E(bx)ry122 mutants show class I dendrite branching defects at late larval stages.
E(bx)ry122 mutants have a high incidence of melanotic tumours and an increased number of larval hemocytes.
The male X chromosome in E(bx)ry122/Df(3L)3643 mutants is highly aberrant. E(bx)Nurf301-2/E(bx)ry122 and E(bx)ry122/E(bx)Nurf301-3 mutant larvae exhibit melanotic tumours.
E(bx)ry122 has neoplasia phenotype, non-suppressible by Df(2R)ED3921
E(bx)ry122/E(bx)[+] is an enhancer of visible | dominant phenotype of gcmPyx
E(bx)ry122 has embryonic/larval hemocyte | increased number phenotype, non-suppressible by Df(2R)ED3921
E(bx)ry122/E(bx)[+] is an enhancer of chaeta | increased number phenotype of gcmPyx
E(bx)ry122/E(bx)[+] is an enhancer of dorsal appendage | maternal effect phenotype of EcRB1-ΔC655.F645A.UAS, Scer\GAL4slbo.2.6
E(bx)ry122 is an enhancer of adult metathoracic segment phenotype of Ubx6.28/Ubxbx-34e
E(bx)ry122 is an enhancer of haltere phenotype of Ubx6.28/Ubxbx-34e
E(bx)ry122 is an enhancer of wing | ectopic phenotype of Ubx6.28/Ubxbx-34e
E(bx)ry122 is an enhancer of adult mesothoracic segment | anterior | ectopic phenotype of Ubx6.28/Ubxbx-34e
Df(2R)ED3921 fails to suppress the melanotic tumour and increased larval hemocyte number of E(bx)ry122 mutants.
The frequency of abnormal dorsal appendages in embryos derived from females carrying EcRB1-ΔC655.F645A.Scer\UAS under the control of Scer\GAL4slbo.2.6 (23%) is increased if the females are also heterozygous for E(bx)ry122 (84%).
A. Spradling.