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 |
---|---|---|---|---|
GYS2-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
GYS2-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
GYS2-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
GYS2-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
GYS2-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
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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