FB2024_03 , released June 25, 2024
Allele: Dmel\α4GT1EP797
Open Close
General Information
Symbol
Dmel\α4GT1EP797
Species
D. melanogaster
Name
FlyBase ID
FBal0190797
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
EP797
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    Cytology
    Description
    Allele components
    Component
    Use(s)
    Mutations Mapped to the Genome
    Curation Data
    Variant Molecular Consequences
    Associated Sequence Data
    DNA sequence
    Protein sequence
     
    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

    Expression of α4GT1EP797 under the control of Scer\GAL4GMR.PU has no effect on the eye.

    Expression of α4GT1EP797 under the control of Scer\GAL4GMR.PF has no affect on the eye.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    NOT Enhancer of
    Statement
    Reference
    Suppressor of
    NOT Suppressor of
    Statement
    Reference
    Phenotype Manifest In
    NOT Enhancer of
    Statement
    Reference
    Suppressor of
    NOT Suppressor of
    Statement
    Reference
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    Co-expression of α4GT1EP797 has no effect on the small, rough eye phenotype caused by expression of HScer\UAS.cMa under the control of Scer\GAL4GMR.PU.

    Co-expression of α4GT1EP797 suppresses the increased cell death in the developing retina and the adult eye phenotype caused by expression of rprScer\UAS.cUa under the control of Scer\GAL4GMR.PU.

    Co-expression of α4GT1EP797 has no effect on the adult eye phenotype caused by expression of WScer\UAS.cUa under the control of Scer\GAL4GMR.PU.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments

    FlyBase curator comment: In FBrf0190751, α4GT1EP797 was reported to be an enhancer of the eye phenotype caused by expression of HScer\UAS.cMa under the control of Scer\GAL4GMR.PF. However, a subsequent paper (FBrf0215427) shows that this enhancement was due to the snaSco marker allele present on the original α4GT1EP797 chromosome, and that α4GT1EP797 has no effect on the eye phenotype caused by expression of HScer\UAS.cMa under the control of Scer\GAL4GMR.PF.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    α4GT1EP797
    Name Synonyms
    Secondary FlyBase IDs
      References (3)