FB2024_04 , released June 25, 2024
Allele: Dmel\AbiP2
Open Close
General Information
Symbol
Dmel\AbiP2
Species
D. melanogaster
Name
FlyBase ID
FBal0239155
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Mutagen
    Nature of the Allele
    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

    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.

    9.6% of AbiKO/AbiP2 embryos have midline crossing defects in ipsilateral axon fascicles at stage 17.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Suppressed by
    Statement
    Reference
    Suppressor of
    Statement
    Reference

    Abi[+]/AbiP2 is a suppressor | partially of abnormal neuroanatomy | embryonic stage phenotype of Abl4/Abl1

    Phenotype Manifest In
    Suppressed by
    Statement
    Reference

    AbiP2/AbiKO has larval longitudinal connective phenotype, suppressible | partially by Abl4/Abl[+]

    Suppressor of
    Statement
    Reference

    Abi[+]/AbiP2 is a suppressor | partially of larval longitudinal connective phenotype of Abl4/Abl1

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    The frequency of the midline crossing defect seen in Fas-expressing axons in Abl1/Abl4 embryos is suppressed from 37% to 18% by AbiP2/+.

    The frequency of the midline crossing defect seen in Fas-expressing axons in AbiKO/AbiP2 embryos is suppressed from 9.6% to 3% by Abl4/+.

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

    Precise excision of the insertion reverts the lethal phenotype.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (2)
    Reported As
    Symbol Synonym
    AbiP2
    Name Synonyms
    Secondary FlyBase IDs
      References (1)