FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
Allele: Dmel\ord4
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General Information
Symbol
Dmel\ord4
Species
D. melanogaster
Name
FlyBase ID
FBal0032313
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: A424V.

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

C23272203T

Amino acid change:

A424V | ord-PA; A424V | ord-PB

Reported amino acid change:

A424V

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

When ord4/ord10 female flies with normal X chromosomes are subjected to a 4-day aging regimen (after collection of virgin females and feeding with yeast paste overnight, the virgin females are kept for 4 days in the absence of males, which results in the majority of oocytes halting in developmental progression and aging within the female abdomen, as oviposition is suppressed), sex chromosome nondisjunction is not significantly greater in aged oocytes than in non-aged oocytes.

Meiotic crossovers on the X chromosomes are substantially reduced in ord4/ord10 oocytes; the total map distance is reduced to 20% or less of the wild type value.

When subjected to the aging regimen, FM7a/X ; ord4/ord10 aged oocytes show a significant increase in nondisjunction that lasted for 48 hours. Reductional nondisjunction events predominate in both aged and non-aged oocytes.

When subjected to the aging regimen, Df(1)bb158/X ; ord4/ord10 females show age-dependent nondisjunction; sex chromosome nondisjunction is significantly greater in aged oocytes than in non-aged oocytes.

When subjected to the aging regimen, In(1)dl-49/X ; ord4/ord10 females do not show age-dependent nondisjunction.

Heterochromatin pairing between the FM7a chromosome and a normal X chromosome is significantly disrupted in ord4/ord10 oocytes.

ord4/Df(2R)3-70 mothers do not exhibit a significant age dependant increase in meiotic non-disjunction.

Females exhibit high levels of sex chromosome missegregation compared to males. Mutation exhibits negative complementation when in combination with ord1, ord2 or ord6 in males and females, protein activity is poisoned.

Levels of chromosome missegregation in homozygous males and females is very low. Female levels increase only slightly when transheterozygous with Df(2R)3-70, but are significant when transheterozygous with ord1 or ord2. Male levels do not increase when transheterozygous with Df(2R)3-70 or ord2, but are significant when transheterozygous with ord1.

Increased frequency of premature sister chromatid disjunction.

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

ord4/ord10 animals also carrying FM7a balancer an age dependant increase in meiotic non-disjunction is seen.

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

ord1 and ord2 interact with ord4 to alter the female meiotic chromosome segregation phenotype but ord3, ord5 and ord6 do not. ord1 and ord6 interacts with ord4 to alter the male meiotic chromosome segregation phenotype, the remaining alleles do not.

Moderate ord mutation.

External Crossreferences and Linkouts ( 0 )
Synonyms and Secondary IDs (1)
Reported As
Symbol Synonym
Name Synonyms
Secondary FlyBase IDs
    References (6)