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General Information
Symbol
Df(3R)red1
Species
D. melanogaster
Name
Deficiency (3R) red Malpighian tubules
FlyBase ID
FBab0002877
Feature type
Also Known As
Df(3R)red1
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Mutagen
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

bk1 << cash << bk2 << put

Genetic mapping information
Comments
Comments on Cytology

Right limit of break 1 from inclusion of ems (FBrf0049810) Left limit of break 2 from inclusion of l(3)06951 (FBrf0067338) Right limit of break 2 from non-inclusion of l(3)03719 (FBrf0067338)

Sequence Crossreferences
DNA sequence
Protein sequence
Gene Deletion and Duplication Data
Genes Deleted / Disrupted
Complementation Data
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
    NOT in combination with other aberrations

    Homozygotes for Df(3R)red1 fail to hatch.

    The Df(3R)red1 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).

    Heterozygosity for Df(3R)red1 results in 1.6% X chromosome nondisjunction and 0.6% fourth chromosome nondisjunction in In(1)FM7/X ; svspa-pol females.

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

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

    Midgut development of mutant embryos is wild type.

    Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2.

    Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980).

    Stocks (2)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     
    Synonyms and Secondary IDs (4)
    Reported As
    Name Synonyms
    Deficiency (3R) red Malpighian tubules
    Secondary FlyBase IDs
      References (28)