FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Fam92c.4-789Del
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General Information
Symbol
Dmel\Fam92c.4-789Del
Species
D. melanogaster
Name
FlyBase ID
FBal0367233
Feature type
allele
Associated gene
Dmel\Fam92
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Deletion (c.4-789Del) within the endogenous Fam92 locus, removing a large portion of the coding sequence.

    (Wu et al., 2020)
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    deletion
    2L:12,424,941..12,425,886 [+]
    Comment:

    A deletion (c.4-789Del) within Fam92 removes most of the coding sequence.

    (Wu et al., 2020)
    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 ( 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

        Fam92c.4-789Del spermatocytes show elongated primary axonemes (labelled by CG6652).

        (Wu et al., 2020)
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Enhancer of
        Statement
        Reference

        Fam92c.4-789Del is an enhancer of abnormal adult locomotory behavior phenotype of Cep1621

        (Wu et al., 2024)
        Phenotype Manifest In
        Enhanced by
        Statement
        Reference

        Fam92c.4-789Del has axoneme | spermatogenesis phenotype, enhanceable by Rab81

        (Wu et al., 2020)
        Additional Comments
        Genetic Interactions
        Statement
        Reference
        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 (1)
        Reported As
        Symbol Synonym
        Fam92c.4-789Del
        Name Synonyms
        Secondary FlyBase IDs
          References (2)