FB2026_02 , released June 18, 2026
Allele: Dmel\Or67dZ5499
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General Information
Symbol
Dmel\Or67dZ5499
Species
D. melanogaster
Name
FlyBase ID
FBal0240755
Feature type
allele
Associated gene
Dmel\Or67d
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

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

    Amino acid replacement: C23W.

    (Jin et al., 2008)

    The single amino acid substitution, near the N-terminus, is predicted to be intracellular, so this mutation could disrupt the structural integrity of the receptor or its ability to activate downstream components.

    (Jin et al., 2008)
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    point_mutation
    3L:10,273,272..10,273,272 [+]
    Nucleotide change:

    C10273272G

    Amino acid change:

    C23W | Or67d-PA

    Reported amino acid change:

    C23W

    Comment:

    Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

    (Jin et al., 2008)
    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

        Or67dZ5499 mutants are defective for cVA (11-cis-vaccenyl acetate) sensitivity but also have striking defects in most olfactory responses.

        (Jin et al., 2008)
        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
        Fails to complement

        Or67dGAL4-2

        (Jin et al., 2008)
        Comments
        Images (0)
        Mutant
        Wild-type
        Stocks (0)
        Notes on Origin
        Discoverer
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (2)
        Reported As
        Symbol Synonym
        Or67dZ5499
        (Jin et al., 2008)
        vainC1
        (Jin et al., 2008)
        Name Synonyms
        Secondary FlyBase IDs
          References (1)