FB2024_02 , released April 23, 2024
Aberration: Dmel\Df(3R)awd-KRB
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General Information
Symbol
Df(3R)awd-KRB
Species
D. melanogaster
Name
FlyBase ID
FBab0000009
Feature type
chromosomal_deletion
Also Known As
Df(3R)awdKRB, Df(3R)awd
Computed Breakpoints include

100D1;100D3-100D4

Features within 100D1--100D4
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Wisotzkey et al., 1998, Giesen et al., 1997, Salzberg et al., 1997, Duffy et al., 1996, Harbecke and Lengyel, 1995, Raftery, 1995.4.6, Roseman et al., 1995)
Breakpoints

100C;100D

(Giesen et al., 1997, Salzberg et al., 1997, Duffy et al., 1996, Harbecke and Lengyel, 1995, Roseman et al., 1995)

100C6-100D1;100D1-100D4

(Raftery, 1995.4.6)

100C6-100C7;100D3-100D4

(Wisotzkey et al., 1998)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

Med << bk1 << l(3)100CDa << bk2

Genetic mapping information
Comments

Breakpoint(s) molecularly mapped

(Xiong and Montell, 1993)
Comments on Cytology

Ref: FBrf0048096.

(Salzberg et al., 1997)

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)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Genes NOT Deleted / Disrupted
Genes Duplicated
Complementation Data
Completely duplicated
Partially duplicated
Molecular Data
Completely duplicated
Partially duplicated
Genes NOT Duplicated
Complementation Data
 
Molecular Data
 
Affected Genes Inferred by Location
    Phenotypic Data
    In combination with other aberrations
    NOT in combination with other aberrations

    Does not give a Minute phenotype when heterozygous.

    (Cook, 2006.1.31)

    Heterozygous embryos sometimes have gaps (consisting of patches of naked cuticle) in the denticle belts.

    (Desbordes et al., 2005)

    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).

    (Mason et al., 2004)

    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.

    (Dammai et al., 2003)

    Has a partially penetrant dominant cuticle phenotype.

    (Cox et al., 2000)

    Shows dominant enhancement of dominant haltere phenotype caused by Ubx195 and Ubx9.22.

    (Burnette et al., 1999)

    No second site non-complementing phenotype with zipEbr and zipmhc-c6.1.

    (Halsell and Kiehart, 1998)

    Shows no maternal enhancement of dpphr4.

    (Nicholls and Gelbart, 1998)

    Dominantly causes tergite defects in less than 50% of run3 heterozygotes.

    (Duffy et al., 1996)

    Deficient embryos show an uninterpretable mutant midgut phenotype.

    (Bilder and Scott, 1995)

    Homozygous embryos are very abnormal compared to wild-type.

    (Harbecke and Lengyel, 1995)
    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (5)
    References (37)