FB2024_03 , released June 25, 2024
Aberration: Dmel\Df(3L)VW3
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General Information
Symbol
Df(3L)VW3
Species
D. melanogaster
Name
FlyBase ID
FBab0002355
Feature type
chromosomal_deletion
Also Known As
VW3
Computed Breakpoints include

76A3;76B2

Features within 76A3--76B2
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
gamma ray
(Ashburner et al., 1981)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Duffy et al., 1996, Dorer et al., 1995, Harbecke and Lengyel, 1995, Pauli et al., 1995, Ashburner et al., 1981)
Breakpoints

76A3;76B2

(Duffy et al., 1996, Dorer et al., 1995, Harbecke and Lengyel, 1995, Pauli et al., 1995, Ashburner et al., 1981)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

rept << bk1 << M(3)76A << bk2 << Su(Tpl)

Genetic mapping information
Comments
Comments on Cytology

All limits from polytene analysis (FBrf0036112)

Sequence Crossreferences
DDBJ / EMBL / GenBank
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
Completely deleted / disrupted
M(3)76A
(Ashburner et al., 1981)
Partially deleted / disrupted
Molecular Data
Completely deleted
Partially deleted
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

    Complements Df(3L)fln1. Fails to complement Df(3L)kto2.

    (Vigoreaux et al., 1998)
    NOT in combination with other aberrations

    Df(3L)VW3 embryos show defects in tracheal cell migration.

    (Myat et al., 2005)

    Heterozygosity for Df(3L)VW3 results in 0.9% X chromosome nondisjunction and 0.0% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

    (Harris et al., 2003)

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

    (Halsell and Kiehart, 1998)

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

    (Duffy et al., 1996)

    Deficient embryos show a mutant midgut phenotype: visceral mesoderm does not develop.

    (Bilder and Scott, 1995)

    Homozygous embryos do not complete dorsal closure and gastrulation is often abnormal.

    (Harbecke and Lengyel, 1995)

    Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.

    (Pauli et al., 1995)

    Has a Minute phenotype, presumably due to M(3)76A being deleted.

    (Ashburner et al., 1981)

    Minute phenotype

    Stocks (1)
    Notes on Origin
    Discoverer

    Walker.

     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    Df(3L)VW3
    (Crest et al., 2007)
    Df(3L)vw3
    (LaJeunesse et al., 2001)
    VW3
    (Provost et al., 2006, Yamaguchi et al., 2001, Yamaguchi et al., 1999)
    Name Synonyms
    Secondary FlyBase IDs
      References (35)