Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| AMPD1-20-RE | 20 (40 μL) | 200 μL |  |
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| AMPD1-20-OR | 20 (40 μL) | 200 μL |  |
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| AMPD1-20-GO | 20 (40 μL) | 200 μL |  |
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| AMPD1-20-GR | 20 (40 μL) | 200 μL |  |
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| AMPD1-20-AQ | 20 (40 μL) | 200 μL |  |
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Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
Gene Symbol : AMPD1
Gene Name : Adenosine monophosphate deaminase 1
Chromosome : CHR 1: 114,695,617-114,673,097
Locus : 1p13.2
Alt. Genes : SGK2
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