MMAA, metabolism of cobalamin associated A

MMAA, metabolism of cobalamin associated A

• The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008]

• Gene Synonyms (methylmalonic aciduria type A protein, mitochondrial, methylmalonic aciduria (cobalamin deficiency) cblA type, mutant adenosylcobalamin, cblA,)
• NCBI Gene ID: 166785
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q8IVH4
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

metabolism of cobalamin associated A interacts with:

• metabolism of cobalamin associated A

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