Amino acid replacement: A424V.
C23272203T
A424V | ord-PA; A424V | ord-PB
A424V
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
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.
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.
FM7a, ord10/ord4 has abnormal meiotic cell cycle phenotype
Weak allele.
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.