| Gene Symbol | SLC25A26 |
| Entrez Gene ID | 115286 |
| Full Name | solute carrier family 25 member 26 |
| Synonyms | COXPD28,SAMC |
| General protein information |
|
| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]. |
| Disorder MIM: | |
| Disorder Html: | Combined oxidative phosphorylation deficiency 28, 616794 (3) |









































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