FB2026_02 , released June 18, 2026
Allele: Dmel\Ofut14R6
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General Information
Symbol
Dmel\Ofut14R6
Species
D. melanogaster
Name
FlyBase ID
FBal0152355
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Also Known As
o-fut14R6
Key Links
Genomic Maps

Allele class
Mutagen
    Nature of the Allele
    Allele class
    Mutagen
    Progenitor genotype
    Cytology
    Description

    Amino acid replacement: K133term.

    Mutations Mapped to the Genome
    Curation Data
    Type
    Location
    Additional Notes
    References
    Nucleotide change:

    A14161914T

    Amino acid change:

    K133term | O-fut1-PA; K133term | O-fut1-PB

    Reported amino acid change:

    K133term

    Comment:

    Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.

    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

    Homozygous O-fut14R6 clones in the adult intestine which also express O-fut1R245A.Scer\UAS under the control of Scer\GAL4tub.PU show an increase in intestinal stem cell-like cells compared to wild type, without affecting the specification or differentiation of enteroendocrine cells or large enterocytes.

    Embryos maternally and zygotically mutant for O-fut14R6 (generated using females carrying homozygous O-fut14R6 germline clones) exhibit a neurogenic phenotype, in which excess neurons are produced at the expense of epidermal cells.

    Embryos expressing O-fut1R245A in a maternal and zygotic O-fut14R6 mutant background exhibit normal neurogenesis. The embryos are able to hatch, but die as first instar larvae.

    O-fut14R6 homozygous embryos are normal with respect to neurogenesis, but embryos derived from O-fut14R6 homozygous germ-line clones show a strong neurogenic phenotype that is not significantly paternally rescued. In the adult wing, O-fut14R6 mutant clones result in loss of wing margin and vein thickening.

    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
    Partially rescued by

    Ofut14R6 is partially rescued by Ofut1hs.PS

    Comments

    Expression of O-fut1R245A rescues the neurogenic defects seen in embryos that are maternally and zygotically mutant for O-fut14R6.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (4)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (10)