FB2024_03 , released June 25, 2024
Allele: Dmel\GSd427GSd427
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General Information
Symbol
Dmel\GSd427GSd427
Species
D. melanogaster
Name
FlyBase ID
FBal0218680
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
GSd427
Key Links
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
    Type
    Location
    Additional Notes
    References
    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 GSd427GSd427 in the developing eye under the control of Scer\GAL4GMR.PF generates a severe defect in R-cell positioning.

    Isolated RP2 neuron clones expressing GSd427GSd427 under the control of Scer\GAL4Act5C.PP (clones generated using the Scer\FLP1eve.RN2 line) show a reduction in dendrite growth and branching at 25-31 hours after egg laying. The distribution of dendrites in the dendritic field is altered: there is a decrease in the number of dendrites targeted to the anterior, posterior, medial and lateral regions of the dendritic field.

    Fas2-positive axon bundles in the ventral nerve cord are missing or disrupted and are diffuse or less distinct than normal in embryos expressing GSd427GSd427 under the control of Scer\GAL4scrt-11-6. In the periphery, the ISNb motor neuron is missing or thinned.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    Suppressed by
    Statement
    Reference
    Additional Comments
    Genetic Interactions
    Statement
    Reference

    A RN-treGSV background completely suppresses the R-cell mislocalization phenotype found upon expression of GSd427GSd427 in the developing eye under the control of Scer\GAL4GMR.PF.

    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 (2)
    Reported As
    Symbol Synonym
    GSd427GSd427
    Name Synonyms
    Secondary FlyBase IDs
      References (4)