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SDHA (NM_001294332) - succinate dehydrogenase complex flavoprotein subunit A

Succinate Dehydrogenase [Ubiquinone] Flavoprotein Subunit, Mitochondrial Isoform 2

Mutations Visualisation

Protein summary

This is an alternative isoform of SDHA protein. View all 2 isoforms
SDHA: succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial isoform 2
Description:

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].

Strand
+
Chromosome
5
Protein
616 residues
All mutations
603
PTM sites
38
CDS
218,470 - 256,535
Transcription
218,337 - 257,197
8.28% of sequence is predicted to be disordered

External references

Mappings retrieved from NCBI & UniProt.
RefSeq
Entrez
gene: 6389
UniProt
Ensembl