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General Information
Symbol
Df(3R)p13
Species
D. melanogaster
Name
Deficiency (3R) pink
FlyBase ID
FBab0002853
Feature type
Also Known As
Df(3R)p13
Computed Breakpoints include
Sequence coordinates
Member of large scale dataset(s)
Nature of Aberration
Cytological Order
Progenitor
Class of aberration (relative to wild type)
Causes alleles
Carries alleles
Transposon Insertions
Formalized genetic data

l(3)84Ef << bk1 << grn << hb << bk2 << pyd

Genetic mapping information
Comments

This deletion removes multiple ribosomal protein-coding genes (in addition to other genes).

Distal breakpoint of Df(3R)p13 molecularly mapped to the DNA (Tautz et al., 1987)

Comments on Cytology

Limits of break 1 from polytene analysis (FBrf0054129) Left limit of break 2 from inclusion of hb (FBrf0047064) Right limit of break 2 from non-inclusion of pyd (FBrf0089614)

Sequence Crossreferences
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

    Df(3R)p13 flies show no dominant effect on adult eye morphology at either 18[o] or 29[o]C.

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

    The Df(3R)p13 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).

    Suppresses the ommatidial polarity phenotype of dshhs.sev.B. Suppresses the ommatidial polarity phenotype of msnEP549 when driven by Scer\GAL4hs.2sev.

    No interaction with P{sev-svp1} or P{sev-svp2} exists.

    Df(3R)p13/Df(3R)dsx29 heterozygotes lack all ventral chordotonal organs and usually all scolopodia of lch5. External sense organs are essentially unaffected.

    Males fertile when in combination with αTub84B7.

    Homozygotes exhibit an hb- phenotype.

    Stocks (3)
    Notes on Origin
    Discoverer
     
    Balancer / Genotype Variants of the Aberration
     
    Separable Components
     
    Other Comments
     

    Distal breakpoint is at position +64kb of the molecular map of the hb domain.

    Synonyms and Secondary IDs (9)
    References (55)