FB2026_02 , released June 18, 2026
Allele: Dmel\Gp150k11107b
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General Information
Symbol
Dmel\Gp150k11107b
Species
D. melanogaster
Name
FlyBase ID
FBal0144852
Feature type
allele
Associated gene
Dmel\Gp150
Associated Insertion(s)
Carried in Construct
Also Known As
gp1501
Key Links
Genomic Maps

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

    Contains a 1305bp deletion from exon 5 into exon 6.

    (Li et al., 2003)
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    deletion
    2R:22,327,164..22,328,468 [+]
    Comment:

    A 1305bp deletion from exon 5 into exon 6. The deletion extends from amino acid 620 to 1040 and is followed by a frameshift and translation termination a few residues later.

    (Li et al., 2003)
    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

        When Gp150k11120b/Gp150k11107b clones are made in the eye mutant ommatidia are seen. No specific photoreceptor cell type is found to be mutant at a higher proportion than the others in these clones.

        (Li et al., 2003)

        Mutant adults exhibit a phenotype in the ocellar bristles and sensory organs over the notum. Multiple socket cells are often developed in sensory organs. The external shaft is also often missing or duplicated. Moreover there are cases where both socket and shaft cells are absent in sensory organs.

        (Fetchko et al., 2002)
        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 (0)
        Notes on Origin
        Discoverer

        Separable from: P{lacW}k11107a.

        (FlyBase, 1992-)
        Comments
        Comments

        Mutation is identical to Gp150k11120b.

        (Li et al., 2003)
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (4)
        Reported As
        Symbol Synonym
        Gp150k11107b
        defu1
        (Li et al., 2003)
        gp1501
        (Li et al., 2003, Fetchko et al., 2002)
        l(2)k11107
        (Fetchko et al., 2002)
        Name Synonyms
        Secondary FlyBase IDs
          References (3)