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This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group.
9130222L19Rik; aquocob(I)alamin vitamin B12s adenosyltransferase; ATP:Cob(I)alamin Adenosyltransferase; ATP:corrinoid adenosyltransferase; ATR; cblB; CFAP23; cilia and flagella associated protein 23; cob; cob(I)alamin adenosyltransferase; cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial; Cob(II)alamin adenosyltransferase; Cob(II)yrinic acid a,c-diamide adenosyltransferase; Cobinamide/cobalamin adenosyltransferase; Corrinoid adenosyltransferase; methylmalonic aciduria (cobalamin deficiency) cblB type; methylmalonic aciduria (cobalamin deficiency) type B homolog (human); methylmalonic aciduria type B homolog; Methylmalonic aciduria type B protein; Mmab
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