Amino acid replacement: W995term.
G7146468A
W995term | gfzf-PB; W184term | gfzf-PD; W995term | gfzf-PE
W995term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified). Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
gfzfCK438 can suppress the lethal interaction between pn18a and transgenic awdKpn.cPa.
Based on the extent of suppression of pn18a-awdKpn.cPa lethality, the following gfzf alleles can be ranked from the strongest to the weakest as follows: gfzfSu(Kpn)2 > gfzfBU640 > gfzfDC727 > gfzfAP320 > gfzfCK438 > gfzfCZ811 > gfzfSu(Kpn)1 > gfzfAP434 > gfzfCX322 > gfzfBX123 > gfzfBW914 = gfzfAB621 > gfzfSu(Kpn)3 > gfzfBS304 > gfzfCU338 > gfzfDC806 = gfzfCL1027 > gfzfAV739 > gfzfAB924.