ommatidium (with Egfrt1)
wing vein L4 (with Egfrt1)
Loss of Egfr function reduces the number of glial cells in stage 12 embryos and in later embryos these cells die.
Clonal analysis in eye, antenna, wing and leg discs suggests that Egfr- cells do not proliferate as well as wild type. Egfr cells in the eye disc are unable to differentiate as photoreceptor cells, and cells lacking Egfr function can perturb the developmental fate of their neighbors.
Suppresses the "Ellipse" phenotype.
The viability of homozygous clones in the wing is very low. Homozygous clones in the legs, notum and head seem to be inviable. Homozygous clones in the abdominal tergites are viable. Wild-type chaetae are clustered immediately adjacent to or included within these clones and there is a depletion of chaetae around the clones for several cell diameters.
Homozygotes and hemizygotes display a severe 'flb' phenotype. Embryos produced from heteroallelic combination with Egfrt1 have a severe ventralised phenotype, reduction in size of their dorsal appendage.
severe allele
Egfrt1/Egfrf11 has abnormal planar polarity phenotype, suppressible | partially by fz[+]/fz21
Egfrt1/Egfrf11 has abnormal planar polarity phenotype, suppressible | partially by fz23/fz[+]
Egfrt1/Egfrf11 has phenotype, enhanceable by rhounspecified/rhounspecified
Egfrt1/Egfrf11 has phenotype, enhanceable by vnunspecified/vnunspecified
Egfrt1/Egfrf11 has phenotype, enhanceable by ciunspecified/ciunspecified
Egfrt1/Egfrf11 has phenotype, enhanceable by astunspecified/astunspecified
Egfrt1/Egfrf11 has phenotype, enhanceable by vvlunspecified/vvl[+]
Egfrt1/Egfrf11 has ommatidium phenotype, suppressible | partially by fz[+]/fz21
Egfrt1/Egfrf11 has ommatidium phenotype, suppressible | partially by fz23/fz[+]
Egfrt1/Egfrf11 has anterior crossvein phenotype, suppressible | partially by ash2[+]/ash2I1
Egfrt1/Egfrf11 has wing vein L4 phenotype, suppressible | partially by ash2[+]/ash2I1
Egfrt1/Egfrf11 has wing vein L4 phenotype, suppressible by sty[+]/styS73
Egfrt1/Egfrf11 has anterior crossvein phenotype, suppressible by sty[+]/styS73
Egfrt1/Egfrf11 has wing vein L4 phenotype, suppressible by sty[+]/styS88
Egfrt1/Egfrf11 has anterior crossvein phenotype, suppressible by sty[+]/styS88
Egfrt1/Egfrf11 has phenotype, suppressible by netunspecified/netunspecified
Egfrt1/Egfrf11 has phenotype, suppressible by tkvunspecified/tkvunspecified
Egfrt1/Egfrf11 has wing vein phenotype, suppressible by netunspecified/netunspecified
Egfrt1/Egfrf11 is an enhancer of phenotype of vvlunspecified
Egfrt1/Egfrf11 is an enhancer of phenotype of ciunspecified
Egfrt1/Egfrf11 is an enhancer of phenotype of astunspecified
Egfrt1/Egfrf11 is an enhancer of phenotype of vnunspecified
Egfrf11 is a suppressor of photoreceptor cell R1 | ectopic phenotype of B-H1sev.PH
Egfrf11 is a suppressor of photoreceptor cell R2 | ectopic phenotype of B-H1sev.PH
Egfrf11 is a suppressor of photoreceptor cell R3 | ectopic phenotype of B-H1sev.PH
Egfrf11 is a suppressor of photoreceptor cell R4 | ectopic phenotype of B-H1sev.PH
Egfrf11 is a suppressor of photoreceptor cell R5 | ectopic phenotype of B-H1sev.PH
Egfrf11 is a suppressor of photoreceptor cell R6 | ectopic phenotype of B-H1sev.PH
Egfrt1/Egfrf11 is a suppressor of wing vein phenotype of netunspecified
Egfrt1/Egfrf11 is a suppressor of phenotype of tkvunspecified
Egfrf11 is a non-suppressor of photoreceptor cell R7 phenotype of B-H1sev.PH
BacA\p35GMR.PH, Egfrf11 has eye photoreceptor cell phenotype
Egfrf11, rl1 has wing vein L4 phenotype
Only R8 photoreceptor cells differentiate in Egfrf11 clones which are also expressing BacA\p35GMR.PH. Some mutant cells differentiate small photoreceptor rhabdomeres; most cells resemble pigment cells morphologically, but contain little pigment.
Egfrf11 significantly suppresses the formation of extra outer photoreceptors caused by B-H1sev.PH, although it does not affect the loss of R7 cell phenotype caused by B-H1sev.PH.
Suppressor of the dosage-dependent (two or more copies of P{sev-svp1} or P{sev-svp2}) transformation of cone cells into R7 photoreceptors and at a lower frequency R7 cells into outer photoreceptors.
Double mutant combinations of Egfrt1/Egfrf11 with rhounspecified/rhounspecified, vnunspecified/vnunspecified, ciunspecified/ciunspecified, astunspecified/astunspecified, tt1/tt1, Vnounspecified/+, H2/+, vvlunspecified/+ or NAx-M1/+ have a superadditive phenotype. Double mutant combinations of Egfrt1/Egfrf11 with kn1/kn1 or netunspecified/netunspecified show mutual suppression, with both the Egfr and vein phenotypes being normalised. Egfrt1/Egfrf11 shows a negative interaction in combination with either DlM1/+ or tkvunspecified/tkvunspecified. Egfrt1/Egfrf11 shows a simple additive phenotype with dppunspecified/dppunspecified, kniunspecified/kniunspecified, tg2/tg2, cv-2unspecified/cv-2unspecified and N55e11/+. E(spl)rv1 grounspecified Egfrt1/Egfrf11 flies show a simple additive phenotype.
Selected as: Embryonic lethal.
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.