FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\wfs1LL07290
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General Information
Symbol
Dmel\wfs1LL07290
Species
D. melanogaster
Name
FlyBase ID
FBal0344129
Feature type
allele
Associated gene
Dmel\wfs1
Associated Insertion(s)
PBac{SAstopDsRed}wfs1LL07290
Carried in Construct
Key Links
Genomic Maps

Allele class

hypomorphic allele - molecular evidence

Mutagen
    Nature of the Allele
    Allele class

    hypomorphic allele - molecular evidence

    (Sakakibara et al., 2018)
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    PBac{SAstopDsRed}wfs1LL07290
    Cytology
    Description
    Allele components
    Component
    Use(s)
    Inserted element
    PBac{SAstopDsRed}
    Mutations Mapped to the Genome
    Curation Data
    Variant Molecular Consequences
    Associated Sequence Data
    DDBJ / EMBL / GenBank
    DNA sequence
    Protein sequence
     
    UniProtKB/Swiss-Prot
      UniProtKB/TrEMBL
        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 ( 1 )
        Disease
        Evidence
        References
        model of  Wolfram syndrome 1
        CEC
        (Sakakibara et al., 2018)
        Modifiers Based on Experimental Evidence ( 0 )
        Disease
        Interaction
        References
        Comments on Models/Modifiers Based on Experimental Evidence ( 1 )
         

        FlyBase curator comment: "Wolfram syndrome 1" is associated with human ortholog WFS1.

        (Sakakibara et al., 2018)
        Disease-implicated variant(s)
         
        Phenotypic Data
        Phenotypic Class
        Phenotype Manifest In
        Detailed Description
        Statement
        Reference

        wfs1LL07290 homozygous and heterozygous adults show age-dependent climbing defects compared to controls, which are more severe in homozygotes. Homozygotes also show a severely impaired righting reflex.

        (Sakakibara et al., 2018)
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Phenotype Manifest In
        Additional Comments
        Genetic Interactions
        Statement
        Reference
        Xenogenetic Interactions
        Statement
        Reference
        Complementation and Rescue Data
        Comments
        Images (0)
        Mutant
        Wild-type
        Stocks (1)
        Notes on Origin
        Discoverer
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (1)
        Reported As
        Symbol Synonym
        wfs1LL07290
        (Sakakibara et al., 2018)
        Name Synonyms
        Secondary FlyBase IDs
          References (1)