FB2025_01 , released February 20, 2025
Allele: Dmel\dyscc05107
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General Information
Symbol
Dmel\dyscc05107
Species
D. melanogaster
Name
FlyBase ID
FBal0225094
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
CG34400c05107
Key Links
Genomic Maps

Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    Cytology
    Description

    Expression of all dysc isoforms is reduced but still detectable in dyscc05107 mutants.

    Allele components
    Component
    Use(s)
    Mutations Mapped to the Genome
    Curation Data
    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

    dyscc05107 homozygotes display relatively mild arrhythmic locomotor patterns in constant dark conditions, with some animals showing robust rhythmicity.

    In 12 h light:dark conditions, anticipation of both lights-on and lights-off is maintained in dyscc05107 flies. Overall daytime and nighttime activity is greater in these mutants compared to wild type in these conditions.

    dyscs168/dyscc05107 animals display arrhythmic locomotor patterns in constant dark conditions.

    dyscc03838/dyscc05107 animals display arrhythmic locomotor patterns in constant dark conditions.

    dyscc07121/dyscc05107 mutant flies show significant indirect flight muscle degeneration compared to controls.

    dyscc05107/+ mutant flies do not exhibit temperature-induced mobility defects.

    dyscc05107 mutant third instar larvae display a significantly increased frequency of axon migration abnormalities in the brain compared to controls, resulting in defects in the lamina plexus.

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

    Combination of Df(3R)Exel6184 in heterozygous state with a single copy of dyscc05107 results in a significantly increased frequency of lamina plexus defects in the third instar larval brain in the double heterozygotes.

    Combination of DgO86 in heterozygous state with a single copy of dyscc05107, results in significantly increased frequency of lamina plexus defects in third instar larvae.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Symbol Synonym
    CG43749c05107
    Name Synonyms
    Secondary FlyBase IDs
      References (4)