Nucleotide substitution: G3305A. Amino acid replacement: V911M. This mutation is in the cytoplasmic domain of the protein.
G26840584A
G3305A
V911M | Tl-PB; V911M | Tl-PC; V911M | Tl-PD
V911M
This mutation is in the cytoplasmic domain of the protein.
Recessive.
Embryos from homozygous females are moderately dorsalised.
Moderate dorsalization of embryo.
Completely penetrant phenotype.