KATNBL1 and GYS1

Data Source:
BioGRID (two hybrid)

		KATNBL1	GYS1
Description		katanin regulatory subunit B1 like 1	glycogen synthase 1
Image		No pdb structure	No pdb structure
GO Annotations	Cellular Component	Nucleus Nucleoplasm Nucleolus Cytoplasm Midbody Cleavage Furrow Mitotic Spindle Mitotic Spindle Pole	Cytoplasm Cytosol Membrane Inclusion Body
	Molecular Function	Protein Binding Microtubule Binding	Glycogen (starch) Synthase Activity Protein Binding Glucose Binding Protein Kinase Binding Glycogen Synthase Activity, Transferring Glucose-1-phosphate
	Biological Process	Positive Regulation Of Cytoskeleton Organization	Glycogen Biosynthetic Process Heart Development
Pathways			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		39 interacting genes: CA12 CDC37 CLIC3 CPNE2 FRS3 GEM GPANK1 GUCD1 GYS1 HAP1 KAT7 KATNAL1 LMO4 LONRF1 MFAP1 MYO15B NEK6 NTAQ1 NXF1 OSGIN1 PDPK1 PFKFB1 PIBF1 POLR3C PRKAB2 PSMB1 RAD51D SCNM1 SDCBP SMARCD1 SNAPC3 TCEANC TRIM41 TUT1 ZC2HC1C ZNF329 ZNF417 ZNF572 ZNF587	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		79768	2997
HPRD ID		07995	00721
Ensembl ID		ENSG00000134152	ENSG00000104812
Uniprot IDs		A0A024R9P5 Q9H079	P13807
PDB IDs
Enriched GO Terms of Interacting Partners?
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