Lesion present between 50.3 and 53.5kb downstream of zero (zero being 973bp proximal to the pk transcription start site.).
Causes no embryonic phenotype even when homozygous mutant embryos develop from homozygous mutant mothers. Has a weak polarity phenotype in the wing, notum, abdomen, eye and legs. Denticle belt morphology and denticle orientation remains wild-type.
pkpk-sple-26 is an enhancer of abnormal cell polarity phenotype of Scer\GAL4hs.2sev, VangUAS.cWa
pkpk-sple-26 is an enhancer of ommatidium phenotype of Scer\GAL4hs.2sev, VangUAS.cWa
D. Coulson.