Automated description from the Alliance of Genome Resources
Predicted to have cob(I)yrinic acid a,c-diamide adenosyltransferase activity and cobalamin binding activity. Predicted to be involved in cobalamin metabolic process. Localizes to the mitochondrion. Human ortholog(s) of this gene implicated in inherited metabolic disorder and methylmalonic acidemia cblB type. Is expressed in several structures, including alimentary system; cardiovascular system; lung; nervous system; and trophectoderm. Orthologous to human MMAB (metabolism of cobalamin associated B).