Amino acid replacement: C422Y. C422 falls in the RING domain.
G16038724A
C422Y | Diap1-PA; C422Y | Diap1-PB; C422Y | Diap1-PC; C422Y | Diap1-PD; C422Y | Diap1-PE; C422Y | Diap1-PF
C422Y
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. C422 falls in the RING domain.
Embryos show increased cell death as assessed by TUNEL staining. Development proceeds further in development than do the loss of function alleles.
Embryos exhibit defects in cellularization.
Diap181.03 is an enhancer of abnormal cell death phenotype of rprGMR.PW
Diap181.03 is an enhancer of abnormal cell death phenotype of grimGMR.PC
Diap181.03 is a suppressor of abnormal cell death phenotype of hidGMR.PG
Diap181.03 is an enhancer of eye phenotype of rprGMR.PW
Diap181.03 is an enhancer of eye phenotype of grimGMR.PC
Diap181.03 is a suppressor of eye phenotype of hidGMR.PG
One of 6 th mutants isolated.