| IDH2 |
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| Identifiers |
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| Aliases | IDH2, D2HGA2, ICD-M, IDH, IDHM, IDP, IDPM, mNADP-IDH, isocitrate dehydrogenase (NADP(+)) 2, mitochondrial, isocitrate dehydrogenase (NADP(+)) 2, IDH-2 |
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| External IDs | OMIM: 147650; MGI: 96414; HomoloGene: 37590; GeneCards: IDH2; OMA:IDH2 - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 7 (mouse) |
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| | Band | 7 D2|7 45.43 cM | Start | 79,744,594 bp |
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| End | 79,765,140 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - apex of heart
- gastrocnemius muscle
- muscle of thigh
- body of tongue
- vastus lateralis muscle
- triceps brachii muscle
- left ventricle
- skeletal muscle tissue
- glutes
- Skeletal muscle tissue of biceps brachii
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| | Top expressed in | - right ventricle
- right kidney
- myocardium of ventricle
- cardiac muscle tissue of left ventricle
- atrium
- plantaris muscle
- soleus muscle
- atrioventricular valve
- thoracic diaphragm
- otic vesicle
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Isocitrate dehydrogenase [NADP], mitochondrial is an enzyme that in humans is encoded by the IDH2 gene.
Isocitrate dehydrogenases are enzymes that 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 the IDH2 gene is the NADP(+)-dependent isocitrate dehydrogenase found in the mitochondria. It plays a role in intermediary metabolism and energy production. This protein may tightly associate or interact with the pyruvate dehydrogenase complex. Somatic mosaic mutations of this gene have also been found associated to Ollier disease and Maffucci syndrome.