Involved in cobalamin metabolism.
CblD; likely ortholog of H. sapiens chromosome 2 open reading frame 25 (C2orf25); methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria; Methylmalonic aciduria and homocystinuria type D homolog, mitochondrial; Methylmalonic aciduria and homocystinuria type D protein, mitochondrial; protein C2orf25, mitochondrial
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