Amino acid replacement: G566D. Nucleotide substitution: G2675A. Co-ordinates refer to the pNB36C cDNA.
A strong missense mutation.
G23749365A
G2675A
G566D | Hmgcr-PA
G566D
Primordial germ cell migration is disrupted. Some PGCs fail to migrate from the endoderm to the mesoderm. Many of those that do fail to associate with the gonadal mesoderm and remain scattered throughout the embryo. Gonadal mesoderm development proceeds normally, as does development of the nervous system and the trachea.
Hmgcrclb2 is a suppressor of adult brain phenotype of SNF4Aγloe
Strong allele.