The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GYS1BA-20-REGO | 20 (40 μL) | 200 μL |
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| GYS1BA-20-REGR | 20 (40 μL) | 200 μL |
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| GYS1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| GYS1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| GYS1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| GYS1BA-20-GROR | 20 (40 μL) | 200 μL |
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| GYS1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| GYS1BA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
Gene Symbol : GYS1
Gene Name : Glycogen synthase 1
Chromosome : CHR 19: 489,933,52-489,681,24
Locus : 19q13.33
Alt. Genes : RBM12
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