Complex deletion and change that leads to an 8-amino acid deletion/1-amino acid substitution lacking the first 4 amino acid residues of the AH1 helix (amino acids 19-27 are deleted and the 19th residue is changed from Pro to Ser).
delta191-214
Delta19-27
In frame deletion of residues 19-27 that, together with the adjacent C-to-T nucleotide change just upstream, results in replacement of PIKFTIADT peptide with a single Serine codon. One of three nucleotide changes observed in gro[MB5] mutant. Position of mutation on reference sequence inferred by FlyBase curator.
T26043532C
T189C
G18G | gro-PA; G18G | gro-PB; G18G | gro-PC; G18G | gro-PD; G18G | gro-PE; G18G | gro-PF; G18G | gro-PG; G18G | gro-PH; G18G | gro-PI; G18G | gro-PJ
One of three nucleotide changes observed in gro[MB5] mutant. Position of mutation on reference sequence inferred by FlyBase curator.
C26043533T
C190T
P19S | gro-PA; P19S | gro-PB; P19S | gro-PC; P19S | gro-PD; P19S | gro-PE; P19S | gro-PF; P19S | gro-PG; P19S | gro-PH; P19S | gro-PI; P19S | gro-PJ
P19S
One of three nucleotide changes observed in gro[MB5] mutant. Position of mutation on reference sequence inferred by FlyBase curator.
Mutant embryos show loss of alternate ventral denticle belts. This segmentation phenotype is weak, with usually only 2-3 even-numbered denticle belts being missing (0% are wild type, 5% lack one belt, 27% lack two belts, 52% lack three belts and 16% lack more than three belts).
groMB5/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.