IDH1 Chromosome 2

Isocitrate dehydrogenase (NADP(+)) 1
4 variants 4 Health Risk

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What This Gene Does
Isocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2-oxoglutarate. These enzymes belong to two distinct subclasses, one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+)-dependent isocitrate dehydrogenases, which localize to the mitochondrial matrix, and two NADP(+)-dependent isocitrate dehydrogenases, one of which is mitochondrial and the other predominantly cytosolic. Each NADP(+)-dependent isozyme is a homodimer. The protein encoded by this gene is the NADP(+)-dependent isocitrate dehydrogenase found in the cytoplasm and peroxisomes. It contains the PTS-1 peroxisomal targeting signal sequence. The presence of this enzyme in peroxisomes suggests roles in the regeneration of NADPH for intraperoxisomal reductions, such as the conversion of 2, 4-dienoyl-CoAs to 3-enoyl-CoAs, as well as in peroxisomal reactions that consume 2-oxoglutarate, namely the alpha-hydroxylation of phytanic acid. The cytoplasmic enzyme serves a significant role in cytoplasmic NADPH production. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Sep 2013]
Gene Info
Gene Group
Isocitrate dehydrogenases
Locus Type
gene with protein product
Location
2q34
Ensembl
ENSG00000138413
Associated Conditions (18)
Paroxysmal extreme pain disorder
Enchondromatosis
Acute myeloid leukemia
Maffucci syndrome
Glioma susceptibility 1
Neoplasm
Juvenile type testicular granulosa cell tumor
Medulloblastoma
Cholangiocarcinoma
Hepatocellular carcinoma
Medulloblastoma SHH activated
Glioblastoma multiforme
somatic
Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
Metaphyseal chondromatosis
Acute myeloid leukemia with NPM1 somatic mutations
Astrocytoma IDH-mutant
Oligodendroglioma
Key Variants
All Variants (4)
RSID Category Clinical Significance Conditions
RS2124849065 Health Risk Likely pathogenic Paroxysmal extreme pain disorder, Paroxysmal extreme pain disorder
RS62193615 Health Risk Likely pathogenic Enchondromatosis, Enchondromatosis
RS121913499 Health Risk Pathogenic Acute myeloid leukemia, Enchondromatosis, Maffucci syndrome
RS121913500 Health Risk Pathogenic Glioblastoma multiforme, somatic, Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria
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