FB2024_04 , released June 25, 2024
Allele: Dmel\AbiP1
Open Close
General Information
Symbol
Dmel\AbiP1
Species
D. melanogaster
Name
FlyBase ID
FBal0239154
Feature type
allele
Associated gene
Dmel\Abi
Associated Insertion(s)
P{EP}AbiP1
Carried in Construct
Key Links
Allele class

hypomorphic allele - genetic evidence

Mutagen
    Nature of the Allele
    Allele class

    hypomorphic allele - genetic evidence

    (Lin et al., 2009)
    Mutagen
    Progenitor genotype
    Associated Insertion(s)
    P{EP}AbiP1
    Cytology
    Description
    Allele components
    Component
    Use(s)
    Inserted element
    P{EP}
    Regulatory region(s)
    UAS
    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

        More than 60% of AbiP1/Df(3R)JY19 and AbiP1/AbiKO animals survive to adulthood.

        Embryos maternally hypomorphic for Abi function and lacking zygotic Abi function (derived from AbiP1/Df(3R)JY19 females mated to AbiP2 carrying males) have deranged longitudinal connectives and commissural tracts. 57.1% of these embryos have midline crossing defects in ipsilateral axon fascicles at stage 17.

        (Lin et al., 2009)
        External Data
        Interactions
        Show genetic interaction network for Enhancers & Suppressors
        Phenotypic Class
        Suppressor of
        Statement
        Reference

        Abi[+]/AbiP1 is a suppressor | partially of lethal phenotype of Abl4/Abl1

        (Lin et al., 2009)
        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
        External Crossreferences and Linkouts ( 0 )
        Synonyms and Secondary IDs (2)
        Reported As
        Symbol Synonym
        AbiP1
        abiP1
        (Lin et al., 2009)
        Name Synonyms
        Secondary FlyBase IDs
          References (1)