Automated description from the Alliance of Genome Resources (Release 7.0.0)
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; nucleolus; and nucleoplasm. 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).