Automated description from the Alliance of Genome Resources
Predicted to have mannose-1-phosphate guanylyltransferase activity. Predicted to be involved in biosynthetic process. Localizes to the mitochondrion. Human ortholog(s) of this gene implicated in Walker-Warburg syndrome; autosomal recessive limb-girdle muscular dystrophy type 2T; and muscular dystrophy-dystroglycanopathy. Orthologous to human GMPPB (GDP-mannose pyrophosphorylase B).