FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Syx1ASH0113
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General Information
Symbol
Dmel\Syx1ASH0113
Species
D. melanogaster
Name
FlyBase ID
FBal0348117
Feature type
allele
Associated gene
Dmel\Syx1A
Associated Insertion(s)
Carried in Construct
Key Links
Allele class

hypomorphic allele - molecular evidence

Mutagen
    Nature of the Allele
    Allele class

    hypomorphic allele - molecular evidence

    (Tian et al., 2013)
    Mutagen
    Progenitor genotype
    Cytology
    Description

    No sequence changes have been identified within the Syx1A open reading frame.

    (Tian et al., 2013)
    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    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
        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

        Complementation, rescue and P-element excision analysis demonstrates that the homozygous lethality of the 'SH0113' chromosome, plus the grk protein mislocalization defects seen in homozygous 'SH0113' germ-line clones, are not due to the P{lacW}SH0113 insertion (which is inserted near the wake gene), but are instead due to a second-site mutation that affects the Syx1A gene (this mutation is represented by the Syx1ASH0113 allele).

        (Tian et al., 2013)
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (2)
        Reported As
        Symbol Synonym
        Syx1ASH0113
        (Tian et al., 2013)
        syxSH113
        (Tian et al., 2013)
        Name Synonyms
        Secondary FlyBase IDs
          References (1)