The protein encoded by this gene belongs to the HMG-CoA synthase family. It is a mitochondrial enzyme that catalyzes the first reaction of ketogenesis, a metabolic pathway that provides lipid-derived energy for various organs during times of carbohydrate deprivation, such as fasting. Mutations in this gene are associated with HMG-CoA synthase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HMGCS2-20-RE | 20 (40 μL) | 200 μL |  |
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| HMGCS2-20-OR | 20 (40 μL) | 200 μL |  |
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| HMGCS2-20-GO | 20 (40 μL) | 200 μL |  |
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| HMGCS2-20-GR | 20 (40 μL) | 200 μL |  |
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| HMGCS2-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene belongs to the HMG-CoA synthase family. It is a mitochondrial enzyme that catalyzes the first reaction of ketogenesis, a metabolic pathway that provides lipid-derived energy for various organs during times of carbohydrate deprivation, such as fasting. Mutations in this gene are associated with HMG-CoA synthase deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
Gene Symbol : HMGCS2
Gene Name : 3-hydroxy-3-methylglutaryl-CoA synthase 2
Chromosome : CHR 1: 119,769,124-119,747,995
Locus : 1p12
Alt. Genes : AKAP9
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