FlyBase curator comment: this entry is used to capture phenotypic information when the particular allele (or allele combination) used by the author could not be determined but the context of the experiment suggests that the phenotype being described is some kind of loss of function.
Sxlf1, msl-1unspecified has abnormal sex-determination | dominant | female phenotype
Sxlf1, msl-1unspecified has visible | dominant | female phenotype
Sxlf1, msl-1unspecified has abnormal sex-determination | female phenotype
Sxlf1, msl-1unspecified has visible | female phenotype
Sxlf1, msl-1unspecified has prothoracic metatarsus | female phenotype
msl-1unspecified/+ partly suppresses the increase in eye pigmentation seen in ocmL714X/+ males homozygous for the P{GMroX1}75C insertion.
Some females homozygous for msl-1unspecified and heterozygous for Sxlf1 have sex combs on the basitarsi of their forelegs. This phenotype occurs with a higher frequency in females with homozygous msl-1unspecified mothers.
msl-1unspecified is rescued by msl-1+t15