FH (NM_000143) - fumarate hydratase
Fumarate Hydratase, Mitochondrial
Legend
Mutation impacts
Sites
- C-linked
- N-linked
- O-linked
- S-linked
- SARS-CoV-2
Others
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Mutations Visualisation
Protein summary
The protein encoded by this gene is an enzymatic component of the tricarboxylic acid (TCA) cycle, or Krebs cycle, and catalyzes the formation of L-malate from fumarate. It exists in both a cytosolic form and an N-terminal extended form, differing only in the translation start site used. The N-terminal extended form is targeted to the mitochondrion, where the removal of the extension generates the same form as in the cytoplasm. It is similar to some thermostable class II fumarases and functions as a homotetramer. Mutations in this gene can cause fumarase deficiency and lead to progressive encephalopathy. [provided by RefSeq, Jul 2008].
Publication Note:
This RefSeq record includes a subset of the publications that are available for this gene. Please see the Gene record to access additional publications.
Evidence data:
Transcript exon combination :: U59309.1, BC003108.1 [ECO:0000332]
- Strand
- -
- Chromosome
- 1
- Protein
- 510 residues
- All mutations
- 432
- PTM sites
- 32
- CDS
- 241,661,127 - 241,683,022
- Transcription
- 241,660,856 - 241,683,085