FB2026_03 , released September 17, 2026
Allele: Dmel\baboA.ΔI.UAS
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General Information
Symbol
Dmel\baboA.ΔI.UAS
Species
D. melanogaster
Name
FlyBase ID
FBal0155622
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
    Nature of the Allele
    Mutagen
    Progenitor genotype
    Carried in construct
    Cytology
    Description

    UAS sequences regulate expression of a dominant-negative form of the babo a isoform, which retains the ligand-binding domain but lacks the intracellular kinase domain.

    Allele components
    Component
    Use(s)
    Encoded product / tool
    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 baboA.ΔI.Scer\UAS and baboB.ΔI.Scer\UAS together in motorneurons, driven by Scer\GAL4OK6, causes ISNb pathfinding defects and SNa branching defects. The more copies of baboA.ΔI.Scer\UAS that are expressed, the higher the penetrance of the phenotype. This phenotype also occurs when baboA.ΔI.Scer\UAS is expressed under the control of Scer\GAL4elav-C155.

    Expression of baboA.ΔI.Scer\UAS and baboB.ΔI.Scer\UAS together in muscle, driven by Scer\GAL4Mef2.PR, results in a low penetrance of weak ISNb defects and no SNa defects.

    When baboA.ΔI.Scer\UAS and baboB.ΔI.Scer\UAS are expressed together in glia, under the control of Scer\GAL4repo, only 4% of hemisegments show ISNb pathfinding defects and 2% show SNa branching defects.

    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 (1)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    baboA.ΔI.Scer\UAS
    baboA.ΔI.UAS
    Name Synonyms
    Secondary FlyBase IDs
      References (2)