Nucleotide substitution: C?T.
Amino acid replacement: Q267term.
C16774618T
C?T
Q267term | Nrt-PA; Q267term | Nrt-PB; Q267term | Nrt-PC
Q267term
Induced on: Df(3L)st-j7. The NrtM29 mutant allele was originally thought to be a mutation in the Dab gene (see FBrf0049327, FBrf0058531 and FBrf0084025), but sequencing of the chromosome indicates that it is a lesion in the Nrt gene.
Induced on: Df(3L)st-j7.
Complements: l(3)73Bcunspecified.
Haploinsufficiency dependent upon an Abl mutant background (HDA).