Amino acid replacement: S221L. S221 falls in the putative ATP binding domain.
C20076518T
S221L | neb-PA
S221L
Mutant embryos derived from germline clones have holes in cuticle, are missing abdominal segments and have head involution defects. Germline clone females have 1-5% fourth chromosome non-disjunction. Escapers have many missing bristles, behavioural defects and wings held out perpendicular to the body.
nebTE12 has abnormal meiotic cell cycle phenotype, enhanceable by nod[+]/nod2
nebTE12 has abnormal meiotic cell cycle phenotype, enhanceable by nod[+]/nod3
nebTE12 has abnormal meiotic cell cycle phenotype, enhanceable by nod[+]/nod4
neb[+]/nebTE12 is an enhancer of abnormal meiotic cell cycle phenotype of nod2
neb[+]/nebTE12 is an enhancer of abnormal meiotic cell cycle phenotype of nod4
neb[+]/nebTE12 is an enhancer of abnormal meiotic cell cycle phenotype of nod3
nebTE12, nodDTW has female sterile | dominant phenotype
nebTE12 is a suppressor of phenotype of kniunspecified
Weak allele.