ZNF552 and GYS1

Data Source:
BioGRID (two hybrid)

		ZNF552	GYS1
Description		zinc finger protein 552	glycogen synthase 1
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleus	Cytoplasm Cytosol Membrane Inclusion Body
	Molecular Function	RNA Polymerase II Cis-regulatory Region Sequence-specific DNA Binding DNA-binding Transcription Factor Activity, RNA Polymerase II-specific Protein Binding Metal Ion Binding	Glycogen (starch) Synthase Activity Protein Binding Glucose Binding Protein Kinase Binding Glycogen Synthase Activity, Transferring Glucose-1-phosphate
	Biological Process	Regulation Of Transcription By RNA Polymerase II	Glycogen Biosynthetic Process Heart Development
Pathways		Generic Transcription Pathway	Glycogen synthesis Myoclonic epilepsy of Lafora Glycogen storage disease type XV (GYG1) Glycogen storage disease type 0 (muscle GYS1)
Drugs
Diseases			Glycogen storage diseases (GSD), including: von Gierke disease (GSD type Ia); Pompe disease (GSD type II); Cori disease, Forbe disease (GSD type III); Andersen disease (GSD type IV); McArdle disease (GSD type V); Hers disease (GSD type VI); Tarui disease (GSD type VII); Phosphorylase kinase deficiency (GSD type IX); Fanconi-Bickel syndrome (GSD type XI); Glycogen synthase deficiency (GSD type 0)
GWAS
Interacting Genes		33 interacting genes: ANKRD11 AP1M1 CARD10 CCDC125 CCDC57 CCNDBP1 CIB3 CTNNA3 CYSRT1 DVL3 FRS3 GEM GOLGA6L9 GYS1 HOXB5 INO80B KCTD7 KRTAP4-11 KRTAP4-5 LNX1 MID2 PHF24 SCNM1 TEKT4 TP53BP2 TRIM41 ZBTB16 ZNF648 ZNF655 ZNF792 ZNF835 ZNF837 ZRANB1	43 interacting genes: AIMP2 APP BEND7 CCDC33 CDCA8 CLVS2 CRX CSNK2A1 EFHC2 FAM228A GSK3B GYG1 GYG2 HOXB6 HOXC8 IHO1 INCA1 KATNBL1 KLF1 KLF4 MAPKAPK5 MEOX1 NDUFB7 NHLRC1 PCYT1A PINX1 PLAGL2 PNMA5 PRKACA RBM48 SNIP1 SORBS3 SUMO2 TFAP2D TLE5 WASHC1 ZBTB33 ZNF212 ZNF326 ZNF474 ZNF552 ZNF620 ZNF774
Entrez ID		79818	2997
HPRD ID		15835	00721
Ensembl ID		ENSG00000178935	ENSG00000104812
Uniprot IDs		B7Z1H1 Q9H707	P13807
PDB IDs
Enriched GO Terms of Interacting Partners?
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