Amino acid replacement: Y148N.
T21778972A
Y148N | tsl-PA; Y148N | tsl-PB; Y148N | tsl-PC
Y148N
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
filzkorper | embryonic stage | maternal effect (with tslΔ)
telson | embryonic stage | maternal effect (with tslΔ)
Late embryos from tsl5/tslΔ transheterozygous mothers exhibit a fully penetrant "terminal class mutant" phenotype, in which some terminal structures are missing (including head structures, abdominal segment 8, telson, and filzkorper), and exhibit a highly penetrant posterior-ventral cuticle hole phenotype, as compared to controls.
Allelic series: tsl5 = tsl4 > tsl3 > tsl1 > tsl2