A Database of Drosophila Genes & Genomes

 

Aberration Dmel\Df(3R)awd-KRB

General Information
SymbolDmel\Df(3R)awd-KRBSpeciesD. melanogaster
NameFlyBase IDFBab0000009
Feature typechromosomal_deletionCreated / Updated2006-08-22/2006-08-22
Formalized genetic data Med << bk1 << l(3)100CDa << bk2
Sequence coordinates
Deleted segment100D1--100D4
Duplicated segment
Computed Breakpoints include 100D1;100D3-100D4
Breakpoints Inherited  
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Cytological Order
Progenitor
Mutagen
Class of aberration (relative to progenitor)
Breakpoints
100C6-100D1;100D1-100D4
100C6-100C7;100D3-100D4
Causes alleles
Carries alleles
Transposon Insertions
Genetic mapping information
Comments
Breakpoint(s) molecularly mapped
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Left limit of break 1 from non-inclusion of Med (FBrf0086254) Right limit of break 1 from polytene analysis (FBrf0086254) Left limit of break 2 from polytene analysis (FBrf0102610) Right limit of break 2 from polytene analysis (FBrf0086254)
 
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DDBJ /
EMBL /
GenBank
DNA sequence
Protein sequence
Name
 
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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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hide Phenotypic Data
In combination with other aberrations
NOT in combination with other aberrations
Df(3R)awd-KRB homozygous embryos exhibit major disruption of the tracheal network accompanied by ectopic branching and looping, appearance of a few extra branches or "knobs", and migration abnormalities.
Deficient embryos show an uninterpretable mutant midgut phenotype.
Does not give a Minute phenotype when heterozygous.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Has a partially penetrant dominant cuticle phenotype.
Heterozygous embryos sometimes have gaps (consisting of patches of naked cuticle) in the denticle belts.
Homozygous embryos are very abnormal compared to wild-type.
No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.
Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.
Shows no maternal enhancement of dpphr4.
The Df(3R)awd-KRB chromosome does not act as a dominant 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).
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hide Stocks ( 2 )
Bloomington
Kyoto
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Discoverer
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      hide Synonyms & Secondary IDs ( 5 )
      Reported As
      Symbol Synonym
      Df(3R)awd-KRB
      Name Synonym
      Secondary FlyBase IDs
        hide References ( 35 )
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        hide Recent research papers ( 1 )
        Wilson et al., 2006, Genetics 173(3): 1455--1463
        High-resolution mapping of quantitative trait loci affecting increased life span in Drosophila melanogaster. [FBrf0194188]