This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| PYGM-20-RE | 20 (40 μL) | 200 μL |  |
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| PYGM-20-OR | 20 (40 μL) | 200 μL |  |
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| PYGM-20-GO | 20 (40 μL) | 200 μL |  |
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| PYGM-20-GR | 20 (40 μL) | 200 μL |  |
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| PYGM-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009]
Gene Symbol : PYGM
Gene Name : Glycogen phosphorylase, muscle associated
Chromosome : CHR 11: 647,607,14-647,463,88
Locus : 11q13.1
Alt. Genes : FARP1
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