FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\mad2Δ
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General Information
Symbol
Dmel\mad2Δ
Species
D. melanogaster
Name
FlyBase ID
FBal0247990
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Genomic Maps

Allele class
Nature of the Allele
Allele class
Progenitor genotype
Caused by aberration
Cytology
Description

Generated through imprecise excision of P{PZ}S6k07084 resulting in Df(3)07084 with a deletion of 3150bp, removing the last 180bp of mad2, all of gene CG5537 and the first 1120bp of S6k.

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

Deletion resulting from imprecise excision of P{PZ}S6k07084. Location deduced from description of mad2Delta as a deletion of 3150 base pairs, removing the last 180 base pairs of mad2, all of kri, and the first 1120 base pairs of S6k. Deletion mapped from breakpoint in mad2.

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 ( 1 )
Disease
Evidence
References
Modifiers Based on Experimental Evidence ( 1 )
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

mad2Δ dividing cells in third instar larval brains rarely exhibit aneuploidy and do not show any increase in apoptosis. However, the aneuploid cells are qualitatively different from those of wild-type, with almost all being polyploids, suggesting a rare complete failure of segregation.

mad2Δ mutants do not show accumulation of mitotic cells in colchicine-treated larval brains.

There are no obvious aberrations in chromosome behaviour in mad2Δ mutants compared to controls. Mitosis appears to function normally in mad2Δ cells although anaphase onset is accelerated in mad2Δ mutant neuroblasts. The time from nuclear envelope breakdown to the onset of CycB degradation is substantially reduced in mad2Δ mutants. The average time required to degrade spindle-associated CycB and initiate anaphase in mad2Δ cells is longer than the average time for achieving alignment of kinetochores on the metaphase place.

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

mad2Δ mutants suppress the high mitotic index seen in aspE3 brains.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Comments
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (2)