Nucleotide substitution: GG to AG creating a new splice acceptor, frameshift at thirteenth codon. Same nucleotide substitution as gro[MB15]. Position of mutation on reference sequence inferred by FlyBase curator.
Mutation results in an ectopic splice acceptor site in an intron, resulting in a frameshift from amino acid residue 13.
Nucleotide substitution: G138A.
embryonic/first instar larval cuticle | maternal effect
Embryos derived from homozygous females show severe cuticle loss due to ectopic neurogenesis at the expense of epidermal development.
groMB36/gro[+] is a suppressor of eye phenotype of hUAS.cIa
groMB36 is rescued by gro+t10
groMB36 is partially rescued by groΔSP
groMB36 is not rescued by groΔGP
groMB36 is not rescued by groΔCcN
gro+t10 completely rescues the lethality of groMB36 homozygotes.
groΔGP and groΔCcN each fail to rescue the lethality of groMB36 homozygotes.
groΔSP partially rescues the lethality of groMB36 homozygotes.
Selected as: A modifier of the eye phenotype caused by expression of hScer\UAS.cIa under the control of Scer\GAL4GMR.PF.
groMB15 and groMB36 contain the same lesion.