FB2021_01, released Feb 18, 2021

Aberration: Dmel\Df(3L)R-G5

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General Information
Symbol
Df(3L)R-G5
Species
D. melanogaster
Name
Deficiency (3L) Roughened
FlyBase ID
FBab0002346
Feature type
chromosomal_deletion
Also Known As
Df(3L)RG5
Computed Breakpoints include

62A10-62B1;62C4-62D1

Features within 62A10--62D4
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Rap11
(Sliter et al., 1989)
Mutagen
gamma ray
(Sliter et al., 1989)
Class of aberration (relative to wild type)
chromosomal_deletion
(FlyBase, 2007)
Class of aberration (relative to progenitor)
chromosomal_deletion
(Coyne, 1996, Pauli et al., 1995, Mason, 19??)
Breakpoints

62A10-62B1;62C4-62D1

(Coyne, 1996, Sliter et al., 1989, Mason, 19??)

62A10-62A13;63C3-63C5

(Pauli et al., 1995)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << l(3)Lak << sls << bk2 << ecd

Genetic mapping information
Comments

This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).

(Marygold et al., 2007)
Comments on Cytology

Ref: Sliter et al., 1989, Genetics 123: 327--336

(Cripps et al., 1994)

All limits from polytene analysis (FBrf0049893)

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

    Flies heterozygous for the deletion do not show a Minute bristle phenotype.

    (Marygold et al., 2007)

    The Df(3L)R-G5 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)

    Does not cause unconditional lethality in hybrid females when heterozygous with D.simulans chromosome.

    (Coyne et al., 1998)

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

    (Halsell and Kiehart, 1998)

    Deficient embryos show an uninterpretable mutant midgut phenotype.

    (Bilder and Scott, 1995)

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

    (Pauli et al., 1995)

    Heterozygotes with In(3LR)TM3 display abnormal indirect flight muscle (IFM) myofibrils, frequent aberrations in Z-disc shape and Z-discs that do not span the myofibril. Transverse sections of muscles show the periphery of the thick and thin filament lattice is disorganised.

    (Cripps et al., 1994)
    Stocks (3)
    Notes on Origin
    Discoverer

    J. Bonner.

    T. Sliter.

    (Mason, 19??)
     

    Revertant

    (Sliter et al., 1989)
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Used in D.melanogaster/D.simulans hybrids to map at least four non-overlapping regions on the D.simulans 3R that have effects on the species difference of cuticular hydrocarbon profile.

    (Coyne, 1996)
    Synonyms and Secondary IDs (4)
    Reported As
    Symbol Synonym
    Df(3L)R-G5
    (Crest et al., 2007)
    Df(3L)RG5
    (Brumby et al., 2004, Zhang et al., 2000, Bhat et al., 1999, Cripps et al., 1994, Cutforth and Rubin, 1994, Sliter et al., 1989, Mason, 19??)
    Df(3L)RG5
    (Pauli et al., 1995)
    Name Synonyms
    Deficiency (3L) Roughened
    Secondary FlyBase IDs
      References (29)