FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\capu2F
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General Information
Symbol
Dmel\capu2F
Species
D. melanogaster
Name
FlyBase ID
FBal0045434
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
    Cytology
    Description

    Amino acid replacement: P596T.

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

    C3874354A

    Amino acid change:

    P597T | capu-PA; P587T | capu-PB; P745T | capu-PD; P818T | capu-PE; P899T | capu-PF; P470T | capu-PG; P645T | capu-PH; P836T | capu-PI; P627T | capu-PJ

    Reported amino acid change:
    Comment:

    Site of nucleic acid difference inferred by FlyBase curator based on reported amino acid change; CDS from reference sequence longer by 1 amino acid from published CDS in GB:U34258 and thus the mutation coordinates differ by 1

    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

    The actin mesh (a uniform network of actin filaments present throughout the cytoplasm) that is seen in wild-type stage 9 oocytes is much weaker than normal in mutant oocytes at this stage.

    Less than 5% of embryos laid by homozygous females have abnormal eggshells. Abnormal microtubule distribution in stage 8 and 9 egg chambers (distribution resembles that of stage 10 egg chambers), long and thick tubulin fibres are seen wrapping around the cortex of mutant oocytes. Egg chambers undergo premature microtubule based cytoplasmic streaming.

    External Data
    Interactions
    Show genetic interaction network for Enhancers & Suppressors
    Phenotypic Class
    Phenotype Manifest In
    Enhancer of
    Statement
    Reference

    capu2F is an enhancer of phenotype of chic01320

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    6% of the eggs from capu2/capu2F and 30% from chic01320/chic01320 have fused dorsal appendages, whereas 76% of those from capu2, chic01320/capu2F, chic01320 have dorsal/ventral defects. Similarly capu2F, chic01320/capu2F, chic01320 produce 70% eggs with dorsal/ventral defects while capu2F/capu2F alone produced only 2%.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer
    Comments
    Comments
    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (1)
    Reported As
    Symbol Synonym
    Name Synonyms
    Secondary FlyBase IDs
      References (4)