4bp substitution that changes two consecutive amino acids in the N-terminus of the protein. Amino acid replacement: L50S. Amino acid replacement: R51G.
L50S|ksr-PA
R51G|ksr-PA
L50S
R51G
A 4bp substitution that changes two consecutive amino acids. The amino acid changes are L50S and R51G.
AGTG
Few ommatidia contain the normal complement of receptor cells.
Homozygotes are subviable and have rough eyes.
ksrS-548 has visible | recessive phenotype, suppressible by PTP-ERXE-3022
ksrS-548 has visible | recessive phenotype, suppressible by PTP-ERXE-2776
ksrS-548 has visible phenotype, suppressible by aopyan-XE18
ksrS-548 has eye phenotype, suppressible by PTP-ERXE-3022
ksrS-548 has ommatidium phenotype, suppressible by PTP-ERXE-3022
ksrS-548 has photoreceptor neuron phenotype, suppressible by PTP-ERXE-3022
ksrS-548 has eye phenotype, suppressible by PTP-ERXE-2776
ksrS-548 has ommatidium phenotype, suppressible by PTP-ERXE-2776
ksrS-548 has photoreceptor neuron phenotype, suppressible by PTP-ERXE-2776
ksrS-548 has eye photoreceptor cell phenotype, suppressible by aopyan-XE18
ksrS-548 has eye photoreceptor cell phenotype, suppressible by ttk190.1
ksrS-548 is a suppressor of eye phenotype of Ras85DV12.sev
Heterozygous PTP-ERXE-3022, PTP-ERXE-2776 as well as deficiency alleles of PTP-ER suppress the rough eyes and loss of photoreceptor cells seen in homozygous ksrS-548.
Up to 99% ommatidia are wild type in a aopyan-XE18 or ttk190.1 mutant background.
Dominantly suppresses the rough eye phenotype of Ras85DV12.sev.