FB2026_02 , released June 18, 2026
Allele: Dmel\ord6
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General Information
Symbol
Dmel\ord6
Species
D. melanogaster
Name
FlyBase ID
FBal0032315
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: W294R.

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

T23272774M

Amino acid change:

W294R | ord-PA; W294R | ord-PB

Reported amino acid change:

W294R

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

Recovery of the ring X chromosome R(1)2 relative to a normal rod X chromosome during female meiosis is significantly lowered in ord6/ord10 (ratio of ring/rod=0.4 compared to 0.7 in wild-type) mutants.

Meiotic recombination is reduced but not absent. Females exhibit high levels of sex chromosome missegregation compared to males. Encoded protein is able to poison the activity of ord4 in males and females: negative complementation. Mutation exhibits negative complementation when in combination with ord8 and ord11 in females, missegregation is greater in ord8/ord6 and ord11/ord6 transheterozygotes than that in ord8 or ord11 hemizygotes.

Level of chromosome missegregation in heterozygous males significantly increases when transheterozygous with ord4.

Increased frequency of premature sister chromatid disjunction.

External Data
Interactions
Show genetic interaction network for Enhancers & Suppressors
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

Moderate strength allele.

Does not interact with ord4 to alter the male or female meiotic chromosome segregation phenotype.

Moderate ord mutation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
ord6
Name Synonyms
Secondary FlyBase IDs
    References (5)