| Gene Symbol | MCCC2 |
| Entrez Gene ID | 64087 |
| Full Name | methylcrotonoyl-CoA carboxylase 2 |
| Synonyms | MCCB |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. [provided by RefSeq, Jul 2008]. |
| Disorder MIM: | |
| Disorder Html: | 3-Methylcrotonyl-CoA carboxylase 2 deficiency, 210210 (3) |

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