The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content. [provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| GYS2BA-20-REGO | 20 (40 μL) | 200 μL |
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| GYS2BA-20-REGR | 20 (40 μL) | 200 μL |
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| GYS2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| GYS2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| GYS2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| GYS2BA-20-GROR | 20 (40 μL) | 200 μL |
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| GYS2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| GYS2BA-20-AQOR | 20 (40 μL) | 200 μL |
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The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content. [provided by RefSeq, Dec 2009]
Gene Symbol : GYS2
Gene Name : Glycogen synthase 2
Chromosome : CHR 12: 216,048,57-215,361,88
Locus : 12p12.1
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