GYG1

Description		glycogenin 1
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GO Annotations	Cellular Component	Extracellular Region Cytosol Membrane Secretory Granule Lumen Lysosomal Lumen Ficolin-1-rich Granule Lumen
	Molecular Function	Protein Binding Glycogenin Glucosyltransferase Activity Transferase Activity, Transferring Glycosyl Groups Manganese Ion Binding Protein Homodimerization Activity UDP-alpha-D-glucose:glucosyl-glycogenin Alpha-D-glucosyltransferase Activity
	Biological Process	Glycogen Biosynthetic Process Neutrophil Degranulation
Pathways		Glycogen synthesis Myoclonic epilepsy of Lafora Glycogen storage disease type XV (GYG1) Glycogen storage disease type 0 (muscle GYS1) Glycogen storage disease type II (GAA) Neutrophil degranulation Glycogen breakdown (glycogenolysis) Glycogen breakdown (glycogenolysis)
Drugs		Uridine diphosphate glucose Uridine-5'-Diphosphate
Diseases
GWAS		Diverticular disease ( 30177863)
Interacting Genes		7 interacting genes: C1QTNF9 CD6 CMSS1 GYG2 GYS1 POM121 TRIM7
Entrez ID		2992
HPRD ID		06805
Ensembl ID		ENSG00000163754
Uniprot IDs		P46976
PDB IDs		3Q4S 3QVB 3RMV 3RMW 3T7M 3T7N 3T7O 3U2T 3U2U 3U2V 3U2W 3U2X 6EQJ 6EQL
Enriched GO Terms of Interacting Partners?
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