XB-FEAT-1011225: Difference between revisions
Jump to navigation
Jump to search
imported>Xenbase (→mmut) |
imported>Xenbase |
||
| (One intermediate revision by the same user not shown) | |||
| Line 5: | Line 5: | ||
10.23.2018 | 10.23.2018 | ||
Human symbol has changed for genepage ID: 1011225 From mut to MMUT | Human symbol has changed for genepage ID: 1011225 From mut to MMUT | ||
Human symbol has changed for Entrez Gene: 4594. From MUT to MMUT | Human symbol has changed for Entrez Gene: 4594. From MUT to MMUT | ||
=Summary from NCBI= | |||
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] | |||
Latest revision as of 07:20, 23 October 2018
mmut
This is the community wiki page for the gene mmut please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
nomenclature changes
10.23.2018 Human symbol has changed for genepage ID: 1011225 From mut to MMUT
Human symbol has changed for Entrez Gene: 4594. From MUT to MMUT
Summary from NCBI
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]