MDH1 Chromosome 2

Malate dehydrogenase 1
1 variant 1 Health Risk

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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
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS1709340590 Health Risk Pathogenic Developmental and epileptic encephalopathy, 88, Developmental and epileptic encephalopathy
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