| Gene Symbol | NDUFA9 |
| Entrez Gene ID | 4704 |
| Full Name | NADH:ubiquinone oxidoreductase subunit A9 |
| Synonyms | CC6,CI-39k,CI39k,NDUFS2L,SDR22E1 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | The encoded protein is a subunit of the hydrophobic protein fraction of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. A pseudogene has been identified on chromosome 12. [provided by RefSeq, May 2010]. |
| Disorder MIM: | |
| Disorder Html: | Leigh syndrome due to mitochondrial complex I deficiency, 256000 (3) |
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