| Gene Symbol | MECR |
| Entrez Gene ID | 51102 |
| Full Name | mitochondrial trans-2-enoyl-CoA reductase |
| Synonyms | CGI-63,DYTOABG,ETR1,FASN2B,NRBF1 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy. [provided by RefSeq, Mar 2017]. |
| Disorder MIM: | |
| Disorder Html: | Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities, 617282 (3) |









































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