A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(2L)b87e25

General Information
SymbolDmel\Df(2L)b87e25SpeciesD. melanogaster
NameDeficiency (2L) blackFlyBase IDFBab0001747
Feature typechromosomal_deletion
Also Known Asb87e25
Computed Breakpoints include 34C1;35C1
Deleted segment34C1--35C1
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
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hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
34C1-34C2;35B10-35C1
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data bk1 << kuz << vas << bk2 << stc
Genetic mapping information
Comments
hide Comments on Cytology
Ref: Lindsley and Zimm, 1992
Limits of break 1 from polytene analysis (FBrf0053558) Left limit of break 2 from inclusion of vas (FBrf0077941) Right limit of break 2 from polytene analysis (FBrf0080145)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
hide Gene Deletion & Duplication Data
hide Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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Complementation Data
Molecular Data
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In combination with other aberrations
Inferred to overlap with: Df(2L)BSC345.
NOT in combination with other aberrations
Lethal in combination with: Df(2L)BSC147. Inferred to overlap with: Df(2L)BSC147.
Df(2L)b87e25 in combination with a pair of introgressions from D.simulans spanning 30F1-31E7 to 35D7-36A14 Dsim\Int(2L)S and 21A1 to 22D1--23A2 Dsim\Int(2L)D produces semi-sterile male flies. These flies are female sterile.
Suppresses the ommatidial polarity phenotype of dshhs.sev.B. Suppresses the ommatidial polarity phenotype of msnEP549 when driven by Scer\GAL4hs.2sev.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows no maternal enhancement of dpphr4.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Homozygous embryos are very abnormal compared to wild-type.
hide Stocks ( 3 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
The stock contains a second-site deletion uncovering l(2)gl.
hide Balancer / Genotype Variants of the Aberration
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hide Other Comments
The Df(2L)b87e25 chromosome acts as a dominant weak suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion), but this is a false positive result (the suppressor is not within the bounds of the deficient region) because the suppressor maps to the tip of 2L rather than to the site of the deficiency. In addition, the deficiency chromosome fails to complement lethal mutations of l(2)gl.
"irradiation" was stated as tentative. "spontaneous" was stated as tentative.
hide Synonyms & Secondary IDs ( 10 )
Reported As
Symbol Synonym
Df(2L)b80e25
Df(2L)b87a25
Df(2L)b87E25
 
Df(2L)b87e35
Name Synonym
Deficiency (2L) black
 
Secondary FlyBase IDs
hide References ( 37 )
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hide Recent research papers ( 1 )
Weber et al., 2012, Genetics 191(1): 145--162
Novel regulators of planar cell polarity: a genetic analysis in Drosophila. [FBrf0218210]