Deletion of sequences in the 5' regulatory region.
Deficiency in 5' regulatory region.
Deficiency in 5' cis-regulatory region.
Deficiency in 5' cis regulatory region.
Deletion of 1kb between nucleotide positions -2200 and -1029.
Deletion of 1.1kb from map position +4.9 to +6.0 relative to the transcription start site of w.
Deletion of 1.2kb between coordinates +5 and +6.4, using coordinate system of FBrf0038648 where coordinate 0 is the copia insert of wa.
deletion in regulatory region map site (kb): +4.78 to +5.85; Origin = insertion of wa copia; '-' values to left (telomere) end; '+' values to right (centromere) end.
Deletion endpoints from FBrf0041384 and GB:X02974.
Fails to respond to E(wa).
Phenotype is not affected by Doa mutations.
Eye colour: yellowish to brown; fine-grained mottling; male darker than female.
wsp4 has abnormal eye color phenotype, enhanceable by zv77h
wsp4 has abnormal eye color phenotype, enhanceable by z1
wsp4, zv77h has abnormal eye color phenotype, enhanceable by Taf91
wsp4, z1 has abnormal eye color phenotype, enhanceable by Taf91
wsp4, zv77h has abnormal eye color phenotype, enhanceable by e(y)21
wsp4, zv77h has abnormal eye color phenotype, enhanceable by e(y)34
wsp4, z1 has abnormal eye color phenotype, enhanceable by e(y)34
wsp4, zop6 has abnormal eye color phenotype, enhanceable by e(y)34
wsp4, zop6R1 has abnormal eye color phenotype, enhanceable by e(y)34
wsp4, z1 has abnormal eye color phenotype, non-enhanceable by e(y)21
wsp4 has pigment cell phenotype, enhanceable by zv77h
wsp4 has pigment cell phenotype, enhanceable by z1
wsp4, zv77h has pigment cell phenotype, enhanceable by Taf91
wsp4, z1 has pigment cell phenotype, enhanceable by Taf91
wsp4, zv77h has pigment cell phenotype, enhanceable by e(y)21
wsp4, zv77h has pigment cell phenotype, enhanceable by e(y)34
wsp4, z1 has pigment cell phenotype, enhanceable by e(y)34
wsp4, zop6 has pigment cell phenotype, enhanceable by e(y)34
wsp4, zop6R1 has pigment cell phenotype, enhanceable by e(y)34
LeFever.