FB2024_03 , released June 25, 2024
Allele: Dmel\PscvgD
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General Information
Symbol
Dmel\PscvgD
Species
D. melanogaster
Name
FlyBase ID
FBal0045021
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
Pscvg-D
Key Links
Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Caused by aberration
    Cytology
    Description

    Distal break of Df(2R)vg-D falls in the Psc transcription unit.

    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Variant Molecular Consequences
    Associated Sequence Data
    DNA sequence
    Protein sequence
     
    Expression Data
    Reporter Expression
    Additional Information
    Statement
    Reference
     
    Marker for
    Reflects expression of
    Reporter construct used in assay
    Human Disease Associations
    Disease Ontology (DO) Annotations
    Models Based on Experimental Evidence ( 0 )
    Disease
    Evidence
    References
    Modifiers Based on Experimental Evidence ( 0 )
    Disease
    Interaction
    References
    Comments on Models/Modifiers Based on Experimental Evidence ( 0 )
     
    Disease-implicated variant(s)
     
    Phenotypic Data
    Phenotypic Class
    Phenotype Manifest In
    Detailed Description
    Statement
    Reference

    Heterozygous males do not have ectopic sex combs on the second and third legs.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Flies doubly heterozygous for PscvgD and Su(z)2vgD show a slight increase in double strand break (DSB) repair via homologous recombination and a corresponding decrease in DSB repair by nonhomologous end-joining compared to controls in a somatic DSB repair assay, when either whd80k17 or whd-y+ is used as the recipient allele bearing the target break site.

    rept06945 shows little or no interaction (in terms of ectopic sex comb phenotype) when in double heterozygous combination with PscvgD.

    No significant modification of the number of sex combs is seen in PscvgD/+ corto420/+ double heterozygotes compared to PscvgD/+ single heterozygotes.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (2)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (5)