FB2020_06, released Dec 22, 2020

Aberration: Dmel\Df(3R)Dfd13

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General Information
Symbol
Df(3R)Dfd13
Species
D. melanogaster
Name
Deficiency (3R) Deformed
FlyBase ID
FBab0002523
Feature type
chromosomal_deletion
Computed Breakpoints include

83E3;84B1

Features within 83E3--84B1
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Dfd1
(Hazelrigg and Kaufman, 1983)
Mutagen
X ray
(Pattatucci et al., 1991, Hazelrigg and Kaufman, 1983)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Pauli et al., 1995, Pattatucci et al., 1991, Hazelrigg and Kaufman, 1983)
Breakpoints

83E3;84A4-84A5

(Pauli et al., 1995, Pattatucci et al., 1991, Hazelrigg and Kaufman, 1983)
Causes alleles
Dfdrv2
ScrDfd13
(Southworth and Kennison, 2002)
Carries alleles
Transposon Insertions
Formalized genetic data

Tpl << bk1 << twr << ftz << bk2 << Antp

Genetic mapping information
Comments
Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0039462) Left limit of break 2 from inclusion of Scr (FBrf0039462) Right limit of break 2 from non-inclusion of Antp (FBrf0039462)

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

    The Df(3R)Dfd13 chromosome acts as a dominant moderate 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)

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

    (Pauli et al., 1995)

    Reduced-sex-comb phenotype in heterozygotes.

    Stocks (2)
    Notes on Origin
    Discoverer

    Hazelrigg.

     

    Revertant

    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (6)
    Reported As
    Symbol Synonym
    Df(3R)Dfd-+Rx13
    Df(3R)Dfd13
    Df(3R)Dfd+RX13
    (Hazelrigg and Kaufman, 1983)
    Dfd+Rx13
    (Pattatucci et al., 1991)
    RX13
    (Kaufman et al., 1990)
    Name Synonyms
    Deficiency (3R) Deformed
    Secondary FlyBase IDs
      References (14)