Gene information for SDHA (Homo sapiens)
(Information is obtained from NCBI Gene database)
| Entrez gene ID | 6389 |
| Official gene symbol | SDHA |
| Full name | succinate dehydrogenase complex, subunit A, flavoprotein (Fp) |
| Aliases | ,FP,SDH1,SDH2,SDHF, |
| Gene summary | This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. [provided by RefSeq] |
| Location | Chromosome: 5 Locus: |
| Gene position | 218356 - 256815 Map Viewer |
| OMIM ID | 600857 |
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