|Feature type||allele||Associated gene||Dmel\W|
|Also Known As||hid1|
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|Nature of the Allele|
|Mutations Mapped to the Genome|
|Associated Sequence Data|
|Nature of the lesion|
|Phenotype Manifest In|
Wings remain small and unexpanded. Black spots on head beside proboscis or ocelli. Heterozygous female like homozygote but less extreme. Male much less extreme; wings often expanded but wrinkled, blistered and surface finely pebbled and grayish; no overlap with wild type. Suppressed by D1 in male and nearly so in female. RK1 as dominant.
From prepupal stage through adult, wing bases abnormally narrow, possibly preventing flow of body fluid in sufficient quantity to expand wings.
W[+]/W1 is a suppressor | partially of visible phenotype of LrrkI1915T.Scer\UAS, Scer\GAL4GMR.PF, foxoScer\UAS.cKb
|Phenotype Manifest In|
W[+]/W1 is a suppressor | partially of eye phenotype of LrrkI1915T.Scer\UAS, Scer\GAL4GMR.PF, foxoScer\UAS.cKb
W[+]/W1 is a suppressor of dopaminergic neuron | RU486 conditional phenotype of LrrkI1915T.Scer\UAS, Scer\GAL4elav.Switch.PO, foxoScer\UAS.cKb
W/+ partially suppresses the loss of interommatidial bristles which is seen in bft[Δ263a]/bft[unspecified] flies.
The eye phenotype caused by co-expression of foxo[Scer\UAS.cKb] and Lrrk[I1915T.Scer\UAS] under the control of Scer\GAL4[GMR.PF] is significantly suppressed by W/+. The degeneration of the PPM1/2 and PPL1 neurons which is seen in flies co-expressing foxo[Scer\UAS.cKb] and Lrrk[I1915T.Scer\UAS] under the control of Scer\GAL4[elav.Switch.PO] in the presence of RU486 is suppressed if they alo carry W/+.
|Complementation & Rescue Data|
|Stocks ( 9 )|
|Notes on Origin|
|External Crossreferences & Linkouts|
|Synonyms & Secondary IDs ( 2 )|
|Secondary FlyBase IDs|
|References ( 7 )|