CPRiL

Protein Name	methylmalonyl-CoA mutase
Organism	Homo sapiens
Gene ID	4594
Gene Symbol	MMUT
UniProt	P22033 (MUTA_HUMAN), A0A024RD82 (A0A024RD82_HUMAN), B2R6K1 (B2R6K1_HUMAN)
Relationships	Total Number of functionally related compound(s) : 219 Total Number of Articles : 240
Description	methylmalonyl-CoA mutase
Gene Summary	This gene encodes the mitochondrial enzyme methylmalonyl Coenzyme A mutase. In humans, the product of this gene is a vitamin B12-dependent enzyme which catalyzes the isomerization of methylmalonyl-CoA to succinyl-CoA, while in other species this enzyme may have different functions. Mutations in this gene may lead to various types of methylmalonic aciduria. [provided by RefSeq, Jul 2008]
synonyms	methylmalonyl-CoA mutase, mitochondrial methylmalonyl Coenzyme A mutase methylmalonyl-CoA isomerase methylmalonyl-CoA mutase c.192delA methylmalonyl-CoA mutase c.51C>G methylmalonyl-CoA mutase variant c.1495G>A methylmalonyl-CoA mutase variant c.2011A>G methylmalonyl-CoA mutase variant c.2150G>T methylmalonyl-CoA mutase variant c.322C>T methylmalonyl-CoA mutase variant c.613_615delGAA methylmalonyl-CoA mutase variant c.636G>A methylmalonyl-CoA mutase variant c.643G>A mutant methylmalonyl CoA mutase MCM MUT Click to show/hide the synonyms
Properties