<up>S1</up> In(1)dl-49.
OTH|Originally @y<up>1</up>@ @ac<up>1</up>@ @sc<up>1</up>@
|@pn<up>1</up>@ @w<up>1</up>@ @rb<up>1</up>@ @cm<up>1</up>@
|@ct<up>6</up>@ @sn<up>3</up>@ @oc<up>1</up>@ @ras<up>2</up>@ @v<up>1</up>@ @dy<up>1</up>@
|@g<up>1</up>@ @f<up>1</up>@ @car<up>1</up>@ -
|@y<up>1</up>@ @sc<up>S1</up>@ @lz<up>s</up>@ @B@.
PHP|Detachment by crossing over
|with a Y chromosome relatively frequent.
}
# EOR
ABSR
{
RETE|ID 1 FBab0010395	CLA 1 Aberration	GSYM 1 C(1;1;Y)4	DT 1 10 Feb 98	RESZ 751	REF 3	
ABSY|C(1;1;Y)4
DT|10 Feb 98
SYN|Y<up>S</up>X.Y<up>L</up>
|YSXX.YL
ID|FBab0010395
REF
{
REFM|FBrf0095657
|Mason et al.
|1997
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|recombination
COR|Exchange in triploid females carrying C(1)RA, first replacing the
|centromere region of the proximal X with that of YSX.YL, In(1)EN and then
|the terminus of the distal X with that of YSX.
CCM|An X-Y combination carrying a C(1)RA; the distal X is YSX in
|normal sequence and the proximal X is an inverted sequence
|with YL attached as a second arm.
REFDSR
{
RDID|FBrf0095657
|Mason et al.
|1997
SYN|Y<up>S</up>X.Y<up>L</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0027873	CLA 1 Aberration	GSYM 1 C(1;1;YL)RA<up>.</up>YL	DT 1 28 Sep 98	RESZ 567	SK 1	REF 1	
ABSY|C(1;1;YL)RA<up>.</up>YL
DT|28 Sep 98
ID|FBab0027873
REF
{
REFM|FBrf0100324
|Bloomington Drosophila Stock Center
|1998.1.9
|-1
}

PRG|In(1)sc<up>8L</up>EN<up>R</up>
CCM|Centromere presumably from @C(1;Y)1@.
MK|y<up>1</up> y<up>+</up>
REFDSR
{
RDID|FBrf0100324
|Bloomington Drosophila Stock Center
|1998.1.9
PRG|In(1)sc<up>8L</up>EN<up>R</up>
CCM|Centromere presumably from @C(1;Y)1@.
MK|y<up>1</up> y<up>+</up>
OTH|@In(1)sc<up>8L</up>EN<up>R</up>@ carries @y<up>1</up>@, and YL carries @y@<up>+</up>.
}

SK|FBstBL-4487
|C(1;1;YL)RA[.]YL: In(1)sc[8L]EN[R], y[1]: y[+]/Dp(1;YL)sc[S1]/C(1;Y)1, y[1] B[1]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0027874	CLA 1 Aberration	GSYM 1 C(1;1;YS)RM<up>.</up>YS	DT 1 12 Mar 98	RESZ 380	SK 1	REF 1	
ABSY|C(1;1;YS)RM<up>.</up>YS
DT|12 Mar 98
ID|FBab0027874
REF
{
REFM|FBrf0100324
|Bloomington Drosophila Stock Center
|1998.1.9
|-1
}

PRG|C(1;Y)1
CCM|Probably YSIn(1)EN<up>.</up>In(1)ENYS.
REFDSR
{
RDID|FBrf0100324
|Bloomington Drosophila Stock Center
|1998.1.9
PRG|C(1;Y)1
CCM|Probably YSIn(1)EN<up>.</up>In(1)ENYS.
}

SK|FBstBL-4462
|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
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010396	CLA 1 Aberration	GSYM 1 C(1;Y)1	DT 1 22 Aug 04	RESZ 2542	SK 333	REF 11	
ABSY|C(1;Y)1
DT|22 Aug 04
SYN|Y<up>S</up>X.Y<up>L</up>,In(1)En
|YSX.YL,In(1)EN,y<up>+</up>
|YSX.YL, In(1)EN
|C(1;Y)
|YSX.YL, In(1)24<up>L</up>A2<up>R</up>
|YSX.YL, In(1)26
ID|FBab0010396
REF
{
REFM|FBrf0007701
|Lindsley and Novitski
|1950
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0054128
|Rasooly and Robbins
|1991
|-1
REFM|FBrf0128883
|Agudo et al.
|2000
|-1
REFM|FBrf0152012
|Dauwalder et al.
|2002
|-1
REFM|FBrf0026093
|Craymer
|1974
|-1
REFM|FBrf0109049
|Sass and Henikoff
|1999
|-1
REFM|FBrf0008126
|Novitski
|1951
|-1
REFM|FBrf0158808
|Manheim and McKim
|2003
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
REFM|FBrf0059084
|Sawamura and Yamamoto
|1993
|-1
}

DIS|Lindsley, 1949.
MU|recombination
PRG|YSX, In(1)sc<up>8L</up>EN<up>R</up>
|y<up>+</up>Y
COR|exchange between the proximal heterochromatin of YSX, In(1)sc<up>8L</up>EN<up>R</up> and y<up>+</up>Y
CCM|YSX.YL, @In(1)EN@, YS @y@ . YL @y@<up>+</up>.
AMDP|Zhr
OTH|A derivative with B<up>S</up> at the end
|of YL described by Craymer (1974, D. I. S. 51: 21); also exists
|with various combinations of sex-linked markers. Two
|X-ray-induced paracentric-inversion derivatives described by
|Novitski: In(1)24, a nearly complete inversion with one
|break in the normally proximal euchromatin and the other in
|the centric heterochromatin and In(1)26 with one break in
|10A and one break in heterochromatin, distal or proximal not
|specified (Novitski, 1951, D. I. S. 25: 122; Lindsley and
|Novitski, 1959, Genetics 44: 187-96).
|Exists without the @y@<up>+</up> marker at the end of the YL arm.
PHP|male viable
|male fertile
REFDSR
{
RDID|FBrf0054128
|Rasooly and Robbins
|1991
CCM|X chromosome inserted between the two arms of the Y.
SYN|Y<up>S</up>X.Y<up>L</up>,In(1)En
}

REFDSR
{
RDID|FBrf0059084
|Sawamura and Yamamoto
|1993
AMDP|Zhr
OTH|Fails to rescue hybrid females from a cross between D.melanogaster
|males and D.sechellia females.
SYN|YSX.YL,In(1)EN,y<up>+</up>
}

REFDSR
{
RDID|FBrf0109049
|Sass and Henikoff
|1999
SYN|YSX.YL, In(1)EN
}

REFDSR
{
RDID|FBrf0128883
|Agudo et al.
|2000
SYN|Y<up>S</up>X.Y<up>L</up>,In(1)En
}

REFDSR
{
RDID|FBrf0158808
|Manheim and McKim
|2003
SYN|C(1;Y)
}

SK|FBstBL-4487
|C(1;1;YL)RA[.]YL: In(1)sc[8L]EN[R], y[1]: y[+]/Dp(1;YL)sc[S1]/C(1;Y)1, y[1] B[1]
|FBstBL-4462
|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
|FBstBL-1139
|C(1)M3, y[2]/0; CyO/T(2;3)ap[Xa] & C(1;Y)1, y[1]: y[+]/0; CyO/T(2;3)ap[Xa], ap[Xa]
|FBstBL-3923
|C(1)RA, In(1)AB, y[1], In(1)sc[8], sc[8]/Dp(1;YL)sc[S1]/C(1;Y)1, y[1] B[1]
|FBstBL-4486
|C(1)RA, y[1]: In(1)sc[8], sc[8]/Dp(1;YL)y[+]YL/C(1;Y)1, y[1] B[1]
|FBstBL-4248
|C(1)RM, y[1] pn[1] v[1]/C(1;Y)1, y[1] B[1]/0; sv[spa-pol]
|FBstBL-4485
|C(1)RM, y[1] sc[1] t[2] v[1] f[1] car[1]/C(1;Y)1, y[1] y[+] w[1] sn[5] oc[1] ptg[1] v[1]/0
|FBstBL-1612
|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
|FBstBL-3807
|C(1)RM, y[2] su(w[a])[1] w[a] 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]
|FBstBL-3219
|C(1;Y)1, Df(1)g, y[1] f[1] B[1]/C(1)A, y[1]/Dp(1;f)LJ9, y[+] g[+] na[+] Ste[+]
|FBstBL-705
|C(1;Y)1, In(1)dl-49, y[1]; bw[1]; e[4]; ci[1] ey[R]
|FBstBL-1394
|C(1;Y)1, In(1)dl-49, y[1] pn[62] v[Of] f[1]/0/C(1)M4
|FBstBL-1812
|C(1;Y)1, y[1]/0; Antp[Ns-rv11]/TM6
|FBstBL-4258
|C(1;Y)1, y[1]/0; bw[1]; e[4]; ci[1] ey[R]
|FBstBL-4408
|C(1;Y)1, y[1]/0; ry[506]
|FBstBL-4470
|C(1;Y)1, y[1]/0; st[1]
|FBstBL-2548
|C(1;Y)1, y[1] cv[1] B[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2549
|C(1;Y)1, y[1] cv[1] v[1] B[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2870
|C(1;Y)1, y[1] g[2] na[1]/FM3/Dp(1;f)LJ8, y[+] g[+] na[+] Ste[+]
|FBstBL-2962
|C(1;Y)1, y[1]; In(2L)Cy, In(2R)Cy/noc[Sco]
|FBstBL-1825
|C(1;Y)1, y[1]; In(3R)Antp[Ns-rv72], Antp[Ns-rv72] l(3)84Db[10]/TM6
|FBstBL-13435
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}CG11642[KG01407]; ry[506]
|FBstBL-13422
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}CG18823[KG01298]
|FBstBL-13407
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}CG9281[KG01147]; ry[506]
|FBstBL-13643
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG00095
|FBstBL-13383
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG00162/C(1)DX, y[1] f[1]; ry[506]
|FBstBL-13387
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG00217
|FBstBL-14884
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG01171
|FBstBL-13408
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG01177
|FBstBL-13409
|C(1;Y)1, y[1] P{y[+mDint2] w[BR.E.BR]=SUPor-P}KG01186; ry[506]
|total=
|333
SKC|333
}
# EOR
ABSR
{
RETE|ID 1 FBab0022015	CLA 1 Aberration	GSYM 1 C(1;Y)10	DT 1 29 Oct 99	RESZ 934	REF 3	
ABSY|C(1;Y)10
DT|29 Oct 99
SYN|Y<up>S</up>.X InEN B y.Y<up>L</up>
|YSX.YL,y,B
|YSX.YL,In(1)EN,Df(1)Zhr,y,B
|YSX.YL,In(1)EN,y,B
ID|FBab0022015
REF
{
REFM|FBrf0055832
|Hawley et al.
|1993
|-1
REFM|FBrf0031636
|Durica and Krider
|1978
|-1
REFM|FBrf0059084
|Sawamura and Yamamoto
|1993
|-1
}

PRG|C(1;Y)1
AMND|Zhr
REFDSR
{
RDID|FBrf0031636
|Durica and Krider
|1978
SYN|Y<up>S</up>.X InEN B y.Y<up>L</up>
}

REFDSR
{
RDID|FBrf0055832
|Hawley et al.
|1993
SYN|YSX.YL,y,B
}

REFDSR
{
RDID|FBrf0059084
|Sawamura and Yamamoto
|1993
PRG|C(1;Y)1
AMND|Zhr
PHP|Rescues hybrid females from a cross between D.melanogaster males and
|D.sechellia females.
OTH|Marker @y@<up>+</up> has been lost by an unknown rearrangement.
SYN|YSX.YL,In(1)EN,Df(1)Zhr,y,B
|YSX.YL,In(1)EN,y,B
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0010397	CLA 1 Aberration	GSYM 1 C(1;Y)108-9	DT 1 04 Nov 98	RESZ 575	SK 1	REF 3	
ABSY|C(1;Y)108-9
DT|04 Nov 98
SYN|XYL.YS108-9
ID|FBab0010397
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb
|y<up>+</up>Y
CCM|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) YL . YS.
PHP|male viable
|male fertile
SK|FBstBL-5952
|C(1;Y)108-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0022016	CLA 1 Aberration	GSYM 1 C(1;Y)11	DT 1 22 Aug 04	RESZ 459	REF 1	
ABSY|C(1;Y)11
DT|22 Aug 04
SYN|XYL.YS,y<up>2</up>,sc,cv,v,f
ID|FBab0022016
REF
{
REFM|FBrf0059084
|Sawamura and Yamamoto
|1993
|-1
}

PRG|C(1)RM
AMDP|Zhr
REFDSR
{
RDID|FBrf0059084
|Sawamura and Yamamoto
|1993
PRG|C(1)RM
AMDP|Zhr
OTH|Fails to rescue hybrid females from a cross between D.melanogaster
|males and D.sechellia females.
SYN|XYL.YS,y<up>2</up>,sc,cv,v,f
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0010398	CLA 1 Aberration	GSYM 1 C(1;Y)110-8	DT 1 12 Nov 00	RESZ 925	CLOC 1 h18--h25B	SK 1	REF 4	
ABSY|C(1;Y)110-8
DT|12 Nov 00
SYN|XYS.YL110-8
ID|FBab0010398
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0099369
|Lindsley
|1997.12.1
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

BPT|h18--h25B
DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb/y<up>+</up>Y
COR|Y breakpoint is distal to ks-2
CCM|All limits from polytene analysis (FBrf0099369)
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) YS . YL @y@<up>+</up>.
|YL may carry any marker available on the long arm
|of marked Y chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male viable
|male fertile
REFDSR
{
RDID|FBrf0099369
|Lindsley
|1997.12.1
BPT|h18--h25B
CCM|XYS.YL with the X in normal sequence. Possibly like @C(1;Y)8@.
}

SK|FBstBL-3758
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)110-8, y[2] y[+] su(w[a])[1] w[a]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010399	CLA 1 Aberration	GSYM 1 C(1;Y)112-17	DT 1 02 Jul 03	RESZ 750	CLOC 1 h1--h17;[]	SK 1	REF 4	
ABSY|C(1;Y)112-17
DT|02 Jul 03
SYN|XYL.YS112-17
ID|FBab0010399
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0099369
|Lindsley
|1997.12.1
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

BPT|h1--h17;[]
DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb
|y<up>+</up>Y
CCM|All limits from polytene analysis (FBrf0099369)
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) YL . YS.
PHP|male viable
|male fertile
REFDSR
{
RDID|FBrf0099369
|Lindsley
|1997.12.1
BPT|h1--h17
CCM|XYL.YS with the X in normal sequence. Like @C(1;Y)6@.
}

SK|FBstBL-4494
|C(1)RM, y[1] v[1] bb[-]/C(1;Y)112-17, y[2] su(w[a])[1] w[a]/0
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010400	CLA 1 Aberration	GSYM 1 C(1;Y)115-9	DT 1 12 Nov 00	RESZ 923	CLOC 1 h18--h25B	SK 1	REF 4	
ABSY|C(1;Y)115-9
DT|12 Nov 00
SYN|XYS.YL115-9
ID|FBab0010400
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0099369
|Lindsley
|1997.12.1
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

BPT|h18--h25B
DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb/y<up>+</up>Y
COR|Y breakpoint is distal to ks-2
CCM|All limits from polytene analysis (FBrf0099369)
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm
|of marked Y chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male viable
|male fertile
REFDSR
{
RDID|FBrf0099369
|Lindsley
|1997.12.1
BPT|h18--h25B
CCM|XYS.YL with the X in normal sequence. Possibly like @C(1;Y)8@.
}

SK|FBstBL-5953
|C(1;Y)115-9, y[2] su(w[a])[1] w[a]/C(1)RM, y[1] v[1] bb[1]/0
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0022017	CLA 1 Aberration	GSYM 1 C(1;Y)12	DT 1 08 Nov 97	RESZ 275	REF 1	
ABSY|C(1;Y)12
DT|08 Nov 97
SYN|YSX.YL,y,su(w<up>a</up>),w<up>a</up>
ID|FBab0022017
REF
{
REFM|FBrf0055832
|Hawley et al.
|1993
|-1
}

REFDSR
{
RDID|FBrf0055832
|Hawley et al.
|1993
SYN|YSX.YL,y,su(w<up>a</up>),w<up>a</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0010401	CLA 1 Aberration	GSYM 1 C(1;Y)129-11	DT 1 12 Nov 00	RESZ 745	CLOC 1 h1--h17	SK 1	REF 4	
ABSY|C(1;Y)129-11
DT|12 Nov 00
SYN|XYL.YS129-11
ID|FBab0010401
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0099369
|Lindsley
|1997.12.1
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

BPT|h1--h17
DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb
|y<up>+</up>Y
CCM|All limits from polytene analysis (FBrf0099369)
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male viable
|male fertile
REFDSR
{
RDID|FBrf0099369
|Lindsley
|1997.12.1
BPT|h1--h17
CCM|XYL.YS with the X in normal sequence. Like @C(1;Y)6@.
}

SK|FBstBL-4453
|C(1;Y)129-11, y[2] su(w[a])[1] w[a]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010402	CLA 1 Aberration	GSYM 1 C(1;Y)129-16	DT 1 20 Apr 00	RESZ 1178	SK 1	REF 5	
ABSY|C(1;Y)129-16
DT|20 Apr 00
SYN|XYL.YS129-16
ID|FBab0010402
REF
{
REFM|FBrf0019328
|Parker
|1968
|-1
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0111950
|Lilly and Botas
|1999
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0098436
|Wickline and Lindsley
|1997
|-1
}

DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb/y<up>+</up>Y
CCM|The break in the y<up>+</up>Y occurs between l(1)1Ac<up>+</up> and y<up>+</up> (Parker, 1968).
|Essentially an intact Y chromosome with all of the X
|euchromatin attached to YL distal to @y@<up>+</up>.
|Interstitial position of @y@<up>+</up> shown by recovery of @y@<up>+</up>
|reattachment.
|XYL.YS.
PED|position-effect variegation for: y
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) @y@<up>+</up> KL.KS.
PHP|interstitial y<up>+</up> allele shows strong variegation.
|male viable
|male fertile
REFDSR
{
RDID|FBrf0098436
|Wickline and Lindsley
|1997
SYN|C(1;Y)XYL<up>*</up>YS129-16
}

REFDSR
{
RDID|FBrf0111950
|Lilly and Botas
|1999
SYN|XYL-YS 129-16
}

SK|FBstBL-3752
|C(1)RM, y[1] v[1] bb[-]/0/C(1;Y)129-16, y[2] y[+] su(w[a])[1] w[a]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0023386	CLA 1 Aberration	GSYM 1 C(1;Y)13	DT 1 28 Jan 02	RESZ 194	SK 1	REF 1	
ABSY|C(1;Y)13
DT|28 Jan 02
ID|FBab0023386
REF
{
REFM|FBrf0141259
|Bloomington Drosophila Stock Center
|
|-1
}

DIS|M.M. Green.
MK|v<up>1</up> f<up>1</up>
OTH|structure not known
SK|FBstBL-16
|C(1)RM, y[1] P{w[+mC]=lacW}5-45fD w[*] P{lacW}4-5fP P{lacW}3-52d P{lacW}3-76a/0/C(1;Y)13, v[1] f[1]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010403	CLA 1 Aberration	GSYM 1 C(1;Y)2	DT 1 16 Jun 98	RESZ 417	SK 11	REF 2	
ABSY|C(1;Y)2
DT|16 Jun 98
SYN|YSX.YL
ID|FBab0010403
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Lindsley and Novitski.
MU|recombination
PRG|YSX
|C(1;YL)1
CCM|An attached XY with the X in normal sequence.
|YSX.YL, KS y.YL.
OTH|Commonly kept in stock as YSX.YL/0 males crossed to C(1)/0 females.
PHP|male viable
|male fertile
SK|FBstBL-2454
|C(1;Y)2, B[S], y[1] ct[6] f[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2501
|C(1;Y)2, B[S], y[1] v[1] bb[-]/0 & C(1)RM, y[1] v[1] bb[-]
|FBstBL-2486
|C(1;Y)2, y[+]/0 & C(1)RM, y[1] v[1]/0
|FBstBL-2498
|C(1;Y)2, y[1]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2510
|C(1;Y)2, y[1] B[1]/0 & C(1)RM, ras[l1]/0
|FBstBL-2487
|C(1;Y)2, y[1] B[1]/0 & C(1)RM, y[1] v[1]/0
|FBstBL-1608
|C(1;Y)2, y[1] ct[6] f[1] & C(1)DX, y[1] f[1]
|FBstBL-2545
|C(1;Y)2, y[1] f[1] B[S]/0 & C(1)RM, y[1] v[1] bb[-]/0
|FBstBL-2503
|C(1;Y)2, y[1] f[1] car[1]/0 & C(1)RM, y[1] v[1] bb[1]/0
|FBstBL-3710
|C(1;Y)2, y[1] P{w[+mC]=lacW}5-45fD w[*] P{w[+mC]=lacW}4-5fP P{w[+mC]=lacW}3-52d P{w[+mC]=lacW}3-76a: y[+]/0/C(1)RM, y[1] pn[1]
|FBstBL-1992
|Df(3R)A/Dp(3;3)Tpl; C(1)M3, y[2] bb[*]/C(1;Y)2, y[1]
SKC|11
}
# EOR
ABSR
{
RETE|ID 1 FBab0010404	CLA 1 Aberration	GSYM 1 C(1;Y)2-10T13	DT 1 16 Jun 98	RESZ 577	REF 3	
ABSY|C(1;Y)2-10T13
DT|16 Jun 98
SYN|XYL.YS2-10T13
ID|FBab0010404
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb
|y<up>+</up>Y
CCM|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male viable
|male fertile
}
# EOR
ABSR
{
RETE|ID 1 FBab0010405	CLA 1 Aberration	GSYM 1 C(1;Y)2-10T15	DT 1 16 Jun 98	RESZ 577	REF 3	
ABSY|C(1;Y)2-10T15
DT|16 Jun 98
SYN|XYL.YS2-10T15
ID|FBab0010405
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
MU|X ray
|detachment
PRG|C(1)RM, y<up>2</up> su(w<up>a</up>) bb
|y<up>+</up>Y
CCM|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male viable
|male fertile
}
# EOR
ABSR
{
RETE|ID 1 FBab0010406	CLA 1 Aberration	GSYM 1 C(1;Y)3	DT 1 16 Jun 98	RESZ 843	SK 1	REF 3	
ABSY|C(1;Y)3
DT|16 Jun 98
SYN|FM7Y
|YSX.YL, In(1)FM7
ID|FBab0010406
REF
{
REFM|FBrf0030180
|Mitchell
|1977
|-1
REFM|FBrf0026093
|Craymer
|1974
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
}

DIS|Craymer, April 1974.
MU|recombination
PRG|YSX, In(1)FM7, y<up>+</up> KS y<up>-</up> w<up>a</up> v<up>Of</up>
|YSX.YL, In(1)EN, KS y.KL B<up>S</up>
CCM|YSX.YL, In(1)FM7<up>L</up>EN<up>R</up>, y<up>+</up> KS y v<up>Of</up>.KL B<up>S</up>.
MK|y<up>+</up> y<up>1</up> v<up>Of</up> B<up>S</up>
OTH|such that the w<up>a</up> y<up>-</up>
|base of FM7 is replaced by the w<up>+</up> y.KL of YSX.YL,
|In(1)EN.
PHP|male viable
|male fertile
|The FM7
|inversions prevents euchromatic crossovers and the y<up>+</up> and
|B<up>S</up> markers serve to detect recombinational events in the
|heterochromatin.
SK|FBstBL-995
|C(1;Y)3, In(1)FM7, w[1] m[2]/0/C(1)M4, y[2]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0010407	CLA 1 Aberration	GSYM 1 C(1;Y)5	DT 1 16 Jun 98	RESZ 664	REF 4	
ABSY|C(1;Y)5
DT|16 Jun 98
SYN|YSXYL.
ID|FBab0010407
REF
{
REFM|FBrf0025061
|Donady et al.
|1973
|-1
REFM|FBrf0016239
|Novitski and Brosseau
|1964
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Lindsley.
MU|recombination
PRG|XYL.
|YSX
CCM|YSXYL., KS y<up>1</up> KL..
PHP|Shows extremely reduced recovery from above heterozygous
|females (Lindsley and Novitski, 1959), all zygotes carrying
|YSXYL. being lethal in some autosomal backgrounds;
|reciprocal recombinant recovered frequently (Novitski and
|Brosseau, 1964; Donady et al., 1973).
}
# EOR
ABSR
{
RETE|ID 1 FBab0022018	CLA 1 Aberration	GSYM 1 C(1;Y)6	DT 1 22 Aug 04	RESZ 486	SK 15	REF 3	
ABSY|C(1;Y)6
DT|22 Aug 04
SYN|XY<up>L</up>.Y<up>S</up>
|XYL.YS
ID|FBab0022018
REF
{
REFM|FBrf0174695
|Hirai et al.
|2004
|-1
REFM|FBrf0011879
|Brosseau and Lindsley
|1958
|-1
REFM|FBrf0086963
|Chubykin
|1996
|-1
}

CCM|XYL.YS
REFDSR
{
RDID|FBrf0011879
|Brosseau and Lindsley
|1958
SYN|XY<up>L</up>.Y<up>S</up>
}

REFDSR
{
RDID|FBrf0086963
|Chubykin
|1996
SYN|XY<up>L</up>.Y<up>S</up>
}

SK|FBstBL-1999
|C(1)M4, y[2]/C(1;Y)6, w[1118]
|FBstBL-2000
|C(1)M4, y[2]/Y & C(1;Y)6, w[1118]/Y
|FBstBL-3220
|C(1)RA, In(1)sc[J1], In(1)sc[8], l(1)1Ac[1], sc[J1] sc[8]/C(1;Y)6, Df(1)259, w[1]/Dp(1;Y)y[53i], y[53i] sc[8]
|FBstBL-1398
|C(1;Y)6, Dp(3;1)P115, y[2] sc[1] su(s)[2] pn[1] sn[3], y[+]/0 & C(1)M4, y[1]
|FBstBL-4555
|C(1;Y)6, y[1] fs(1)Yb[M104-2] cv[1] v[1]/FM7c
|FBstBL-5459
|C(1;Y)6, y[1] w[*] P{w[+*]=white-un4}BE1305 mew[023]/C(1)RM, y[1] pn[1] v[1]; Dp(1;f)y[+]
|FBstBL-1310
|C(1;Y)6, y[2] su(w[a])[1] w[a]/0/C(1)M4, y[1]
|FBstBL-1057
|Df(1)259, C(1;Y)6, w[1]/C(1)RM, y[1] v[1] f[1]; Dp(1;4)174/+
|FBstBL-3925
|Dp(1;f)1173; C(1)RA, Df(1)259, y[1]/C(1;Y)6, Df(1)259, y[1] w[1]
|FBstBL-3929
|Dp(1;f)122; C(1)RM, y[1] v[1] f[1]/C(1;Y)6, Df(1)259, w[1]
|FBstBL-3930
|Dp(1;f)164; C(1)RM, y[1] v[1]/C(1;Y)6, Df(1)259, w[1]
|FBstBL-3928
|Dp(1;f)18; C(1)RM, y[1] pn[1] v[1]/C(1;Y)6, Df(1)259, w[1]
|FBstBL-3926
|Dp(1;f)3; C(1)RM, y[1]/C(1;Y)6, Df(1)259, w[1]
|FBstBL-3806
|Dp(1;f)52; C(1)DX, y[1] f[1]/C(1;Y)6, Df(1)259, w[1]
|FBstBL-4060
|In(1)sc[8L]R(1)2[R], Dp(1;1)B[S]TMG, f[1] B[S]; T(1;4)B[S], C(1;Y)6, B[S]
SKC|15
}
# EOR
ABSR
{
RETE|ID 1 FBab0010408	CLA 1 Aberration	GSYM 1 C(1;Y)7	DT 1 16 Jun 98	RESZ 928	SK 1	REF 2	
ABSY|C(1;Y)7
DT|16 Jun 98
SYN|X-Y<up>bb-</up>
|XYL.YS, bb<up>-</up>
ID|FBab0010408
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0044481
|Komma and Endow
|1986
|-1
}

DIS|Komma.
MU|detachment
PRG|C(1)DX
|Dp(1;Ybb<up>-</up>)B<up>S</up>
COR|derived by detachment of the
|distal [In(1)dl-49] X of C(1)DX and its attachment to YL of
|B<up>S</up>Ybb<up>-</up> with loss of B<up>S</up>; In(1)dl-49 replaced by
|recombination.
CCM|A Ybb<up>-</up> chromosome with the X euchromatin attached (in
|normal sequence) distal to YL.
|XYL.YS, y<up>1</up> v<up>1</up> bb<up>-</up> KL.bb<up>-</up> KS.
AMD|bb
MK|y<up>1</up> v<up>1</up>
OTH|bb/XYL.YS, bb<up>-</up> females show an increase in the number of
|18S + 28S ribosomal genes (magnification) in their
|offspring.
|rDNA-deficient chromosome carrying most of B<up>S</up> Ybb<up>-</up>
PHP|male viable
|male fertile
SK|FBstBL-82
|C(1;Y)7, y[1] v[1] bb[-]: bb[-]/Dp(1;f)1185/C(1)DX, y[1] w[a]
SKC|1
}
# EOR
ABSR
{
RETE|ID 1 FBab0022019	CLA 1 Aberration	GSYM 1 C(1;Y)8	DT 1 28 Jan 02	RESZ 148	SK 4	REF 1	
ABSY|C(1;Y)8
DT|28 Jan 02
SYN|XYS.YL
ID|FBab0022019
REF
{
REFM|FBrf0141259
|Bloomington Drosophila Stock Center
|
|-1
}

CCM|XYS.YL
SK|FBstBL-1396
|C(1;Y)8, Dp(3;1)P115, y[1] pn[1] sn[3], B[S]/0/C(1)M4
|FBstBL-1397
|FBstBL-1397
|FBstBL-1395
|C(1;Y)8, Dp(3;1)P115, y[2] sc[1] su(s)[2] pn[1] sn[3]/0/C(1)M4, y[1]
|FBstBL-2496
|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]
SKC|4
}
# EOR
ABSR
{
RETE|ID 1 FBab0010409	CLA 1 Aberration	GSYM 1 C(1;Y)9	DT 1 10 Feb 98	RESZ 535	REF 3	
ABSY|C(1;Y)9
DT|10 Feb 98
SYN|X.YSYL
ID|FBab0010409
REF
{
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0019332
|Johnsen
|1968
|-1
REFM|FBrf0023023
|Johnsen and Zarrow
|1971
|-1
}

MU|X ray
PRG|X.YS, y w
|y<up>+</up>YL
CCM|X.Y, YL, y<up>1</up> w<up>1</up>.KS KL y<up>+</up>; metacentric chromosome.
PHP|Attached XY with X in normal sequence on one side of the
|centromere and a complete Y on the other.
|X.YSYL/0 males fertile
|transmission of the XY somewhat reduced.
}
# EOR
ABSR
{
RETE|ID 1 FBab0029161	CLA 1 Aberration	GSYM 1 C(1;Y)B<up>S</up>	DT 1 30 May 00	RESZ 306	REF 1	
ABSY|C(1;Y)B<up>S</up>
DT|30 May 00
ID|FBab0029161
REF
{
REFM|FBrf0011879
|Brosseau and Lindsley
|1958
|-1
}

MU|recombination
PRG|Ts(1Lt;4Lt)B<up>S</up>
|C(1;Y)6
REFDSR
{
RDID|FBrf0011879
|Brosseau and Lindsley
|1958
MU|recombination
PRG|Ts(1Lt;4Lt)B<up>S</up>
|C(1;Y)6
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0010410	CLA 1 Aberration	GSYM 1 C(1;Y)E12	DT 1 16 Jun 98	RESZ 790	REF 4	
ABSY|C(1;Y)E12
DT|16 Jun 98
SYN|XYL.YSE12
ID|FBab0010410
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|Y-chromosome breakpoint distal to @kl-5@.
|XYL.Y.
AMDD|kl-5
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010411	CLA 1 Aberration	GSYM 1 C(1;Y)E17	DT 1 16 Jun 98	RESZ 753	REF 4	
ABSY|C(1;Y)E17
DT|16 Jun 98
SYN|XYL.YSE17
ID|FBab0010411
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
AM|Y-chromosome breakpoint distal to kl-5.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010412	CLA 1 Aberration	GSYM 1 C(1;Y)F6	DT 1 16 Jun 98	RESZ 753	REF 4	
ABSY|C(1;Y)F6
DT|16 Jun 98
SYN|XYL.YSF6
ID|FBab0010412
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Y-chromosome breakpoint distal to @kl-5@.
|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010413	CLA 1 Aberration	GSYM 1 C(1;Y)G7	DT 1 10 Feb 98	RESZ 825	REF 4	
ABSY|C(1;Y)G7
DT|10 Feb 98
SYN|XYS.YLG7
ID|FBab0010413
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010414	CLA 1 Aberration	GSYM 1 C(1;Y)K1	DT 1 16 Jun 98	RESZ 753	REF 4	
ABSY|C(1;Y)K1
DT|16 Jun 98
SYN|XYL.YSK1
ID|FBab0010414
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Y-chromosome breakpoint distal to @kl-5@.
|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010415	CLA 1 Aberration	GSYM 1 C(1;Y)N10	DT 1 10 Feb 98	RESZ 827	REF 4	
ABSY|C(1;Y)N10
DT|10 Feb 98
SYN|XYS.YLN10
ID|FBab0010415
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010416	CLA 1 Aberration	GSYM 1 C(1;Y)N16	DT 1 16 Jun 98	RESZ 755	REF 4	
ABSY|C(1;Y)N16
DT|16 Jun 98
SYN|XYL.YSN16
ID|FBab0010416
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Y-chromosome breakpoint distal to @kl-5@.
|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010417	CLA 1 Aberration	GSYM 1 C(1;Y)N30	DT 1 10 Feb 98	RESZ 827	REF 4	
ABSY|C(1;Y)N30
DT|10 Feb 98
SYN|XYS.YLN30
ID|FBab0010417
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010418	CLA 1 Aberration	GSYM 1 C(1;Y)P1	DT 1 10 Feb 98	RESZ 768	REF 4	
ABSY|C(1;Y)P1
DT|10 Feb 98
SYN|XYS.YLP1
ID|FBab0010418
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
PHP|of marked Y chromosomes, e.g., y<up>+</up>, B<up>S</up>, etc.
|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010419	CLA 1 Aberration	GSYM 1 C(1;Y)P9	DT 1 16 Jun 98	RESZ 753	REF 4	
ABSY|C(1;Y)P9
DT|16 Jun 98
SYN|XYL.YSP9
ID|FBab0010419
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Y-chromosome breakpoint distal to @kl-5@.
|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0029162	CLA 1 Aberration	GSYM 1 C(1;Y)sc<up>260-14</up>	DT 1 12 Nov 00	RESZ 456	REF 1	
ABSY|C(1;Y)sc<up>260-14</up>
DT|12 Nov 00
SYN|C(1;Y)6, In(1)sc<up>260-14</up>
ID|FBab0029162
REF
{
REFM|FBrf0125111
|Gornek et al.
|2000.2.4
|-1
}

BIP|1B2--3;11D3--8 (from In(1)sc<up>260-14</up>)
MU|recombination
PRG|C(1;Y)6
|In(1)sc<up>260-14</up>
REFDSR
{
RDID|FBrf0125111
|Gornek et al.
|2000.2.4
MU|recombination
PRG|C(1;Y)6
|In(1)sc<up>260-14</up>
SYN|C(1;Y)6, In(1)sc<up>260-14</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0028794	CLA 1 Translocation	GSYM 1 C(1;Y)sc<up>7</up>	DT 1 12 Nov 00	RESZ 379	CLOC 1 [];h1--h17	REF 1	
ABSY|C(1;Y)sc<up>7</up>
DT|12 Nov 00
SYN|T(1;Y)sc<up>7</up>
ID|FBab0028794
REF
{
REFM|FBrf0109188
|Florence
|1999.7.22
|-1
}

BIP|1B4;6D8 (from In(1)sc<up>7</up>)
BPT|[];h1--h17
ACLA|Translocation
PRG|In(1)sc<up>7</up>
REFDSR
{
RDID|FBrf0109188
|Florence
|1999.7.22
BPT|[];h1--h17
ACLA|Translocation
PRG|In(1)sc<up>7</up>
}

}
# EOR
ABSR
{
RETE|ID 1 FBab0010420	CLA 1 Aberration	GSYM 1 C(1;Y)V13	DT 1 16 Jun 98	RESZ 755	REF 4	
ABSY|C(1;Y)V13
DT|16 Jun 98
SYN|XYL.YSV13
ID|FBab0010420
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

DIS|Parker.
COR|This compound structure is a frequent
|product of X-Y translocation induced in X/Y sperm, at least
|when the Y is B<up>S</up>Yy<up>+</up> (Kennison, 1981).
CCM|Y-chromosome breakpoint distal to @kl-5@.
|Essentially an intact Y chromosome with all of the X
|euchromatin appended distally to KL.
|XYL.Y.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KL.KS.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010421	CLA 1 Aberration	GSYM 1 C(1;Y)V23	DT 1 10 Feb 98	RESZ 825	REF 4	
ABSY|C(1;Y)V23
DT|10 Feb 98
SYN|XYS.YLV23
ID|FBab0010421
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., y<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010422	CLA 1 Aberration	GSYM 1 C(1;Y)V25	DT 1 10 Feb 98	RESZ 827	REF 4	
ABSY|C(1;Y)V25
DT|10 Feb 98
SYN|XYS.YLV25
ID|FBab0010422
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010423	CLA 1 Aberration	GSYM 1 C(1;Y)V36	DT 1 10 Feb 98	RESZ 827	REF 4	
ABSY|C(1;Y)V36
DT|10 Feb 98
SYN|XYS.YLV36
ID|FBab0010423
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one distal to ks-2 in B<up>S</up>Yy+ (Kennison, 1981).
CCM|Essentially an intact @Dp(1;Y)y<up>+</up>@ chromosome with all of the X
|euchromatin appended distally to YS.
|XYS.YL.
OTH|Originally @y<up>2</up>@ @su(w<up>a</up>)<up>1</up>@ @w<up>a</up>@ (@bb@?) KS.KL @y@<up>+</up>.
|YL may carry any marker available on the long arm of marked Y
|chromosomes, e.g., @y@<up>+</up>, @B<up>S</up>@, etc.
PHP|male fertile
|male viable
}
# EOR
ABSR
{
RETE|ID 1 FBab0010424	CLA 1 Aberration	GSYM 1 C(1;Y)V4	DT 1 10 Feb 98	RESZ 825	REF 4	
ABSY|C(1;Y)V4
DT|10 Feb 98
SYN|XYS.YLV4
ID|FBab0010424
REF
{
REFM|FBrf0012016
|Parker and McCrone
|1958
|-1
REFM|FBrf0066905
|Lindsley and Zimm
|1992
|-1
REFM|FBrf0036525
|Kennison
|1981
|-1
REFM|FBrf0012642
|Lindsley and Novitski
|1959
|-1
}

MU|segregation
COR|from translocation with one break in X heterochromatin
|and one