Insertion of a roo element (in antiparallel orientation) into the 5' untranslated region.
Insert stated as cause: undefined Insertion of a retrotransposon into 5' leader sequences.
roo insertion into 5' untranslated leader.
Retrotransposon in 5' leader of w gene.
Antiparallel roo insertion into 5' untranslated leader sequence.
Unknown.
wbf2 has abnormal eye color | recessive phenotype, enhanceable by Low1
wbf2 has pigment cell phenotype, enhanceable by Low1
wbf2 has pigment cell phenotype, suppressible by In(3)Msu1/+
wbf2 has pigment cell phenotype, suppressible by In(3)Msu2/+
In(3)Msu2/In(3)Msu1, wbf2 has pigment cell phenotype
Oliver, 16th Nov. 1932.