ABSR
{
RETE|ID 1 PFab0900000	CLA 1 Aberration	GSYM 1 Df(1)LIMK1-3	DT 1 30 Oct 06	RESZ 230	REF 1	
ABSY|Df(1)LIMK1-3
DT|30 Oct 06
ID|PFab0900000
REF
{
REFM|FBrf0190083
|Ang et al.
|2006
|0
}

REFDSR
{
RDID|FBrf0190083
|Ang et al.
|2006
AM|Deletes LIMK1 (molecular determination)
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900001	CLA 1 Aberration	GSYM 1 Df(1)LIMK1-5	DT 1 30 Oct 06	RESZ 1210	REF 1	
ABSY|Df(1)LIMK1-5
DT|30 Oct 06
ID|PFab0900001
REF
{
REFM|FBrf0190083
|Ang et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190083
|Ang et al.
|2006
SYN|Limk<up>5</up>
AM|Deletes LIMK1 (molecular determination)
PHP|@Df(1)LIMK1-5@ mutants have slightly smaller muscle fibers than wild
|type and the mutant NMJs have an expanded morphology compared to wild
|type. The @Df(1)LIMK1-5@ NMJs exhibit increased bouton number (by
|73-112%). However, the function of @Df(1)LIMK1-5@ NMJs is normal,
|as judged by evoked Excitatory Potentials (mEJPs). @Df(1)LIMK1-5@
|NMJs have slightly fewer active zones per bouton than wild type, suggesting
|that it is this compensatory mechanism that makes the function normal.
|The patterns of axon trajectories in both the CNS and PNS are normal
|in @Df(1)LIMK1-5@ mutants. The differentiation of the olfactory receptors
|and the targeting of their axons is normal in these mutants.
|Expression of @Pak<up>Scer\UAS.T:Myr1</up>@ under the control of @Scer\GAL4<up>SG18.1</up>@
|in a @Df(1)LIMK1-5@ background suppresses the antennal lobe anatomy
|phenotype seen when this transgene is expressed in a wild type background.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000564	CLA 1 Aberration	GSYM 1 Df(1)N-54l9	DT 1 30 Oct 06	RESZ 450	REF 1	
ABSY|Df(1)N-54l9
DT|30 Oct 06
ID|PFab0000564
REF
{
REFM|FBrf0190031
|Maitra et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190031
|Maitra et al.
|2006
SYN|N<up>54l9</up>
AMD|N
PHP|@Df(1)N-54l9@ heterozygotes exhibit notches at the wing margin.
|@Df(1)N-54l9@ @Mer<up>4</up>@; @ex<up>e1</up>@ triple transheterozygous mutants suppress
|the @Df(1)N-54l9@ heterozygous wing notch phenotype.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000580	CLA 1 Aberration	GSYM 1 Df(1)N-81k1	DT 1 30 Oct 06	RESZ 218	REF 1	
ABSY|Df(1)N-81k1
DT|30 Oct 06
ID|PFab0000580
REF
{
REFM|FBrf0190133
|Koelzer and Klein
|2006
|-1
}

REFDSR
{
RDID|FBrf0190133
|Koelzer and Klein
|2006
SYN|Df(1)N<up>81k</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000668	CLA 1 Aberration	GSYM 1 Df(1)RF19	DT 1 30 Oct 06	RESZ 197	REF 1	
ABSY|Df(1)RF19
DT|30 Oct 06
ID|PFab0000668
REF
{
REFM|FBrf0190539
|Chen et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190539
|Chen et al.
|2006
SYN|Df(1)RF19
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000798	CLA 1 Aberration	GSYM 1 Df(1)ct4b1	DT 1 30 Oct 06	RESZ 199	REF 1	
ABSY|Df(1)ct4b1
DT|30 Oct 06
ID|PFab0000798
REF
{
REFM|FBrf0190539
|Chen et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190539
|Chen et al.
|2006
SYN|Df(1)ct4b1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900002	CLA 1 Aberration	GSYM 1 Df(1)moody-&Dgr;17	DT 1 30 Oct 06	RESZ 591	REF 1	
ABSY|Df(1)moody-&Dgr;17
DT|30 Oct 06
ID|PFab0900002
REF
{
REFM|FBrf0189897
|Bainton et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0189897
|Bainton et al.
|2005
AMD|moody
|CG4313
|CG4290
PHP|Only ~1% of homozygous females and hemizygous males survive to adulthood.
|These survivors show severe motor defects and have a reduced lifespan
|compared to wild-type flies. These flies show a breakdown of the blood-brain
|barrier, as assessed by the penetrance of a fluorescent dye into the
|retina.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900003	CLA 1 Aberration	GSYM 1 Df(1)moody-&Dgr;18	DT 1 30 Oct 06	RESZ 458	REF 1	
ABSY|Df(1)moody-&Dgr;18
DT|30 Oct 06
ID|PFab0900003
REF
{
REFM|FBrf0189897
|Bainton et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0189897
|Bainton et al.
|2005
AM|Deletes moody (molecular determination)
|Deletes CG4325 (molecular determination)
PHP|Only ~1% of homozygous females and hemizygous males survive to adulthood.
|These survivors show severe motor defects and have a reduced lifespan
|compared to wild-type flies.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000868	CLA 1 Aberration	GSYM 1 Df(1)os1A2	DT 1 30 Oct 06	RESZ 521	REF 1	
ABSY|Df(1)os1A2
DT|30 Oct 06
ID|PFab0000868
REF
{
REFM|FBrf0190126
|Hombria et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0190126
|Hombria et al.
|2005
SYN|Df(1)os<up>1A</up>
AM|Deletes os (molecular determination)
|Deletes upd2 (molecular determination)
|Deletes upd3 (molecular determination)
PHP|@Df(1)os1A2@ embryos show segmentation defects, with all segments affected.
|The posterior spiracles and trachea are missing from these embryos
|and the mandible is abnormal.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000867	CLA 1 Aberration	GSYM 1 Df(1)os<up>UE69</up>	DT 1 30 Oct 06	RESZ 288	REF 1	
ABSY|Df(1)os<up>UE69</up>
DT|30 Oct 06
ID|PFab0000867
REF
{
REFM|FBrf0190126
|Hombria et al.
|2005
|-1
}

ASAL|upd3<up>UE69</up>
AM|Deletes os (molecular determination)
|Deletes upd3 (molecular determination)
|Does not delete upd2 (molecular determination)
}
# EOR
ABSR
{
RETE|ID 1 PFab0900004	CLA 1 Aberration	GSYM 1 Df(2L)BSC142	DT 1 30 Oct 06	RESZ 281	REF 1	
ABSY|Df(2L)BSC142
DT|30 Oct 06
ID|PFab0900004
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC142
OAB|Inferred to overlap with: @Df(2L)BSC192@.
|Fails to complement @Df(2L)BSC192@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900005	CLA 1 Aberration	GSYM 1 Df(2L)BSC162	DT 1 30 Oct 06	RESZ 806	REF 1	
ABSY|Df(2L)BSC162
DT|30 Oct 06
ID|PFab0900005
REF
{
REFM|636516406
|Christensen
|20006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|636516406
|Christensen
|20006.8.29
SYN|Df(2L)BSC162
BPT|P{XP}v(2)k05816<up>d04154</up>;PBac{WH}CG3488<up>f05535</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of Df(2L)BSC162 predicted from the Release
|4 genomic coordinates of the @P{XP}v(2)k05816<up>d04154</up>@ and @PBac{WH}CG3488<up>f05535</up>@
|progenitor insertion sites are 23C5;23D4.
MU|FLPase
PRG|P{XP}v(2)k05816<up>d04154</up>
|PBac{WH}CG3488<up>f05535</up>
AMD|toc
|Mad
OTH|Presence of @P+PBac{XP5.WH5}BSC162@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC162
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900006	CLA 1 Aberration	GSYM 1 Df(2L)BSC163	DT 1 30 Oct 06	RESZ 781	REF 1	
ABSY|Df(2L)BSC163
DT|30 Oct 06
ID|PFab0900006
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC163
BPT|P{XP}v(2)k05816<up>d04154</up>;PBac{WH}CG9662<up>f06279</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC163@ predicted from the Release
|4 genomic coordinates of the progenitor @P{XP}v(2)k05816<up>d04154</up>@ and
|@PBac{WH}CG9662<up>f06279</up>@ insertion sites are 23C5;23F1.
MU|FLPase
PRG|P{XP}v(2)k05816<up>d04154</up>
|PBac{WH}CG9662<up>f06279</up>
AMD|toc
|Mad
OTH|Presence of @P+PBac{XP5.WH5}BSC163@ was verified using the PCR methods
|and primers described in FBrf0175003.
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900007	CLA 1 Aberration	GSYM 1 Df(2L)BSC167	DT 1 30 Oct 06	RESZ 728	REF 1	
ABSY|Df(2L)BSC167
DT|30 Oct 06
ID|PFab0900007
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC167
BPT|PBac{WH}CG31989<up>f02191</up>;P{XP}d04336
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC167@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{WH}CG31989<up>f02191</up>@ and
|@P{XP}d04336@ insertion sites are 25E5;25E6.
MU|FLPase
PRG|PBac{WH}CG31989<up>f02191</up>
|P{XP}d04336
AMD|CG7277
OTH|Presence of @P+PBac{XP5.WH5}BSC167@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC167
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900008	CLA 1 Aberration	GSYM 1 Df(2L)BSC168	DT 1 30 Oct 06	RESZ 821	REF 1	
ABSY|Df(2L)BSC168
DT|30 Oct 06
ID|PFab0900008
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC168
BPT|PBac{WH}CG11030<up>f07078</up>;P{XP}eIF-4a<up>d06487</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC168@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{WH}CG11030<up>f07078</up>@ and
|@P{XP}eIF-4a<up>d06487</up>@ insertion sites are 25F4;26B2.
MU|FLPase
PRG|PBac{WH}CG11030<up>f07078</up>
|P{XP}eIF-4a<up>d06487</up>
AMD|Vm26Ab
AMDP|Vm26Ab
|chic
OTH|Presence of @P+PBac{XP5.WH5}BSC168@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC168
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900009	CLA 1 Aberration	GSYM 1 Df(2L)BSC169	DT 1 30 Oct 06	RESZ 751	REF 1	
ABSY|Df(2L)BSC169
DT|30 Oct 06
ID|PFab0900009
REF
{
REFM|-1742681692
|Christensen
|2006.7.11
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742681692
|Christensen
|2006.7.11
SYN|Df(2L)BSC169
BPT|P{XP}CG6907<up>d06812</up>;PBac{WH}CG14007<up>f07713</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC169@ predicted from the transposable
|element insertions sites using Release 4 are 25E5;25F3.
MU|FLPase
PRG|P{XP}CG6907<up>d06812</up>
|PBac{WH}CG14007<up>f07713</up>
AMD|CG7277
|Hel25E
|Lam
OTH|Presence of @P+PBac{XP5.WH5}BSC169@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC169
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900010	CLA 1 Aberration	GSYM 1 Df(2L)BSC171	DT 1 30 Oct 06	RESZ 891	REF 1	
ABSY|Df(2L)BSC171
DT|30 Oct 06
ID|PFab0900010
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC171
BPT|PBac{RB}CG2818<up>e00947</up>;P{XP}d07508
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC171@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{RB}CG2818<up>e00947</up>@ and
|@P{XP}d07508@ insertion sites are 24C1;24C6.
MU|FLPase
PRG|PBac{RB}CG2818<up>e00947</up>
|P{XP}d07508
AMD|bowl
OTH|Presence of @P+PBac{XP5.RB3}BSC171@ was verified using the PCR methods
|and primers described in FBrf0175003 with the substitution of the primer
|5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer
|in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC171
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900011	CLA 1 Aberration	GSYM 1 Df(2L)BSC172	DT 1 30 Oct 06	RESZ 829	REF 1	
ABSY|Df(2L)BSC172
DT|30 Oct 06
ID|PFab0900011
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
BPT|P{XP}d01421;PBac{RB}e03037
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of Df(2L)BSC172 predicted from the Release
|4 genomic coordinates of the progenitor @P{XP}d01421@ and @PBac{RB}e03037@
|insertion sites are 25B10;25C1.
MU|FLPase
PRG|P{XP}d01421
|PBac{RB}e03037
AMD|vkg
OTH|Presence of @P+PBac{XP5.RB3}BSC172@ was verified using the PCR methods
|and primers described in FBrf0175003, with the substitution of the
|primer 5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus
|primer in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC172
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900012	CLA 1 Aberration	GSYM 1 Df(2L)BSC180	DT 1 30 Oct 06	RESZ 977	REF 1	
ABSY|Df(2L)BSC180
DT|30 Oct 06
ID|PFab0900012
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC180
BPT|PBac{RB}CG31694<up>e03952</up>;P{XP}d02451
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC180@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{RB}CG31694<up>e03952</up>@ and
|@P{XP}d02451@ insertion sites are 23B7;23C2.
MU|FLPase
PRG|PBac{RB}CG31694<up>e03952</up>
|P{XP}d02451
AMD|lilli
OAB|Fails to complement @Df(2L)ED206@.
|Inferred to overlap with: @Df(2L)ED206@.
OTH|Presence of @P+PBac{XP5.RB3}BSC180@ was verified using the PCR methods
|and primers described in FBrf0175003 with the substitution of the primer
|5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer
|in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC180
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900013	CLA 1 Aberration	GSYM 1 Df(2L)BSC183	DT 1 30 Oct 06	RESZ 935	REF 1	
ABSY|Df(2L)BSC183
DT|30 Oct 06
ID|PFab0900013
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC183
BPT|P{XP}CG9016<up>d08241</up>;PBac{RB}Ucp4C<up>e03988</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC183@ predicted from the Release
|4 genomic coordinates of the progenitor @P{XP}CG9016<up>d08241</up>@ and @PBac{RB}Ucp4C<up>e03988</up>@
|insertion sites are 26A1;26A5.
MU|FLPase
PRG|P{XP}CG9016<up>d08241</up>
|PBac{RB}Ucp4C<up>e03988</up>
AMD|Vm26Ab
OTH|Presence of @P+PBac{XP5.RB3}BSC183@ was verified using the PCR methods
|and primers described in FBrf0175003 with the substitution of the primer
|5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer
|in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC183
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900014	CLA 1 Aberration	GSYM 1 Df(2L)BSC184	DT 1 30 Oct 06	RESZ 752	REF 1	
ABSY|Df(2L)BSC184
DT|30 Oct 06
ID|PFab0900014
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC184
BPT|P{XP}d06368;PBac{WH}CG9135<up>f03307</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC184@ predicted from the Release
|4 genomic coordinates of the progenitor @P{XP}d06368@ and @PBac{WH}CG9135<up>f03307</up>@
|insertion sites are 26A8;26B5.
MU|FLPase
PRG|P{XP}d06368
|PBac{WH}CG9135<up>f03307</up>
AMD|eIF-4a
|ifc
OTH|Presence of @P+PBac{XP5.WH5}BSC184@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC184
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900015	CLA 1 Aberration	GSYM 1 Df(2L)BSC185	DT 1 30 Oct 06	RESZ 763	REF 1	
ABSY|Df(2L)BSC185
DT|30 Oct 06
ID|PFab0900015
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC185
BPT|PBac{WH}f01456;P{XP}d01131
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC185@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{WH}f01456@ and @P{XP}d01131@
|insertions are 26B10;26D7.
MU|FLPase
PRG|PBac{WH}f01456
|P{XP}d01131
AMD|Gef26
OAB|Inferred to overlap with: @Df(2L)Exel6016@.
|Fails to complement @Df(2L)Exel6016@.
OTH|Presence of @P+PBac{XP5.WH5}BSC185@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC185
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900016	CLA 1 Aberration	GSYM 1 Df(2L)BSC186	DT 1 30 Oct 06	RESZ 687	REF 1	
ABSY|Df(2L)BSC186
DT|30 Oct 06
ID|PFab0900016
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC186
BPT|P{XP}d06531;PBac{WH}f00173
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC186@ predicted from the Release
|4 genomic coordinates of the transposable element insertion sites are
|26C1;26C3.
MU|FLPase
PRG|P{XP}d06531
|PBac{WH}f00173
AMD|Gef26
OAB|Complements @Df(2L)Exel6016@.
OTH|Presence of @P+PBac{XP5.WH5}BSC186@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC186
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900017	CLA 1 Aberration	GSYM 1 Df(2L)BSC189	DT 1 30 Oct 06	RESZ 1033	REF 1	
ABSY|Df(2L)BSC189
DT|30 Oct 06
ID|PFab0900017
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC189
BPT|PBac{RB}CG5149<up>e03983</up>;P{XP}d04880
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC189@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{RB}CG5149<up>e03983</up>@ and
|@P{XP}d04880@ insertion sites are 27F3;28C4.
MU|FLPase
PRG|PBac{RB}CG5149<up>e03983</up>
|P{XP}d04880
OAB|Inferred to overlap with: @Df(2L)ED499@.
|Fails to complement @Df(2L)ED499@.
|Inferred to overlap with: @Df(2L)Exel7031@.
|Fails to complement @Df(2L)Exel7031@.
OTH|Presence of @P+PBac{XP5.RB3}BSC189@ was verified using the PCR methods
|and primers described in FBrf0175003 with the substitution of the primer
|5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer
|in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC189
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900018	CLA 1 Aberration	GSYM 1 Df(2L)BSC192	DT 1 30 Oct 06	RESZ 814	REF 1	
ABSY|Df(2L)BSC192
DT|30 Oct 06
ID|PFab0900018
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)BSC192
BPT|P{XP}TepIII<up>d03976</up>;PBac{WH}CG7221<up>f04545</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC192@ predicted from the Release
|4 genomic coordinates of the progenitor @P{XP}TepIII<up>d03976</up>@ and @PBac{WH}CG7221<up>f04545</up>@
|insertion sites are 28C1;28D3.
PRG|P{XP}TepIII<up>d03976</up>
|PBac{WH}CG7221<up>f04545</up>
OAB|Inferred to overlap with: @Df(2L)BSC142@.
|Fails to complement @Df(2L)BSC142@.
OTH|Presence of @P+PBac{XP5.WH5}BSC192@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC192
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900019	CLA 1 Aberration	GSYM 1 Df(2L)BSC202	DT 1 30 Oct 06	RESZ 836	REF 1	
ABSY|Df(2L)BSC202
DT|30 Oct 06
ID|PFab0900019
REF
{
REFM|-1742651840
|Christensen
|2006.8.30
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651840
|Christensen
|2006.8.30
SYN|Df(2L)BSC202
BPT|P{XP}d03596;PBac{RB}e00922
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC202@ predicted from the progenitor
|@P{XP}d03596@ and @PBac{RB}e00922@ insertion sites using Release 4
|coordinates are 29D5;29F3.
MU|FLPase
PRG|P{XP}d03596
|PBac{RB}e00922
AMD|raw
OTH|Presence of @P+PBac{XP5.RB3}BSC202@ was verified using the PCR methods
|and primers described in FBrf0175003 with the substitution of the primer
|5'-CCAATGCGTTTATTTCAGGTCACG-3' for the RB3' plus or RB3' minus primer
|in the Hybrid PCR protocol in the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC202
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900020	CLA 1 Aberration	GSYM 1 Df(2L)BSC211	DT 1 30 Oct 06	RESZ 718	REF 1	
ABSY|Df(2L)BSC211
DT|30 Oct 06
ID|PFab0900020
REF
{
REFM|-1742651840
|Christensen
|2006.8.30
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651840
|Christensen
|2006.8.30
SYN|Df(2L)BSC211
BPT|P{XP}d02789;PBac{WH}CG31871<up>f02763</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC211@ predicted from the progenitor
|@P{XP}d02789@ and @PBac{WH}CG31871<up>f02763</up>@ insertions sites using
|Release 4 coordinates are 31F4;32A3.
MU|FLPase
PRG|P{XP}d02789
|PBac{WH}CG31871<up>f02763</up>
AMD|Fatp
OTH|Presence of @P+PBac{XP5.WH5}BSC211@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC211
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900021	CLA 1 Aberration	GSYM 1 Df(2L)BSC213	DT 1 30 Oct 06	RESZ 742	REF 1	
ABSY|Df(2L)BSC213
DT|30 Oct 06
ID|PFab0900021
REF
{
REFM|-1742651840
|Christensen
|2006.8.30
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651840
|Christensen
|2006.8.30
SYN|Df(2L)BSC213
BPT|PBac{WH}Nos<up>f02469</up>;P{XP}aub<up>d04301</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC213@ predicted from the @PBac{WH}Nos<up>f02469</up>@
|and @P{XP}aub<up>d04301</up>@ progenitor insertions sites using Release 4
|coordinates are 32B1;32C1.
MU|FLPase
PRG|PBac{WH}Nos<up>f02469</up>
|P{XP}aub<up>d04301</up>
AMD|piwi
OTH|Presence of @P+PBac{XP5.WH5}BSC213@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC213
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900022	CLA 1 Aberration	GSYM 1 Df(2L)BSC216	DT 1 30 Oct 06	RESZ 765	REF 1	
ABSY|Df(2L)BSC216
DT|30 Oct 06
ID|PFab0900022
REF
{
REFM|-1742651840
|Christensen
|2006.8.30
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651840
|Christensen
|2006.8.30
SYN|Df(2L)BSC216
BPT|PBac{WH}Nckx30C<up>f04751</up>;P{XP}CG13124<up>d10773</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2L)BSC216@ predicted from the @PBac{WH}Nckx30C<up>f04751</up>@
|and @P{XP}CG13124<up>d10773</up>@ progenitor insertions sites using Release
|4 coordinates are 30C6;30E1.
MU|FLPase
PRG|PBac{WH}Nckx30C<up>f04751</up>
|P{XP}CG13124<up>d10773</up>
AMD|und
OTH|Presence of @P+PBac{XP5.WH5}BSC216@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC216
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0022184	CLA 1 Aberration	GSYM 1 Df(2L)C144	DT 1 30 Oct 06	RESZ 533	REF 1	
ABSY|Df(2L)C144
DT|30 Oct 06
ID|PFab0022184
REF
{
REFM|478531783
|McDaniel
|2006.10.11
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|478531783
|McDaniel
|2006.10.11
SYN|Df(2L)C144
|Df(2L)c144
CCM|PCR amplification of the @Chd1@ genomic region from flies carrying
|@Df(2L)C144@ over a large @Chd1@ deletion shows that the right limit
|of breakpoint 2 for @Df(2L)C144@ lies to the left of @Chd1@.
AMDD|Chd1
AM|Deletes Drp1 (molecular determination)
|Deletes l(2)23AB2 (molecular determination)
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0031922	CLA 1 Aberration	GSYM 1 Df(2L)ED206	DT 1 30 Oct 06	RESZ 279	REF 1	
ABSY|Df(2L)ED206
DT|30 Oct 06
ID|PFab0031922
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)ED206
OAB|Fails to complement @Df(2L)BSC180@.
|Inferred to overlap with: @Df(2L)BSC180@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0032212	CLA 1 Aberration	GSYM 1 Df(2L)ED499	DT 1 30 Oct 06	RESZ 279	REF 1	
ABSY|Df(2L)ED499
DT|30 Oct 06
ID|PFab0032212
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)ED499
OAB|Inferred to overlap with: @Df(2L)BSC189@.
|Fails to complement @Df(2L)BSC189@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0037858	CLA 1 Aberration	GSYM 1 Df(2L)Exel6016	DT 1 30 Oct 06	RESZ 458	REF 1	
ABSY|Df(2L)Exel6016
DT|30 Oct 06
ID|PFab0037858
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)Exel6016
OAB|Inferred to overlap with: @Df(2L)BSC185@.
|Fails to complement @Df(2L)Exel6016@.
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)Exel6016
OAB|Complements @Df(2L)BSC186@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0037903	CLA 1 Aberration	GSYM 1 Df(2L)Exel7021	DT 1 30 Oct 06	RESZ 155	REF 1	
ABSY|Df(2L)Exel7021
DT|30 Oct 06
ID|PFab0037903
REF
{
REFM|-556778046
|Koh
|2006
|-1
|Science 312: 1809--1812
}

REFDSR
{
RDID|-556778046
|Koh
|2006
SYN|Df(2L)Exel7021
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0037910	CLA 1 Aberration	GSYM 1 Df(2L)Exel7031	DT 1 30 Oct 06	RESZ 285	REF 1	
ABSY|Df(2L)Exel7031
DT|30 Oct 06
ID|PFab0037910
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2L)Exel7031
OAB|Inferred to overlap with: @Df(2L)BSC189@.
|Fails to complement @Df(2L)BSC189@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0037952	CLA 1 Aberration	GSYM 1 Df(2L)Exel8012	DT 1 30 Oct 06	RESZ 155	REF 1	
ABSY|Df(2L)Exel8012
DT|30 Oct 06
ID|PFab0037952
REF
{
REFM|-556778046
|Koh
|2006
|-1
|Science 312: 1809--1812
}

REFDSR
{
RDID|-556778046
|Koh
|2006
SYN|Df(2L)Exel8012
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001468	CLA 1 Aberration	GSYM 1 Df(2L)GpdhA	DT 1 30 Oct 06	RESZ 555	REF 1	
ABSY|Df(2L)GpdhA
DT|30 Oct 06
ID|PFab0001468
REF
{
REFM|FBrf0190096
|Buescher et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190096
|Buescher et al.
|2006
SYN|Df(2L)GpdHA
OAB|@Df(2L)x528@/@Df(2L)GpdhA@ embryos show a loss of neuroblasts NB1-1,
|NB2-5 and NB2-4. This loss is much more pronounced in odd-numbered
|than even-numbered abdominal segments. However, the loss is similar
|to @mid@ mutants, suggesting that the it is deletion of the @mid@ gene
|and not the @H15@ gene that is causing the phenotype.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0041471	CLA 1 Aberration	GSYM 1 Df(2L)H15-x4	DT 1 30 Oct 06	RESZ 282	REF 1	
ABSY|Df(2L)H15-x4
DT|30 Oct 06
ID|PFab0041471
REF
{
REFM|FBrf0190096
|Buescher et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190096
|Buescher et al.
|2006
SYN|H15<up>x4</up>
PHP|@Df(2L)H15-x4@ embryos show no defects in neuroblast formation.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001475	CLA 1 Aberration	GSYM 1 Df(2L)J2	DT 1 30 Oct 06	RESZ 121	REF 1	
ABSY|Df(2L)J2
DT|30 Oct 06
ID|PFab0001475
REF
{
REFM|FBrf0191242
|Hozumi et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001609	CLA 1 Aberration	GSYM 1 Df(2L)TE35BC-3	DT 1 30 Oct 06	RESZ 127	REF 1	
ABSY|Df(2L)TE35BC-3
DT|30 Oct 06
ID|PFab0001609
REF
{
REFM|FBrf0189924
|Siegrist and Doe
|2005
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001648	CLA 1 Aberration	GSYM 1 Df(2L)TW161	DT 1 30 Oct 06	RESZ 123	REF 1	
ABSY|Df(2L)TW161
DT|30 Oct 06
ID|PFab0001648
REF
{
REFM|FBrf0190740
|Long et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001773	CLA 1 Aberration	GSYM 1 Df(2L)dp-79b	DT 1 30 Oct 06	RESZ 125	REF 1	
ABSY|Df(2L)dp-79b
DT|30 Oct 06
ID|PFab0001773
REF
{
REFM|FBrf0189911
|Hallem and Carlson
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900023	CLA 1 Aberration	GSYM 1 Df(2L)iHog<up>KG</up>	DT 1 30 Oct 06	RESZ 703	REF 1	
ABSY|Df(2L)iHog<up>KG</up>
DT|30 Oct 06
ID|PFab0900023
REF
{
REFM|FBrf0189929
|Yao et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0189929
|Yao et al.
|2006
ACLA|chromosomal_deletion ; SO:1000029
MU|P-element activity
PRG|P{SUPor-P}CG10158<up>KG05348</up>
ASAL|CG10158<up>KG</up>
|iHog<up>KG</up>
AMD|iHog
AMP|CG10158 (molecular determination)
OTH|Imprecise excision of the @P{SUPor-P}@ element, resulting in deletion
|from +1979 of the @iHog@ coding sequence to the original @P{SUPor-P}@
|insertion site. This removes the sequence encoding the transmembrane
|domain of the @iHog@ protein and some of the 5'UTR of the @CG10158@
|gene.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0001905	CLA 1 Aberration	GSYM 1 Df(2L)sc19-1	DT 1 30 Oct 06	RESZ 232	REF 1	
ABSY|Df(2L)sc19-1
DT|30 Oct 06
ID|PFab0001905
REF
{
REFM|FBrf0190186
|Yu et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190186
|Yu et al.
|2006
SYN|Df(2L)sc19-1
AMD|Msp-300
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0041478	CLA 1 Aberration	GSYM 1 Df(2L)x528	DT 1 30 Oct 06	RESZ 539	REF 1	
ABSY|Df(2L)x528
DT|30 Oct 06
ID|PFab0041478
REF
{
REFM|FBrf0190096
|Buescher et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190096
|Buescher et al.
|2006
OAB|@Df(2L)x528@/@Df(2L)GpdhA@ embryos show a loss of neuroblasts NB1-1,
|NB2-5 and NB2-4. This loss is much more pronounced in odd-numbered
|than even-numbered abdominal segments. However, the loss is similar
|to @mid@ mutants, suggesting that the it is deletion of the @mid@ gene
|and not the @H15@ gene that is causing the phenotype.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900024	CLA 1 Aberration	GSYM 1 Df(2R)&Dgr;5-22	DT 1 30 Oct 06	RESZ 133	REF 1	
ABSY|Df(2R)&Dgr;5-22
DT|30 Oct 06
ID|PFab0900024
REF
{
REFM|-1709519654
|Park
|2006
|-1
|Curr. Biol. 16: 1154--1159
}

ASAL|CheB42a<up>&Dgr;5-22</up>
}
# EOR
ABSR
{
RETE|ID 1 PFab0000001	CLA 1 Aberration	GSYM 1 Df(2R)03072	DT 1 30 Oct 06	RESZ 209	REF 1	
ABSY|Df(2R)03072
DT|30 Oct 06
ID|PFab0000001
REF
{
REFM|FBrf0190559
|Roignant et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190559
|Roignant et al.
|2006
SYN|Df(2R)03072
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900025	CLA 1 Aberration	GSYM 1 Df(2R)Alk-21	DT 1 30 Oct 06	RESZ 599	REF 2	
ABSY|Df(2R)Alk-21
DT|30 Oct 06
ID|PFab0900025
REF
{
REFM|FBrf0162095
|Loren et al.
|2003
|-1
REFM|-775664496
|Loren
|2003
|-1
|EMBO Rpts 4: http://www.nature.com/embor/journal/v4/n8/index.html
}

REFDSR
{
RDID|FBrf0162095
|Loren et al.
|2003
SYN|Df(2R)Alk&Dgr;21
AMD|Alk
}

REFDSR
{
RDID|-775664496
|Loren
|2003
SYN|Df(2R)DAlk21
BPT|P{lacW}Cdk4<up>k06503</up>;P{lacW}E10-2-40
ACLA|chromosomal_deletion ; SO:1000029
MU|P-element activity
PRG|P{lacW}Cdk4<up>k06503</up>
|P{lacW}E10-2-40
OTH|Approximately 245kb deletion.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900026	CLA 1 Aberration	GSYM 1 Df(2R)BSC161	DT 1 30 Oct 06	RESZ 762	REF 1	
ABSY|Df(2R)BSC161
DT|30 Oct 06
ID|PFab0900026
REF
{
REFM|-1742651862
|Christensen
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651862
|Christensen
|2006.8.29
SYN|Df(2R)BSC161
BPT|PBac{WH}mbl<up>f06658</up>;P{XP}CG30104<up>d00824</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2R)BSC161@ predicted from the Release
|4 genomic coordinates of the progenitor @PBac{WH}mbl<up>f06658</up>@ and @P{XP}CG30104<up>d00824</up>@
|insertion sites are 54B2;54B17.
MU|FLPase
PRG|PBac{WH}mbl<up>f06658</up>
|P{XP}CG30104<up>d00824</up>
AMD|cnk
OTH|Presence of @P+PBac{XP5.WH5}BSC161@ was verified using the PCR methods
|and primers described in FBrf0175003.
TRNA|P+PBac{XP5.WH5}BSC161
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900027	CLA 1 Aberration	GSYM 1 Df(2R)BSC199	DT 1 30 Oct 06	RESZ 864	REF 1	
ABSY|Df(2R)BSC199
DT|30 Oct 06
ID|PFab0900027
REF
{
REFM|-1742651840
|Christensen
|2006.8.30
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1742651840
|Christensen
|2006.8.30
SYN|Df(2R)BSC199
BPT|P{XP}d10427;PBac{RB}Oda<up>e03814</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(2R)BSC199@ predicted from the progenitor
|@P{XP}d10427@ and @PBac{RB}Oda<up>e03814</up>@ insertions sites using Release
|4 coordinates are 48D1;48E4.
MU|FLPase
PRG|P{XP}d10427
|PBac{RB}Oda<up>e03814</up>
AMD|jeb
OTH|Presence of @Df(2R)BSC199@ was verified using the PCR methods and primers
|described in FBrf0175003 with the substitution of the primer 5'-CCAATGCGTTTATTTCAGGTCACG-3'
|for the RB3' plus or RB3' minus primer in the Hybrid PCR protocol in
|the Supplementary Methods.
TRNA|P+PBac{XP5.RB3}BSC199
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0029979	CLA 1 Aberration	GSYM 1 Df(2R)BSC29	DT 1 30 Oct 06	RESZ 384	REF 2	
ABSY|Df(2R)BSC29
DT|30 Oct 06
ID|PFab0029979
REF
{
REFM|FBrf0190611
|Kittel et al.
|2006
|-1
REFM|-1318817562
|Kittel
|2006
|-1
|Science 312: http://www.sciencemag.org/cgi/content/full/1126308/DC1
}

REFDSR
{
RDID|FBrf0190611
|Kittel et al.
|2006
SYN|Df(2R)BSC29
}

REFDSR
{
RDID|-1318817562
|Kittel
|2006
SYN|Df(2R)BSC29
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038075	CLA 1 Aberration	GSYM 1 Df(2R)Exel8057	DT 1 30 Oct 06	RESZ 361	REF 1	
ABSY|Df(2R)Exel8057
DT|30 Oct 06
ID|PFab0038075
REF
{
REFM|936899289
|Sanchez
|2006
|-1
|Curr. Biol. 16: http://www.current-biology.com/cgi/content/full/16/7/680/DC1/
}

REFDSR
{
RDID|936899289
|Sanchez
|2006
SYN|Df(2R)Exel 8057
AMD|CG13323
|CG4630
|GLaz
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900028	CLA 1 Aberration	GSYM 1 Df(2R)Rpn6<up>2F</up>	DT 1 30 Oct 06	RESZ 416	REF 1	
ABSY|Df(2R)Rpn6<up>2F</up>
DT|30 Oct 06
ID|PFab0900028
REF
{
REFM|FBrf0190559
|Roignant et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190559
|Roignant et al.
|2006
SYN|Df(Rpn6)<up>2F</up>
BPT|51C2;51C5
ASAL|CG10151<up>2F</up>
|Rpn6<up>2F</up>
AMD|ave
AMP|Rpn (molecular determination)
|CG10151 (molecular determination)
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002055	CLA 1 Aberration	GSYM 1 Df(2R)X58-7	DT 1 30 Oct 06	RESZ 197	REF 1	
ABSY|Df(2R)X58-7
DT|30 Oct 06
ID|PFab0002055
REF
{
REFM|FBrf0189906
|Dickman et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0189906
|Dickman et al.
|2005
SYN|Df(2R)x58-7
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002178	CLA 1 Aberration	GSYM 1 Df(2R)exu1	DT 1 30 Oct 06	RESZ 121	REF 1	
ABSY|Df(2R)exu1
DT|30 Oct 06
ID|PFab0002178
REF
{
REFM|FBrf0189914
|Li and Carthew
|2005
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900029	CLA 1 Aberration	GSYM 1 Df(2R)mir-7-&Dgr;1	DT 1 30 Oct 06	RESZ 574	REF 1	
ABSY|Df(2R)mir-7-&Dgr;1
DT|30 Oct 06
ID|PFab0900029
REF
{
REFM|FBrf0189914
|Li and Carthew
|2005
|-1
}

REFDSR
{
RDID|FBrf0189914
|Li and Carthew
|2005
ACLA|chromosomal_deletion ; SO:1000029
MU|P-element activity
PRG|bl<up>EP954</up>
AM|Deletes mir-7 (molecular determination)
AMP|Hil (molecular determination)
|bl (molecular determination)
PHP|Eye development is normal in @Df(2R)mir-7-&Dgr;1@ flies.
OTH|A 6.8kb deletion that removes @mir-7@, the last two exons of @bl@ and
|two exons of @Hil@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002231	CLA 1 Aberration	GSYM 1 Df(2R)trix	DT 1 30 Oct 06	RESZ 655	REF 1	
ABSY|Df(2R)trix
DT|30 Oct 06
ID|PFab0002231
REF
{
REFM|FBrf0190149
|O'Dor et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190149
|O'Dor et al.
|2006
SYN|Df(trix)
PHP|@Df(2R)trix@ embryos from heterozygous mothers show segregation defects
|in anaphase and telophase as judged by the presence of chromatin bridges.
|These embryos show a higher level of "nuclear fallout", a process
|that removes nuclei with abnormal mitoses, than wild-type embryos.
|Fallout nuclei tend to be observed in pairs or clusters. There is
|no evidence of metaphase defects in these embryos and have a late telophase
|appearance.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0000011	CLA 1 Aberration	GSYM 1 Df(3L)81k19	DT 1 30 Oct 06	RESZ 222	REF 1	
ABSY|Df(3L)81k19
DT|30 Oct 06
ID|PFab0000011
REF
{
REFM|1094425008
|Kennison
|2006.7.21
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|1094425008
|Kennison
|2006.7.21
SYN|Df(3L)81k19
AMDD|cp
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900030	CLA 1 Aberration	GSYM 1 Df(3L)BSC170	DT 1 30 Oct 06	RESZ 622	REF 1	
ABSY|Df(3L)BSC170
DT|30 Oct 06
ID|PFab0900030
REF
{
REFM|-1516148577
|Gresens
|2006.7.11
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1516148577
|Gresens
|2006.7.11
SYN|Df(3L)BSC170
BPT|P{XP}Argk<up>d07847</up>;PBac{WH}Rdl<up>f02994</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(3L)BSC170@ predicted from the @P{XP}Argk<up>d07847</up>@
|and @PBac{WH}Rdl<up>f02994</up>@ insertions sites using Release 4 are 66F4;67A1.
PRG|P{XP}Argk<up>d07847</up>
|PBac{WH}Rdl<up>f02994</up>
COR|FLPase
AMD|bol
|Rdl
TRNA|P+PBac{XP5.WH5}BSC170
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900031	CLA 1 Aberration	GSYM 1 Df(3L)BSC178	DT 1 30 Oct 06	RESZ 727	REF 1	
ABSY|Df(3L)BSC178
DT|30 Oct 06
ID|PFab0900031
REF
{
REFM|-1516118747
|Gresens
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1516118747
|Gresens
|2006.8.29
SYN|Df(3L)BSC178
BPT|P{XP}Ptp61F<up>d07829</up>;PBac{RB}CG12090<up>e00227</up>
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(3L)BSC178@ predicted from the progenitor
|@P{XP}Ptp61F<up>d07829</up>@ and @PBac{RB}CG12090<up>e00227</up>@ insertions sites
|using Release 4 coordinates are 61F8;62A4.
MU|FLPase
PRG|P{XP}Ptp61F<up>d07829</up>
|PBac{RB}CG12090<up>e00227</up>
AMD|cue
OAB|Inferred to overlap with: @Df(3L)Exel6087@.
|Fails to complement @Df(3L)Exel6087@.
TRNA|P+PBac{XP5.RB3}BSC178
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0028099	CLA 1 Aberration	GSYM 1 Df(3L)E1	DT 1 30 Oct 06	RESZ 116	REF 1	
ABSY|Df(3L)E1
DT|30 Oct 06
ID|PFab0028099
REF
{
REFM|FBrf0189896
|Ashraf et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0035340	CLA 1 Aberration	GSYM 1 Df(3L)ED230	DT 1 30 Oct 06	RESZ 213	REF 1	
ABSY|Df(3L)ED230
DT|30 Oct 06
ID|PFab0035340
REF
{
REFM|FBrf0190027
|Kwon and Montell
|2006
|-1
}

REFDSR
{
RDID|FBrf0190027
|Kwon and Montell
|2006
SYN|Df(3L)ED230
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0036023	CLA 1 Aberration	GSYM 1 Df(3L)ED4782	DT 1 30 Oct 06	RESZ 231	REF 1	
ABSY|Df(3L)ED4782
DT|30 Oct 06
ID|PFab0036023
REF
{
REFM|309552619
|Mathew
|2005
|-1
|Science: http://www.sciencemag.org/cgi/data/310/5752/1344/DC1/1
}

REFDSR
{
RDID|309552619
|Mathew
|2005
SYN|Dfdfz2
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038107	CLA 1 Aberration	GSYM 1 Df(3L)Exel6087	DT 1 30 Oct 06	RESZ 277	REF 1	
ABSY|Df(3L)Exel6087
DT|30 Oct 06
ID|PFab0038107
REF
{
REFM|-1516118747
|Gresens
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1516118747
|Gresens
|2006.8.29
SYN|Df(3L)Exel6087
OAB|Inferred to overlap with: @Df(3L)BSC178@.
|Fails to complement @Df(3L)BSC178@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038155	CLA 1 Aberration	GSYM 1 Df(3L)Exel6135	DT 1 30 Oct 06	RESZ 455	REF 1	
ABSY|Df(3L)Exel6135
DT|30 Oct 06
ID|PFab0038155
REF
{
REFM|FBrf0190051
|Wang et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190051
|Wang et al.
|2006
PHP|@Df(3L)Exel6135@ embryos, which lack ten genes including @LCBP1@ and
|@serp@ exhibit more severe tube-overextension phenotypes that either
|@LCBP1@ or @serp@ mutants. These mutants also exhibit a slight diametric
|overgrowth in the tracheal dorsal trunk.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0026852	CLA 1 Aberration	GSYM 1 Df(3L)HnD-1	DT 1 30 Oct 06	RESZ 205	REF 1	
ABSY|Df(3L)HnD-1
DT|30 Oct 06
ID|PFab0026852
REF
{
REFM|FBrf0190154
|Reddy et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190154
|Reddy et al.
|2006
SYN|Df(3L)HnD-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0028493	CLA 1 Aberration	GSYM 1 Df(3L)XS543	DT 1 30 Oct 06	RESZ 123	REF 1	
ABSY|Df(3L)XS543
DT|30 Oct 06
ID|PFab0028493
REF
{
REFM|FBrf0190051
|Wang et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0028495	CLA 1 Aberration	GSYM 1 Df(3L)XS705	DT 1 30 Oct 06	RESZ 123	REF 1	
ABSY|Df(3L)XS705
DT|30 Oct 06
ID|PFab0028495
REF
{
REFM|FBrf0190051
|Wang et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0029480	CLA 1 Aberration	GSYM 1 Df(3L)bab<up>Ar07</up>	DT 1 30 Oct 06	RESZ 163	REF 1	
ABSY|Df(3L)bab<up>Ar07</up>
DT|30 Oct 06
ID|PFab0029480
REF
{
REFM|-1385577196
|Jeong
|2006
|-1
|Cell 125: 1387--1399
}

REFDSR
{
RDID|-1385577196
|Jeong
|2006
SYN|bab<up>Ar07</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002383	CLA 1 Aberration	GSYM 1 Df(3L)kto2	DT 1 30 Oct 06	RESZ 220	REF 1	
ABSY|Df(3L)kto2
DT|30 Oct 06
ID|PFab0002383
REF
{
REFM|1094425008
|Kennison
|2006.7.21
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|1094425008
|Kennison
|2006.7.21
SYN|Df(3L)kto2
AMDD|cp
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002387	CLA 1 Aberration	GSYM 1 Df(3L)lxd6	DT 1 30 Oct 06	RESZ 541	REF 2	
ABSY|Df(3L)lxd6
DT|30 Oct 06
ID|PFab0002387
REF
{
REFM|FBrf0189899
|Bartscherer et al.
|2006
|-1
REFM|FBrf0190159
|Scuderi et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0189899
|Bartscherer et al.
|2006
AMD|srt
}

REFDSR
{
RDID|FBrf0190159
|Scuderi et al.
|2006
SYN|Df(3L)lxd6
OAB|@Df(3L)lxd6@/@Df(3L)vin4@ transheterozygotes show the same head involution
|defects as @Df(3L)vin4@ homozygotes.
PHP|@Df(3L)lxd6@ flies develop show no visible phenotype.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900032	CLA 1 Aberration	GSYM 1 Df(3L)melt-&Dgr;1	DT 1 30 Oct 06	RESZ 575	REF 1	
ABSY|Df(3L)melt-&Dgr;1
DT|30 Oct 06
ID|PFab0900032
REF
{
REFM|FBrf0187233
|Mikeladze-Dvali et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0187233
|Mikeladze-Dvali et al.
|2005
DIS|A.A. Teleman
ASAL|corn<up>&Dgr;1</up>
AM|Deletes melt (molecular determination)
|Deletes CG32390 (molecular determination)
AMP|corn (molecular determination)
PHP|@Df(3L)melt-&Dgr;1@ eyes show a loss of pR8 cells and an expansion
|of yR8 cells.
|@Df(3L)melt-&Dgr;1@ R7 photoreceptor cell clones do not affect the
|fate of R8 photoreceptor cells.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900033	CLA 1 Aberration	GSYM 1 Df(3L)melt-&Dgr;3	DT 1 30 Oct 06	RESZ 330	REF 1	
ABSY|Df(3L)melt-&Dgr;3
DT|30 Oct 06
ID|PFab0900033
REF
{
REFM|FBrf0187233
|Mikeladze-Dvali et al.
|2005
|-1
}

ASAL|corn<up>&Dgr;3</up>
AMD|melt
|CG32390
AMP|corn
PHP|@Df(3L)melt-&Dgr;3@ eyes show a loss of pR8 cells and an expansion
|of yR8 cells.
}
# EOR
ABSR
{
RETE|ID 1 PFab0002392	CLA 1 Aberration	GSYM 1 Df(3L)rdgC-co2	DT 1 30 Oct 06	RESZ 513	REF 1	
ABSY|Df(3L)rdgC-co2
DT|30 Oct 06
ID|PFab0002392
REF
{
REFM|1094425008
|Kennison
|2006.7.21
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|1094425008
|Kennison
|2006.7.21
SYN|Df(3L)rdgC-co2
CCM|Previously reported to delete @cp@, however this was due to @Df(3L)rdgC-co2@
|chromosome carrying @cp<up>1</up>@. @cp<up>1</up>@ is separable from @Df(3L)rdgC-co2@
|by recombination.
COR|Induced on: marked third chromosome that carried the @cp<up>1</up>@ allele.
AMDD|cp
MK|cp<up>1</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002454	CLA 1 Aberration	GSYM 1 Df(3L)vin2	DT 1 30 Oct 06	RESZ 562	REF 1	
ABSY|Df(3L)vin2
DT|30 Oct 06
ID|PFab0002454
REF
{
REFM|FBrf0190159
|Scuderi et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190159
|Scuderi et al.
|2006
SYN|Df(3L)vin2
PHP|@Df(3L)vin2@ mutants show defects in head involution. The mouth hooks
|are present but the labrum and epistomal sclerites are missing and
|at least part of the cephalopharyngeal skeleton remains at the surface
|of the embryo.
|@Df(3L)vin2@ embryos show reduced levels of cell death, as evidenced
|by lower levels of @decay@ protein activity.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002456	CLA 1 Aberration	GSYM 1 Df(3L)vin4	DT 1 30 Oct 06	RESZ 680	REF 1	
ABSY|Df(3L)vin4
DT|30 Oct 06
ID|PFab0002456
REF
{
REFM|FBrf0190159
|Scuderi et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190159
|Scuderi et al.
|2006
SYN|Df(3L)vin4
OAB|@Df(3L)lxd6@/@Df(3L)vin4@ transheterozygotes show the same head involution
|defects as @Df(3L)vin4@ homozygotes.
PHP|@Df(3L)vin4@ mutants show defects in head involution. The mouth hooks
|are present but the labrum and epistomal sclerites are missing and
|at least part of the cephalopharyngeal skeleton remains at the surface
|of the embryo.
|@Df(3L)vin4@ embryos show reduced levels of cell death, as evidenced
|by lower levels of @decay@ protein activity.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900034	CLA 1 Aberration	GSYM 1 Df(3R)BSC198	DT 1 30 Oct 06	RESZ 579	REF 1	
ABSY|Df(3R)BSC198
DT|30 Oct 06
ID|PFab0900034
REF
{
REFM|-1516118747
|Gresens
|2006.8.29
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-1516118747
|Gresens
|2006.8.29
SYN|Df(3R)BSC198
BPT|PBac{WH}f02841;P{XP}d04754
ACLA|chromosomal_deletion ; SO:1000029
CCM|The cytological breakpoints of @Df(3R)BSC198@ predicted from the progenitor
|@PBac{WH}f02841@ and @P{XP}d04754@ insertion sites using Release 4
|coordinates are 84F13;85A2.
MU|FLPase
PRG|PBac{WH}f02841
|P{XP}d04754
AMD|l(3)84Fk
|stck
TRNA|P+PBac{XP5.WH5}BSC198
MK|w<up>-</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002515	CLA 1 Aberration	GSYM 1 Df(3R)D605	DT 1 30 Oct 06	RESZ 1163	REF 1	
ABSY|Df(3R)D605
DT|30 Oct 06
ID|PFab0002515
REF
{
REFM|FBrf0189912
|Kocks et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0189912
|Kocks et al.
|2005
SYN|Df(3R)D605
AMD|eater
OAB|@Df(3R)Tl-I@/@Df(3R)D605@ flies are viable and fertile.
|@Df(3R)Tl-I@/@Df(3R)D605@ hemocytes show impaired levels of phagocytosis
|of both gram-positive and gram-negative bacteria, but show wild-type
|levels of phagocytosis of india ink carbon particles. These hemocytes
|appear to adhere less tightly to the larval cuticle than wild-type
|hemocytes.
|@Df(3R)Tl-I@/@Df(3R)D605@ flies show strongly impaired levels of phagocytosis
|of gram-positive bacteria compared to wild-type or heterozygous controls.
|These flies also show an impairment in phagocytosis of gram-negative
|bacteria, although to a lesser extent.
|@Df(3R)Tl-I@/@Df(3R)D605@ flies show a normal humoral response.
|After feeding on gram-negative bacteria, @Df(3R)Tl-I@/@Df(3R)D605@
|flies die more rapidly than wild-type flies. The hemolymph of these
|flies contains about a 10,000-fold increase in bacterial number compared
|to wild-type flies.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0036742	CLA 1 Aberration	GSYM 1 Df(3R)ED5506	DT 1 30 Oct 06	RESZ 348	REF 1	
ABSY|Df(3R)ED5506
DT|30 Oct 06
ID|PFab0036742
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)ED5506
BPT|86C7;86D5
ACLA|chromosomal_deletion ; SO:1000029
AMD|cu
OAB|Lethal in combination with @Df(3R)MS32@.
|Inferred to overlap with: @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0036748	CLA 1 Aberration	GSYM 1 Df(3R)ED5514	DT 1 30 Oct 06	RESZ 406	REF 1	
ABSY|Df(3R)ED5514
DT|30 Oct 06
ID|PFab0036748
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)ED5514
BPT|86C7;86E11
ACLA|chromosomal_deletion ; SO:1000029
AMD|cu
|RpS25
|RpL3
OAB|Lethal in combination with @Df(3R)MS32@.
|Inferred to overlap with: @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0036749	CLA 1 Aberration	GSYM 1 Df(3R)ED5516	DT 1 30 Oct 06	RESZ 229	REF 1	
ABSY|Df(3R)ED5516
DT|30 Oct 06
ID|PFab0036749
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)ED5516
OAB|Viable in combination with @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0036751	CLA 1 Aberration	GSYM 1 Df(3R)ED5518	DT 1 30 Oct 06	RESZ 406	REF 1	
ABSY|Df(3R)ED5518
DT|30 Oct 06
ID|PFab0036751
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)ED5518
BPT|86C7;86E13
ACLA|chromosomal_deletion ; SO:1000029
AMD|cu
|RpS25
|RpL3
OAB|Lethal in combination with @Df(3R)MS32@.
|Inferred to overlap with: @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002570	CLA 1 Aberration	GSYM 1 Df(3R)Espl3	DT 1 30 Oct 06	RESZ 227	REF 1	
ABSY|Df(3R)Espl3
DT|30 Oct 06
ID|PFab0002570
REF
{
REFM|1273889107
|Jiang
|2006
|-1
|Molec. Cell. Biol. 26: 6547--6556
}

REFDSR
{
RDID|1273889107
|Jiang
|2006
SYN|Df(3R)Espl3
AMD|dys
|gro
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038214	CLA 1 Aberration	GSYM 1 Df(3R)Exel6159	DT 1 30 Oct 06	RESZ 352	REF 1	
ABSY|Df(3R)Exel6159
DT|30 Oct 06
ID|PFab0038214
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)Exel6159
BPT|86C3;86C7
ACLA|chromosomal_deletion ; SO:1000029
AMD|cu
OAB|Lethal in combination with @Df(3R)MS32@.
|Inferred to overlap with: @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038259	CLA 1 Aberration	GSYM 1 Df(3R)Exel6204	DT 1 30 Oct 06	RESZ 179	REF 1	
ABSY|Df(3R)Exel6204
DT|30 Oct 06
ID|PFab0038259
REF
{
REFM|1273889107
|Jiang
|2006
|-1
|Molec. Cell. Biol. 26: 6547--6556
}

REFDSR
{
RDID|1273889107
|Jiang
|2006
SYN|Df(3R)Exel6204
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038301	CLA 1 Aberration	GSYM 1 Df(3R)Exel7308	DT 1 30 Oct 06	RESZ 233	REF 1	
ABSY|Df(3R)Exel7308
DT|30 Oct 06
ID|PFab0038301
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)Exel7308
OAB|Viable in combination with @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0038340	CLA 1 Aberration	GSYM 1 Df(3R)Exel9018	DT 1 30 Oct 06	RESZ 233	REF 1	
ABSY|Df(3R)Exel9018
DT|30 Oct 06
ID|PFab0038340
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)Exel9018
OAB|Viable in combination with @Df(3R)MS32@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002581	CLA 1 Aberration	GSYM 1 Df(3R)GC14	DT 1 30 Oct 06	RESZ 230	REF 1	
ABSY|Df(3R)GC14
DT|30 Oct 06
ID|PFab0002581
REF
{
REFM|FBrf0190104
|Clark et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190104
|Clark et al.
|2006
SYN|Df(3R)GC14
AMD|tin
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900035	CLA 1 Aberration	GSYM 1 Df(3R)MS32	DT 1 30 Oct 06	RESZ 862	REF 1	
ABSY|Df(3R)MS32
DT|30 Oct 06
ID|PFab0900035
REF
{
REFM|-280067813
|Cook
|2006.10.01
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|-280067813
|Cook
|2006.10.01
SYN|Df(3R)MS32
BPT|86C8--86C13;86D8--86E1
ACLA|chromosomal_deletion ; SO:1000029
CCM|The 86C7,8 doublet is present, 86C13 is absent, 86D8 is absent and
|the 86E1,2 doublet is present.
AMD|cu
AMDD|pros
OAB|Viable in combination with @Df(3R)Exel9018@, @Df(3R)Exel7308@ and @Df(3R)ED5516@.
|Lethal in combination with @Df(3R)ED5506@.
|Inferred to overlap with: @Df(3R)ED5506@.
|Lethal in combination with @Df(3R)Exel6159@.
|Inferred to overlap with: @Df(3R)Exel6159@.
|Lethal in combination with @Df(3R)ED5514@.
|Inferred to overlap with: @Df(3R)ED5514@.
|Lethal in combination with @Df(3R)ED5518@.
|Inferred to overlap with: @Df(3R)ED5518@.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002664	CLA 1 Aberration	GSYM 1 Df(3R)Tl-I	DT 1 30 Oct 06	RESZ 1164	REF 1	
ABSY|Df(3R)Tl-I
DT|30 Oct 06
ID|PFab0002664
REF
{
REFM|FBrf0189912
|Kocks et al.
|2005
|-1
}

REFDSR
{
RDID|FBrf0189912
|Kocks et al.
|2005
SYN|Df(3R)Tl-I
AMD|eater
OAB|@Df(3R)Tl-I@/@Df(3R)D605@ flies are viable and fertile.
|@Df(3R)Tl-I@/@Df(3R)D605@ hemocytes show impaired levels of phagocytosis
|of both gram-positive and gram-negative bacteria, but show wild-type
|levels of phagocytosis of india ink carbon particles. These hemocytes
|appear to adhere less tightly to the larval cuticle than wild-type
|hemocytes.
|@Df(3R)Tl-I@/@Df(3R)D605@ flies show strongly impaired levels of phagocytosis
|of gram-positive bacteria compared to wild-type or heterozygous controls.
|These flies also show an impairment in phagocytosis of gram-negative
|bacteria, althoughh to a lesser extent.
|@Df(3R)Tl-I@/@Df(3R)D605@ flies show a normal humoral response.
|After feeding on gram-negative bacteria, @Df(3R)Tl-I@/@Df(3R)D605@
|flies die more rapidly than wild-type flies. The hemolymph of these
|flies contains about a 10,000-fold increase in bacterial number compared
|to wild-type flies.
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002668	CLA 1 Aberration	GSYM 1 Df(3R)Tl-X	DT 1 30 Oct 06	RESZ 216	REF 1	
ABSY|Df(3R)Tl-X
DT|30 Oct 06
ID|PFab0002668
REF
{
REFM|FBrf0190486
|sm55 == LeMosy
|2006
|-1
}

REFDSR
{
RDID|FBrf0190486
|sm55 == LeMosy
|2006
SYN|Tl<up>9QRX</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002762	CLA 1 Aberration	GSYM 1 Df(3R)dsx3	DT 1 30 Oct 06	RESZ 125	REF 1	
ABSY|Df(3R)dsx3
DT|30 Oct 06
ID|PFab0002762
REF
{
REFM|FBrf0190088
|Barmina et al.
|2005
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002766	CLA 1 Aberration	GSYM 1 Df(3R)dsx43	DT 1 30 Oct 06	RESZ 124	REF 1	
ABSY|Df(3R)dsx43
DT|30 Oct 06
ID|PFab0002766
REF
{
REFM|FBrf0190731
|Ji and Clark
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0024887	CLA 1 Aberration	GSYM 1 Df(3R)ea-5022rx1	DT 1 30 Oct 06	RESZ 225	REF 1	
ABSY|Df(3R)ea-5022rx1
DT|30 Oct 06
ID|PFab0024887
REF
{
REFM|FBrf0190486
|sm55 == LeMosy
|2006
|-1
}

REFDSR
{
RDID|FBrf0190486
|sm55 == LeMosy
|2006
SYN|ea<up>5022rx1</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002811	CLA 1 Aberration	GSYM 1 Df(3R)kar-Sz11	DT 1 30 Oct 06	RESZ 252	REF 1	
ABSY|Df(3R)kar-Sz11
DT|30 Oct 06
ID|PFab0002811
REF
{
REFM|FBrf0190115
|Dussillol-Godar et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190115
|Dussillol-Godar et al.
|2006
SYN|Df(3R)kar<up>SZ11</up>
|Df(3R)karSZ11
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0002886	CLA 1 Aberration	GSYM 1 Df(3R)ro-XB3	DT 1 30 Oct 06	RESZ 223	REF 1	
ABSY|Df(3R)ro-XB3
DT|30 Oct 06
ID|PFab0002886
REF
{
REFM|FBrf0190486
|sm55 == LeMosy
|2006
|-1
}

REFDSR
{
RDID|FBrf0190486
|sm55 == LeMosy
|2006
SYN|Df(3R)ro<up>XB3</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0900036	CLA 1 Aberration	GSYM 1 Df(4)Eph<up>x652</up>	DT 1 30 Oct 06	RESZ 426	REF 1	
ABSY|Df(4)Eph<up>x652</up>
DT|30 Oct 06
ID|PFab0900036
REF
{
REFM|FBrf0190278
|Boyle et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190278
|Boyle et al.
|2006
ACLA|chromosomal_deletion ; SO:1000029
MU|&Dgr;2-3
PRG|P{hsp26-pt-T}P114
ASAL|Eph<up>x652</up>
|onecut<up>x652</up>
AMP|Eph (molecular determination)
|onecut (molecular determination)
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0009786	CLA 1 Aberration	GSYM 1 Dp(2;2)dpp<up>d21</up>	RESZ 109	REF 1	
ABSY|Dp(2;2)dpp<up>d21</up>
ID|PFab0009786
REF
{
REFM|FBrf0189911
|Hallem and Carlson
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0037620	CLA 1 Aberration	GSYM 1 Dp(3;3)p53<up>-ns</up>	DT 1 30 Oct 06	RESZ 289	REF 1	
ABSY|Dp(3;3)p53<up>-ns</up>
DT|30 Oct 06
ID|PFab0037620
REF
{
REFM|FBrf0190489
|sm53 == Rebollar et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190489
|sm53 == Rebollar et al.
|2006
SYN|Dmp53<up>null</up>
ASAL|p53<up>-ns.3'</up>
|p53<up>-ns.5'</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0004696	CLA 1 Aberration	GSYM 1 In(2L)t	DT 1 30 Oct 06	RESZ 139	REF 1	
ABSY|In(2L)t
DT|30 Oct 06
ID|PFab0004696
REF
{
REFM|95392262
|Zurovcova
|2006
|-1
|Gene 381: 24--33
}

REFDSR
{
RDID|95392262
|Zurovcova
|2006
SYN|In(2L)t
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0008032	CLA 1 Aberration	GSYM 1 T(2;3)rdgC<up>co6</up>	DT 1 30 Oct 06	RESZ 227	REF 1	
ABSY|T(2;3)rdgC<up>co6</up>
DT|30 Oct 06
ID|PFab0008032
REF
{
REFM|1094425008
|Kennison
|2006.7.21
|-1
|personal communication to FlyBase
}

REFDSR
{
RDID|1094425008
|Kennison
|2006.7.21
SYN|T(2;3)rdgC<up>co6</up>
MK|cp<up>1</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0008849	CLA 1 Aberration	GSYM 1 T(Y;3)Antp<up>Ns-rv3</up>	DT 1 30 Oct 06	RESZ 142	REF 1	
ABSY|T(Y;3)Antp<up>Ns-rv3</up>
DT|30 Oct 06
ID|PFab0008849
REF
{
REFM|FBrf0190260
|Vef et al.
|2006
|-1
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0009478	CLA 1 Aberration	GSYM 1 Tp(1;2)sc<up>19</up>	DT 1 30 Oct 06	RESZ 230	REF 1	
ABSY|Tp(1;2)sc<up>19</up>
DT|30 Oct 06
ID|PFab0009478
REF
{
REFM|FBrf0190277
|Bossing and Brand
|2006
|-1
}

REFDSR
{
RDID|FBrf0190277
|Bossing and Brand
|2006
SYN|Tp(1;2)sc19
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0009726	CLA 1 Aberration	GSYM 1 Tp(2;1)B19	DT 1 30 Oct 06	RESZ 223	REF 1	
ABSY|Tp(2;1)B19
DT|30 Oct 06
ID|PFab0009726
REF
{
REFM|FBrf0190186
|Yu et al.
|2006
|-1
}

REFDSR
{
RDID|FBrf0190186
|Yu et al.
|2006
SYN|Dp(2;1)B19
AMDP|Msp-300
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0010050	CLA 1 Aberration	GSYM 1 Tp(3;3)h<up>M3</up>	DT 1 30 Oct 06	RESZ 169	REF 1	
ABSY|Tp(3;3)h<up>M3</up>
DT|30 Oct 06
ID|PFab0010050
REF
{
REFM|-1020697608
|Kim
|2006
|-1
|Biochem. J. 398: 451--460
}

REFDSR
{
RDID|-1020697608
|Kim
|2006
SYN|Tp(3;3)h<up>M3</up>
}

}
# EOR
ABSR
{
RETE|ID 1 PFab0010055	CLA 1 Aberration	GSYM 1 Tp(3;3)kar<up>51</up>	DT 1 30 Oct 06	RESZ 182	REF 1	
ABSY|Tp(3;3)kar<up>51</up>
DT|30 Oct 06
ID|PFab0010055
REF
{
REFM|1273889107
|Jiang
|2006
|-1
|Molec. Cell. Biol. 26: 6547--6556
}

REFDSR
{
RDID|1273889107
|Jiang
|2006
SYN|Df(3R)ME61
}

}
# EOR