This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria and Charcot-Marie-Tooth Disease Type 2Q. [provided by RefSeq, May 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DHTKD1-20-RE | 20 (40 μL) | 200 μL |  |
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| DHTKD1-20-OR | 20 (40 μL) | 200 μL |  |
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| DHTKD1-20-GO | 20 (40 μL) | 200 μL |  |
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| DHTKD1-20-GR | 20 (40 μL) | 200 μL |  |
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| DHTKD1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria and Charcot-Marie-Tooth Disease Type 2Q. [provided by RefSeq, May 2013]
Gene Symbol : DHTKD1
Gene Name : Dehydrogenase E1 and transketolase domain containing 1
Chromosome : CHR 10: 120,689,16-121,232,27
Locus : 10p14
Alt. Genes : ENAM
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