OGDH Chromosome 7

Oxoglutarate dehydrogenase
7 variants 7 Health Risk

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What This Gene Does
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 Info
Gene Group
"Oxoglutarate dehydrogenase family|Oxoglutarate dehydrogenase complex subunits"
Locus Type
gene with protein product
Location
7p13
Ensembl
ENSG00000105953
Associated Conditions (2)
Oxoglutaricaciduria
OGDH-related disorder
Key Variants
All Variants (7)
RSID Category Clinical Significance Conditions
RS113587743 Health Risk Conflicting classifications of pathogenicity Oxoglutaricaciduria, Oxoglutaricaciduria
RS151001666 Health Risk Conflicting classifications of pathogenicity Oxoglutaricaciduria, OGDH-related disorder, Oxoglutaricaciduria
RS1788472672 Health Risk Conflicting classifications of pathogenicity Oxoglutaricaciduria, Oxoglutaricaciduria
RS2116155540 Health Risk Pathogenic Oxoglutaricaciduria, Oxoglutaricaciduria
RS2116163953 Health Risk Pathogenic Oxoglutaricaciduria, Oxoglutaricaciduria
RS2484805251 Health Risk Pathogenic Oxoglutaricaciduria, Oxoglutaricaciduria
RS2484850454 Health Risk Pathogenic Oxoglutaricaciduria, Oxoglutaricaciduria
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