Insertion of a mdg3 element into the 5' untranslated region.
mdg3 insertion into 5' untranslated leader sequence.
mdg3 insertion in 5' untranslated leader.
Insert stated as cause: undefined Insertion of a copia-like element.
Parallel mdg3 insertion into 5' untranslated region.
Insert stated as cause: undefined Insertion of a retrotransposon near the transcription start site.
Insertion of an unknown transposon near the 5' start site of transcription.
Transposable element near 5' structural gene.
Retrotransposon insertion.
Insert stated as cause: undefined Retrotransposon insertion.
Insertion of a 5.8kb transposable element within the w locus.
eyes have lighter coloring.
Eye colour: mottled with mw.
Eye colour: almost bleach white in homozygous females.
Eye colour: dark yellow in males; lighter in females.
wsp55 has abnormal eye color phenotype, enhanceable by mw1
wsp55 has abnormal eye color | recessive phenotype, suppressible by Rga[+]/Rga03834
wsp55 has abnormal eye color | recessive phenotype, suppressible by Low1
wsp55 has pigment cell phenotype, enhanceable by RpLP001544
wsp55 has pigment cell phenotype, enhanceable by In(3)Msu1/+
wsp55 has pigment cell phenotype, enhanceable by In(3)Msu2/+
wsp55 has phenotype, enhanceable by Ts(YSt;2Lt)B110+Ts(YSt;2Rt)R15
wsp55 has phenotype, enhanceable by Ts(YLt;2Rt)G10+Ts(YLt;2Lt)R155
wsp55 has phenotype, enhanceable by Ts(YSt;2Rt)L107+Ts(YSt;2Lt)P59
wsp55 has phenotype, enhanceable by Ts(YLt;3Lt)A31+Ts(YLt;3Rt)G122
wsp55 has pigment cell phenotype, enhanceable by mw1
wsp55 has phenotype, non-enhanceable by Ts(YLt;3Lt)B141+Ts(YLt;3Rt)G11
wsp55 has phenotype, non-enhanceable by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48
wsp55 has phenotype, non-enhanceable by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128
wsp55 has phenotype, non-enhanceable by Ts(YLt;2Rt)L52+Ts(YLt;2Lt)R15
wsp55 has phenotype, non-enhanceable by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14
wsp55 has phenotype, non-enhanceable by Dp(2;Y)J64
wsp55 has phenotype, non-enhanceable by Ts(YSt;3Rt)A31+Ts(YSt;3Lt)D228
wsp55 has phenotype, non-enhanceable by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36
wsp55 has phenotype, non-enhanceable by Ts(YLt;3Rt)B21+Ts(YSt;3Lt)G11
wsp55 has pigment cell phenotype, suppressible by Rga[+]/Rga03834
wsp55 has pigment cell phenotype, suppressible by Low1
wsp55 has phenotype, suppressible by Ts(YLt;2Rt)B110+Ts(YLt;2Lt)L138
wsp55 has phenotype, suppressible by Ts(YLt;3Lt)B141
wsp55 has phenotype, suppressible by Ts(YLt;3Lt)B21
wsp55 has phenotype, non-suppressible by Ts(YLt;2Rt)L52+Ts(YLt;2Lt)R15
wsp55 has phenotype, non-suppressible by Ts(YSt;2Lt)H149+Ts(YSt;2Rt)R14
wsp55 has phenotype, non-suppressible by Dp(2;Y)J64
wsp55 has phenotype, non-suppressible by Ts(YSt;3Rt)A31+Ts(YSt;3Lt)D228
wsp55 has phenotype, non-suppressible by Ts(YSt;3Lt)G48+Ts(YSt;3Rt)R36
wsp55 has phenotype, non-suppressible by Ts(YLt;3Rt)B21+Ts(YSt;3Lt)G11
wsp55 has phenotype, non-suppressible by Ts(YLt;3Lt)B141+Ts(YLt;3Rt)G11
wsp55 has phenotype, non-suppressible by Ts(YLt;3Lt)B116+Ts(YLt;3Rt)G48
wsp55 has phenotype, non-suppressible by Ts(YSt;3Rt)G73+Ts(YSt;3Lt)R128
sgl05007, wsp55 has pigment cell phenotype
Shows hyper-dosage compensation.
Wow mutations dominantly cause a reduction of w pigmentation.
The alkylating agents EMS, MMS, and ENU induce a clear increase in the frequency of somatic revertant sectors in the eye in wsp55 flies.