FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\cmetΔ
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General Information
Symbol
Dmel\cmetΔ
Species
D. melanogaster
Name
FlyBase ID
FBal0118293
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description

Imprecise excision of the P{PZ} element deleting approximately 5kb of genomic DNA just upstream of the 5' end of the initial P{PZ} element insertion site.

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

Spermatids from mutant third instar larvae testes do not show cytokinesis defects.

Mutant spermatocytes form meiotic spindles with centrosomes at the poles that are indistinguishable from wild-type spindles.

Homozygous spermatocytes often show unequal DNA segregation in meiosis I.

The brains of homozygous cmetΔ larvae contain aneuploid cells and precocious sister chromatid separation.

The fraction of mitotic cells in larval brain squashes is increased compared to wild type. There is an increase in the number of prometaphase/metaphase figures. The mitotic cells frequently contain misaligned chromosomes. Chromosomes sometimes appear to be undercondensed. Embryos derived from homozygous female germline clones are produced at low frequencies. 20% of the embryos show defects, such as an unusual overall shape, that are strongly suggestive of abnormal oogenesis. In the few embryos obtained, prominent chromosome alignment defects are seen and well as many nuclei with abnormally high chromosome content. Maintenance of chromosome congression is clearly aberrant; tight metaphase alignment of most chromosomes is not maintained and the misaligned chromosomes may stay misaligned through initiation of anaphase. Both sister chromatids may migrate to the same pole. Anaphase duration is not detectably extended.

External Data
Interactions
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Phenotypic Class
Phenotype Manifest In
Additional Comments
Genetic Interactions
Statement
Reference
Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (1)
Notes on Origin
Discoverer
Comments
Comments
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (2)
Reported As
Name Synonyms
Secondary FlyBase IDs
    References (5)