| Gene Symbol | TMEM126A |
| Entrez Gene ID | 84233 |
| Full Name | transmembrane protein 126A |
| Synonyms | OPA7 |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]. |
| Disorder MIM: | |
| Disorder Html: | Optic atrophy 7, 612989 (3) |

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