FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\14-3-3εNP1301
Open Close
General Information
Symbol
Dmel\14-3-3εNP1301
Species
D. melanogaster
Name
FlyBase ID
FBal0223209
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
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)
    Inserted element
    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

    14-3-3εj2B10/14-3-3εNP1301 embryos show highly penetrant axon guidance defects in the ISNb and SNa axons.

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

    The ISNb and SNa axon guidance defects seen in 14-3-3εj2B10/14-3-3εNP1301 embryos are significantly suppressed by expression of either Ras64BVal14.Scer\UAS, ifScer\UAS.cUa or mewScer\UAS.cWa under the control of Scer\GAL414-3-3ε-NP1301.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    The ISNb and SNa axon guidance defects seen in 14-3-3εj2B10/14-3-3εNP1301 embryos are partially suppressed by expression of 14-3-3εScer\UAS.T:Zzzz\FLAG under the control of Scer\GAL414-3-3ε-NP1301.

    Images (0)
    Mutant
    Wild-type
    Stocks (1)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    14-3-3εNP1301
    Name Synonyms
    Secondary FlyBase IDs
      References (2)