MDH1 Chromosome 2
Malate dehydrogenase 1
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What This Gene Does
This gene encodes an enzyme that catalyzes the NAD/NADH-dependent, reversible oxidation of malate to oxaloacetate in many metabolic pathways, including the citric acid cycle. Two main isozymes are known to exist in eukaryotic cells: one is found in the mitochondrial matrix and the other in the cytoplasm. This gene encodes the cytosolic isozyme, which plays a key role in the malate-aspartate shuttle that allows malate to pass through the mitochondrial membrane to be transformed into oxaloacetate for further cellular processes. Alternatively spliced transcript variants have been found for this gene. A recent study showed that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Pseudogenes have been identified on chromosomes X and 6. [provided by RefSeq, Feb 2016]
Gene Info
Gene Group
Malate dehydrogenases
Locus Type
gene with protein product
Location
2p15
Ensembl
ENSG00000014641
Associated Conditions (2)
Developmental and epileptic encephalopathy
88
All Variants (1)
| RSID | Category | Clinical Significance | Conditions |
|---|---|---|---|
| RS1709340590 | Health Risk | Pathogenic | Developmental and epileptic encephalopathy, 88, Developmental and epileptic encephalopathy |