Automated description from the Alliance of Genome Resources (Release 7.4.0)
Predicted to enable mannosyltransferase activity. Acts upstream of or within basement membrane organization; dentate gyrus development; and reactive gliosis. Predicted to be located in cytosol; endoplasmic reticulum membrane; and nuclear lumen. Is expressed in several structures, including central nervous system; craniocervical region bone; gonad; hemolymphoid system gland; and limb. Human ortholog(s) of this gene implicated in lissencephaly and muscular dystrophy (multiple). Orthologous to human POMT2 (protein O-mannosyltransferase 2).
This site uses cookies.
Some cookies are essential for site operations and others help us analyze use and utility of our web site.
Please refer to our
privacy policy
for more information.