This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| HGD-20-RE | 20 (40 μL) | 200 μL |  |
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| HGD-20-OR | 20 (40 μL) | 200 μL |  |
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| HGD-20-GO | 20 (40 μL) | 200 μL |  |
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| HGD-20-GR | 20 (40 μL) | 200 μL |  |
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| HGD-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes the enzyme homogentisate 1,2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.[provided by RefSeq, May 2010]
Gene Symbol : HGD
Gene Name : Homogentisate 1,2-dioxygenase
Chromosome : CHR 3: 120,682,570-120,628,167
Locus : 3q13.33
Alt. Genes : PREB
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