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. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]
- Tricarboxylic acid cycle
- Succinate metabolic process
- Mitochondrial electron transport, succinate to ubiquinone
- Nervous system development
- Electron transport chain
- Mitochondrial complex ii deficiency
- Cardiomyopathy, dilated, 1gg
- Paragangliomas 5
- Leigh syndrome
- Hereditary paraganglioma-pheochromocytoma syndromes
SDHA. Johnhfst.