Imprecise excision of the P{lArB} insertion.
No major abnormalities are seen in the CNS of homozygous embryos, although partial defasciculation of Fas2 expressing axon bundles is occasionally seen.
kek1RA5/kek1RM2 is a suppressor of eye phenotype of Egfrflb-2E07/Egfrt1
kek1[+]/kek1RM2 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, kek1RM2 has axon | embryonic stage phenotype
Nrt5, kek1RA5/kek1RM2 has axon | embryonic stage phenotype
Extension of longitudinal axons through the intercommissural region is frequently abnormal in kek1RM2; Nrt5 and 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.