kek1RA5/kek1RM2 is a suppressor of eye phenotype of Egfrflb-2E07/Egfrt1
kek1RA5/kek1[+] is a suppressor | partially of eye phenotype of Df(2R)Egfr3/Egfrt1
kek1RA5/kek1[+] is a suppressor | partially of eye phenotype of Egfrflb-2E07/Egfrt1
kek1RA5/kek1RM2 is a suppressor of wing vein L4 phenotype of Egfrt1/Egfrf24
kek1RA5/kek1RM2 is a suppressor | partially of dorsal appendage phenotype of Egfrflb-2E07/Egfrt1
Nrt5, kek1RA5/kek1RM2 has axon | embryonic stage phenotype
Nrt5, kek1RA5 has axon | embryonic stage phenotype
Heterozygous kek1RA5 partially suppresses the rough eye phenotype seen Egfrf24/Egfrt1 animals. Heterozygous kek1RA5 partially suppresses the rough eye phenotype seen Egfrflb-2E07/Egfrt1 animals. kek1RM2/kek1RA5 fully suppresses the phenotype. Heterozygous kek1RA5 partially suppresses the rough eye phenotype seen Df(2R)Egfr3/Egfrt1 animals.
Extension of longitudinal axons through the intercommissural region is frequently abnormal in kek1RA5/kek1RM2; Nrt5 embryos. In addition, Fas2 expressing axons show defasciculation, stalling and guidance defects, including crossing of the midline. The stalling and misguidance phenotypes can be rescued by NrtScer\UAS.cSa expressed under the control of Scer\GAL4Mz1277.