Mutation results in an ectopic splice acceptor site in an intron, resulting in a frameshift from amino acid residue 13.
Nucleotide substitution: G138A.
G26043481A
G138A
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.
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 hryUAS.cIa
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.