A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Aberration Dmel\Df(3L)W10

General Information
SymbolDmel\Df(3L)W10SpeciesD. melanogaster
NameDeficiency (3L) WrinkledFlyBase IDFBab0002357
Feature typechromosomal_deletion
Also Known AsDf(3L)WR10, W10, Df(3L)Wr10
Computed Breakpoints include 75A6-75A7;75C2
Deleted segment75A6--75C2
Sequence coordinates
Member of large scale dataset(s)
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Description
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FB2013_03
FB2013_02
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Nature of the Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
75A6-75A7;75C5-75C7
75A6-76A7;75C1-75C2
75B3-75B6;75C1-75C2
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data bk1 << rhea << bk2 << not
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
hide Comments on Cytology
Left limit of break 1 from polytene analysis (FBrf0051843) Right limit of break 1 from polytene analysis (FBrf0082995) Left limit of break 2 from polytene analysis (citation unavailable) Right limit of break 2 from polytene analysis (FBrf0051843)
 
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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
NOT in combination with other aberrations
Dominantly enhances the KrIf-1/+ eye phenotype.
Causes inviability or low viability in hybrid females when heterozygous with D.simulans chromosome.
Intermediate second site non-complementing phenotype with zipEbr and zipmhc-c6.1: malformed phenotype penetrance 25-75%.
Shows no maternal enhancement of dpphr4.
Deficient embryos show a mutant midgut phenotype: posterior constriction forms anterior to normal site, anterior constriction fails to form.
Homozygous embryos do not complete head involution and germband shortening, and tracheae are disrupted. Maintenance of the midgut epithelium, formation of midgut constrictions and elongation of the Malpighian tubules are variable.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Number of cells expressing midline glial cell markers in the embryonic CNS is increased by 60%.
Homozygotes show the full cell death defective phenotype.
75B puff is absent.
hide Stocks ( 2 )
Bloomington
Kyoto
hide Notes on Origin
Discoverer
Segraves.
 
The Cap-H2[TH1] mutation was found on the Df(3L)W10 chromosome.
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hide Synonyms & Secondary IDs ( 13 )
Reported As
Symbol Synonym
Df(3L)W+R
 
Df(3L)Wrv
 
Df(3L)W-R10
 
Name Synonym
Deficiency (3L) Wrinkled
 
Secondary FlyBase IDs
hide References ( 48 )
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