FB2025_01 , released February 20, 2025
Allele: Dmel\αTub67C1
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General Information
Symbol
Dmel\αTub67C1
Species
D. melanogaster
Name
FlyBase ID
FBal0000008
Feature type
allele
Associated gene
Associated Insertion(s)
Carried in Construct
Key Links
Nature of the Allele
Progenitor genotype
Cytology
Description
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

αTub67C1/αTub67C2 females show severe defects in bipolar spindle formation in the oocyte.

X/FM7a; αTub67C1/+ females show elevated levels of X chromosome nondisjunction.

Eggs derived from females transheterozygous for αTub67Cunspecified and αTub67C1 have abnormal gonomeric spindles. Abnormal ectopic cleavage spindles form, the abnormality becoming more severe with time.

αTub67C3/αTub67C1 females produce patroclinous daughters at low frequency; these females arise by fusion of haploid cleavage nuclei or failure of newly replicated haploid chromosomes to segregate.

No eggs from hemizygous females hatch. Many are apparently unfertilized, though insemination occurs. Paternal genotype has no effect on viability of progeny. Majority of eggs had 3 or fewer nuclei. This allele also shows a dominant reduction in female fertility.

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

αTub67C1 has phenotype, enhanceable by ncdD

Suppressed by
Statement
Reference

αTub67C1 has phenotype, suppressible by nodunspecified

Enhancer of
Statement
Reference

αTub67C1 is an enhancer of phenotype of ncdD

Additional Comments
Genetic Interactions
Statement
Reference

Does not interact with alleles of sub.

ncdD/ncdD enhances the production of exceptional androgenetic females by αTub67C1 heterozygotes. αTub67C1 dominantly enhances the frequencies of nondisjunction and zygotic loss of the X chromosome in ncdD/ncdD flies.

Xenogenetic Interactions
Statement
Reference
Complementation and Rescue Data
Images (0)
Mutant
Wild-type
Stocks (2)
Notes on Origin
Discoverer

K. Matthews.

Comments
Comments

Based on average degree of development of eggs of the hemizygous mutant genotype the alleles can be ranked, from most to least severe, in the order αTub67C2 < αTub67C4 < αTub67C1 < αTub67C3. Based on the semidominant phenotypes the rank order is αTub67C3 < αTub67C1 = αTub67C2 = αTub67C4.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (4)
References (16)