This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
OGDH-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
OGDH-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
OGDH-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
OGDH-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
OGDH-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]
Gene Symbol : OGDH
Gene Name : Oxoglutarate dehydrogenase
Chromosome : CHR 7: 446,065,21-447,090,69
Locus : 7p13
Alt. Genes : HIPK3
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