Automated description from the Alliance of Genome Resources
Predicted to have ribitol beta-1,4-xylosyltransferase activity. Predicted to be involved in protein O-linked mannosylation. Localizes to the Golgi apparatus. Human ortholog(s) of this gene implicated in congenital muscular dystrophy-dystroglycanopathy type A10. Is expressed in forelimb bud. Orthologous to human RXYLT1 (ribitol xylosyltransferase 1).