MMUT wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human MMUT wild-type allele is located in the vicinity of 6p12.3 and is approximately 33 kb in length. This allele, which encodes methylmalonyl-CoA mutase, mitochondrial protein, plays a role in the metabolism of fatty acid-coenzyme A intermediates in the tricarboxylic acid cycle. Mutations in the gene are associated with methylmalonic aciduria types mut(0) and mut(-).

**Synonyms:** - MCM - MUT - Methylmalonyl Coenzyme A Mutase Gene - Methylmalonyl-CoA Mutase wt Allele