Automated description from the Alliance of Genome Resources
Predicted to have phosphomannomutase activity. Predicted to be involved in mannose metabolic process; protein N-linked glycosylation; and protein targeting to ER. Localizes to the cytoplasm and neuronal cell body. Used to study congenital disorder of glycosylation type I. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation. Orthologous to human PMM2 (phosphomannomutase 2).