NP_001155059.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
NCBI Official Full Name
glycogen
NCBI Official Synonym Full Names
glycogen synthase 1
NCBI Official Synonym Symbols
NCBI Protein Information
glycogen [starch] synthase, muscle
UniProt Protein Name
Glycogen [starch] synthase, muscle
UniProt Synonym Gene Names
NCBI Summary for GYS1
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]
UniProt Comments for GYS1
GYS1: muscle glycogen synthase 1. Transfers glucosyl residue from UDP-glucose to glycogen. Regulated allosterically by glucose-6-phosphate, and by PKA-mediated phosphorylation.
Protein type: Carbohydrate Metabolism - starch and sucrose; EC 2.4.1.11; Transferase
Chromosomal Location of Human Ortholog: 19q13.33
Cellular Component: cytosol; inclusion body; membrane
Molecular Function: glucose binding; glycogen (starch) synthase activity; protein binding; protein kinase binding
Biological Process: glycogen biosynthetic process; heart development
Disease: Glycogen Storage Disease 0, Muscle
Research Articles on GYS1
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Products associated with GYS1 elisa kit
Pathways associated with GYS1 elisa kit
Diseases associated with GYS1 elisa kit
Organs/Tissues associated with GYS1 elisa kit
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