The premature stop codon is predicted to result in a truncated protein that lacks most of the wild-type sequence including the MAPK phosphorylation sites and the entire ETS DNA-binding domain.
Amino acid replacement: Q111term.
C2160161T
Q111term | aop-PA; Q111term | aop-PB; Q111term | aop-PC; Q111term | aop-PD; Q111term | aop-PE
Q111term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
abnormal cell number | adult stage (with aopE833), with aopV105R.GFP
eye (with aopE833), with aopV105R.GFP
eye photoreceptor cell (with aopE833), with aopV105R.GFP
eye photoreceptor cell | ectopic (with aopE833), with aopV105R.GFP
Adult aop443/aopE833 transheterozygotes bearing aopV105R.GFP show a rough eye phenotype; most ommatidia show extra photoreceptor cells, particularly inner photoreceptor R7 cells, but some other miss photoreceptor cells, as compared to controls.
The majority of border cells in egg chambers with aop443 mutant clones fail to migrate. The border cells are connected laterally to squamous follicle cells, suggesting that they remain attached to the anterior follicular epithelium.
aop443/aop[+] is an enhancer of abnormal planar polarity phenotype of Scer\GAL4hs.2sev, dgoUAS.cFa
aop443/aop[+] is an enhancer of ommatidium phenotype of Scer\GAL4hs.2sev, dgoUAS.cFa
aop443/aop[+] is a non-enhancer of wing hair phenotype of Scer\GAL4hs.2sev, dgoUAS.cFa
aop443/aop[+] is a non-suppressor of wing hair phenotype of Scer\GAL4hs.2sev, dgoUAS.cFa
aop443/+ enhances the planar cell polarity (PCP) defects in the eye induced by the overexpression of dgoScer\UAS.cFa under the control of Scer\GAL4hs.2sev.
Selected as: a modifier of Ras85D in the eye in a genetic screen.