FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\Cks30AHG24
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General Information
Symbol
Dmel\Cks30AHG24
Species
D. melanogaster
Name
FlyBase ID
FBal0014538
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
Cytology
Description

Amino acid replacement: P61S.

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

C9331307T

Amino acid change:

P61S | Cks30A-PA

Reported amino acid change:

P61S

Comment:

Site of nucleic acid difference 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

aster & oocyte

larval cuticle & larval abdomen

larval cuticle & larval abdomen (with Cks30ARA74)

Detailed Description
Statement
Reference

Embryos derived from females homozygous or hemizygous for Cks30AHG24 arrest development at the onset of embryogenesis, typically with a single metaphase mitotic spindle. Some embryos progress through a limited number of divisions before arresting, again in a metaphase-like state. These metaphase-arrested spindles are zygotic and not derived from the female meiotic spindle. In Cks30AHG24 mutants, the first events of female meiosis are unaffected. The karyosome appears normal, and the timing of nuclear envelope breakdown and the appearance of the spindle is also unaffected in the majority of mutant ovaries, although approximately 7% have abnormal spindles and fail chromosome congression on the spindle. Consistent meiotic defects were detected upon ovulation and entry into the second meiotic division. Rotation of the spindle fails in the majority of oocytes, and assembly of the meiosis II spindle is abnormal. The most common defect in Cks30AHG24 mutants is a kink and/or separation of the two tandem spindles. In more severe cases, the meiotic spindle breaks down and chromosome segregation is severely disrupted. Despite these errors, the female meiotic products appear to exit meiosis, reforming nuclear envelopes, and pronuclear fusion occurs. After completion of meiosis, the polar body microtubule aster does not form in Cks30AHG24 mutants, instead a shell of microtubules surrounds the chromatin. Cks30AHG24 and Cks30ARA74/Cks30AHG24 mutants exhibit defects in abdominal cuticle deposition, indicative of a partial disruption of larval abdominal histoblast development.

Embryos derived from homozygous females show embryonic development and form fragmented cuticle.

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

Cks30AHG24/Cks30ARA74 has larval cuticle & larval abdomen phenotype, enhanceable by Cdk1E1-23

Enhancer of
Statement
Reference

Cks30AHG24/Cks30ARA74 is an enhancer of larval cuticle & larval abdomen phenotype of Cdk1E1-23

Additional Comments
Genetic Interactions
Statement
Reference

Cks30ARA74/Cks30AHG24 mutants, in combination with cdc2E1-23 exhibit very strong abdominal cuticle defects.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (0)
Notes on Origin
Discoverer
External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (6)
Reported As
Symbol Synonym
Cks30AHG24
Cks30AHG
rem2
Name Synonyms
Secondary FlyBase IDs
    References (3)