| 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.