FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Cenp-CIR35
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General Information
Symbol
Dmel\Cenp-CIR35
Species
D. melanogaster
Name
FlyBase ID
FBal0190490
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: Q858term.

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

    C8567022T

    Amino acid change:

    Q858term | Cenp-C-PA; Q846term | Cenp-C-PB

    Reported amino acid change:

    Q858term

    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

    Cenp-CZ3-4375/Cenp-CIR35 females show defects in centromere clustering in the oocyte, with a failure of clustering being evidence by pachytene in region 3 of the germarium (centromere clustering at the earlier zygotene stage is normal). Defects in centromere pairing are also seen.

    The centromeres are separated from the nucleolus in the oocytes of Cenp-CZ3-4375/Cenp-CIR35 females (in contrast to wild type where they are adjacent).

    Heterozygous females show significantly increased X chromosome nondisjunction compared to wild-type controls. The nondisjunction events occur in meiosis I.

    Mutants show cell cycle defects during embryogenesis.

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

    Cenp-CIR35/Df(3R)Exel6176 double heterozygous females do not show a significant increase in X chromosome non disjunction compared to wild-type controls.

    cal12k32/Cenp-CIR35 and Df(3R)Exel6176/Cenp-CIR35 double heterozygous females show defects in centromere clustering in the oocyte, with defects being evident by region 3 of the germarium. Defects in centromere pairing are also seen.

    The centromeres are separated from the nucleolus in the oocytes of double heterozygous cal12k32/Cenp-CIR35 females (in contrast to wild type where they are adjacent).

    cal12k32/Cenp-CIR35 double heterozygous females show significantly increased X and 4th chromosome nondisjunction compared to wild-type controls, with the frequency of nondisjunction being increased compared to the phenotypes seen in single heterozygotes.

    Xenogenetic Interactions
    Statement
    Reference
    Complementation and Rescue Data
    Comments

    Cenp-CT:Avic\GFP-EYFP restores normal centromere clustering in the oocytes of Cenp-CZ3-4375/Cenp-CIR35 females.

    Images (0)
    Mutant
    Wild-type
    Stocks (0)
    Notes on Origin
    Discoverer

    K. Dej T. Orr-Weaver

    External Crossreferences and Linkouts ( 0 )
    Synonyms and Secondary IDs (3)
    Reported As
    Name Synonyms
    Secondary FlyBase IDs
      References (5)