Egfrt1/Egfrflb-2E07 animals have rough eyes.
Eggs derived from Egfrt1/Egfrflb-2E07 females are ventralised and have no or only one dorsal appendage.
Homozygous embryos lack all midline glia cells.
Homozygotes display a weak 'flb' phenotype and hemizygotes display an intermediate 'flb' phenotype. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage.
Egfrflb-2E07 has phenotype, non-enhanceable by rhohs.PSt
Egfrflb-2E07/Egfrt1 has eye phenotype, suppressible by kek1RA5/kek1RM2
Egfrflb-2E07/Egfrt1 has eye phenotype, suppressible | partially by kek1RA5/kek1[+]
Egfrflb-2E07/Egfrt1 has eye phenotype, suppressible | partially by kek1[+]/kek1RM2
Egfrflb-2E07/Egfrt1 has dorsal appendage phenotype, suppressible | partially by kek1RA5/kek1RM2
Egfrflb-2E07 has phenotype, non-suppressible by rhohs.PSt
The Egfrt1/Egfrflb-2E07 phenotype is partially suppressed by kek1RA5/kek1RM2.
The ubiquitous expression of rhohs.PSt under heatshock has no effect on Egfrflb-2E07 embryos.
Mutation of Egfr that coordinately affects all gene activities, a class I lesion. The allelic series for class I lesions: Egfrt2 = Egfrt1 < Egfrtop-EC20 < Egfrf7 = Egfrf1 = Egfrflb-2E07 < Egfrtop-EE39 = Egfrtop-ED26 = Egfrf5 < Egfrf9 = Egfrf10 = Egfrf2 = Egfrtop-EE42 = Egfrf11 = Egfrf24 = Egfrf3 = Df(2R)Egfr3.
Weak Egfr allele.