hypomorphic allele - genetic evidence
Amino acid replacement: C425Y.
C9635823G
C425W | Scm-PA; C425W | Scm-PB
C425Y|FBrf0104734
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
ScmK2 is an enhancer of visible | dominant | homeotic phenotype of Pc3
ScmK2, ph-p409 has partially lethal phenotype
ScmK2 is a suppressor of phenotype of z1
Dominantly enhances the homeotic phenotypes of Pc3/+ adults. ph-p409 males that are also heterozygous for ScmK2 show partial lethality.
Scm4