FB2026_02 , released June 18, 2026
Allele: Dmel\dupa3
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General Information
Symbol
Dmel\dupa3
Species
D. melanogaster
Name
FlyBase ID
FBal0095189
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: ?592term.

    Amino acid replacement: Q592term.

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

    C15377394T

    Amino acid change:

    Q592term | dup-PA; Q592term | dup-PB

    Reported amino acid change:

    Q592term

    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 embryos show weak BrdU incorporation during a prolonged and partial S phase of cycle 16.

    Cells in homozygous dupa1 mutant embryos enter mitosis 16 (M16) later than heterozygous controls. A partial S phase 16 is also seen. Once in M16 the cells are arrested remain in this state until at least stage 13, and mitotic cells are still visible at stage 15. Spindles in these mutants contain apparently functional centrosomes, chromosomes fail to align properly. Most chromosomes lie within the bipolar spindle but are scattered and not compacted into a metaphase plate. Severe alignment defects are seen in about 80% of mitotic cells.

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

    dupa3 has mitotic cell cycle phenotype, suppressible by mei-41D3

    Additional Comments
    Genetic Interactions
    Statement
    Reference

    In dupa3, mei-41D3 double mutants the mitosis 16 (M16) entry delay phenotype is absent. The addition of Bub1k03113 to dupa3 mutants suppresses the M16 arrest phenotype.

    In dupa3, mei-41D3 double mutants the mitosis 16 (M16) entry delay phenotype is absent.

    The addition of BubR1k03113 to dupa3 mutants suppresses the M16 arrest phenotype.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Fails to complement
    Comments
    Images (0)
    Mutant
    Wild-type
    Stocks (1)
    Notes on Origin
    Discoverer
    Comments
    Comments

    dupa3 fails to complement dupl5.

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (6)