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SDHA (NM_001294332) - succinate dehydrogenase complex flavoprotein subunit A
Succinate Dehydrogenase [Ubiquinone] Flavoprotein Subunit, Mitochondrial Isoform 2
Legend
Mutation impacts
direct
network-rewiring
motif-changing
proximal
distal
none
Sites
multiple types
acetylation
methylation
succinylation
sumoylation
ubiquitination
glycosylation
- C-linked
- N-linked
- O-linked
- S-linked
phosphorylation
- SARS-CoV-2
Others
Exact position of a PTM site
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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
External references
Mappings retrieved from NCBI & UniProt.