Amino acid replacement: Q930term.
C17091249T
Q931term | cal1-PA
Q930term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Heterozygous females show significantly increased X and 4th chromosome nondisjunction compared to wild-type controls. The nondisjunction events occur in meiosis I.
Isolated cells in the central nervous system have increased nuclear size and ploidy in homozygous embryos.
cal12k32 has abnormal meiotic cell cycle | semidominant phenotype, enhanceable by Cenp-C[+]/Cenp-CIR35
cal12k32/cal1[+] is an enhancer of abnormal meiotic cell cycle | semidominant phenotype of Cenp-CIR35
Cenp-CIR35, cal12k32/cal1[+] has chromosome, centromeric region phenotype
Cenp-C[+]/Cenp-CIR35, cal12k32 has oocyte phenotype
Cenp-C[+]/Cenp-CIR35, cal12k32 has chromosome, centromeric region phenotype
Df(3R)Exel6149/+, cal12k32 has oocyte phenotype
Df(3R)Exel6149/+, cal12k32 has chromosome, centromeric region phenotype
Cenp-C[+]/Cenp-CZ3-4375, cal12k32 has oocyte phenotype
Cenp-C[+]/Cenp-CZ3-4375, cal12k32 has chromosome, centromeric region phenotype
cal12k32/Df(3R)Exel6149 double heterozygous females do not show a significant increase in X chromosome non disjunction compared to wild-type controls.
cal12k32/Cenp-CIR35, cal12k32/Df(3R)Exel6149 and cal12k32/Cenp-CZ3-4375 double heterozygous females show defects in centromere clustering in the oocyte, with defects being evident by region 3 of the germarium. Defects in centromere pairing are also seen.
The centromeres are separated from the nucleolus in the oocytes of double heterozygous cal12k32/Cenp-CIR35 females (in contrast to wild type where they are adjacent).
cal12k32/Cenp-CIR35 double heterozygous females show significantly increased X and 4th chromosome nondisjunction compared to wild-type controls, with the frequency of nondisjunction being increased compared to the phenotypes seen in single heterozygotes.