GNE and KRTAP11-1

Data Source:
BioGRID (two hybrid)

		GNE	KRTAP11-1
Description		glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	keratin associated protein 11-1
Image			No pdb structure
GO Annotations	Cellular Component	Cytoplasm Cytosol	Cytosol Intermediate Filament
	Molecular Function	Hydrolase Activity, Hydrolyzing O-glycosyl Compounds Protein Binding ATP Binding UDP-N-acetylglucosamine 2-epimerase Activity N-acylmannosamine Kinase Activity Metal Ion Binding	Protein Binding
	Biological Process	N-acetylglucosamine Biosynthetic Process UDP-N-acetylglucosamine Metabolic Process N-acetylneuraminate Metabolic Process Cell Adhesion Carbohydrate Phosphorylation	Keratinization
Pathways		Sialic acid metabolism Defective GNE causes sialuria, Nonaka myopathy and inclusion body myopathy 2	Keratinization
Drugs
Diseases		Distal muscular dystrophies, including: Welander distal myopathy (WDM); Tibial muscular dystrophy (TMD); Nonaka distal myopathy with rimmed vacuoles (DMRV); Miyoshi myopathy (MM); Laing myopathy (MPD1); Distal nebulin myopathy (DNM); Distal desminopathy (MFM1); alpha-B Crystallinopathy (MFM2); Distal myotilinopathy (MFM3); Distal zaspopathy (MFM4); Distal myopathy 3 (MPD2, VCPDM) Nonaka distal myopathy (NM); Distal myopathy with rimmed vacuoles (DMRV); Hereditary inclusion body myopathy (hIBM) Sialuria/ Sialic acid storage disease, including: Infantile sialic acid storage disease (ISSD); Sialuria, Finnish type / Salla disease (SD); Sialuria, French type
GWAS		Bipolar disorder (inflammation and infection response interaction) ( 25781172) Bisphosphonate-associated atypical femoral fracture ( 31006051)	Height ( 28552196)
Interacting Genes		65 interacting genes: ADAMTSL4 C22orf39 CFP CRMP1 CYSRT1 ECM1 EGFL7 GRN GTPBP3 HOXA1 KIAA1549 KPRP KRT31 KRT34 KRT40 KRT83 KRT85 KRT86 KRTAP1-1 KRTAP1-3 KRTAP10-3 KRTAP10-5 KRTAP10-7 KRTAP10-8 KRTAP10-9 KRTAP11-1 KRTAP12-3 KRTAP13-2 KRTAP13-3 KRTAP17-1 KRTAP19-2 KRTAP19-7 KRTAP3-1 KRTAP3-3 KRTAP4-1 KRTAP4-11 KRTAP4-12 KRTAP4-4 KRTAP5-9 KRTAP6-1 KRTAP6-2 KRTAP6-3 KRTAP9-2 KRTAP9-3 KRTAP9-8 MDFI MGAT5B NBPF19 NID2 NOTCH2NLA PLA2G10 PRICKLE4 RIF1 SPRY1 SPRY2 SPRY3 SSC4D TRIM27 TRIM42 TRIP6 TSPAN4 VWC2 WDR83 WWOX ZBTB16	104 interacting genes: AGR3 ANAPC11 ANKS1A ASB13 ATG9A ATXN1L BEX2 CERK CFP CHERP CRYBA1 CRYBA2 CSKMT CYSRT1 DHRS1 DTX2 DUSP21 EFEMP2 ENKD1 ETFDH FAM222B FANCL FASLG FBLN1 FNDC3B FOXH1 FRS3 GATA2 GNE GPS2 GPSM3 GRN HEY2 HOXA1 HOXC8 HR KLHL38 KRT83 KRTAP10-5 KRTAP10-8 KRTAP12-1 KRTAP12-3 KRTAP12-4 KRTAP13-2 KRTAP15-1 KRTAP26-1 KRTAP4-11 KRTAP4-2 KRTAP5-11 KRTAP5-3 KRTAP5-4 KRTAP5-6 KRTAP5-9 KRTAP6-1 KRTAP6-2 KRTAP6-3 KRTAP9-2 KRTAP9-3 KRTAP9-8 LCE1A LCE1B LCE1F LCE2A LCE3A LCE3C LGALS4 LIMS3 LIMS4 LMO4 MEIS2 MICOS10-NBL1 NBL1 NUFIP2 OIT3 OLIG3 OR7A17 OTX1 PCSK5 PLA2G10 PLSCR3 RBPMS RBPMS2 RNF38 SLC13A5 SNRPC SPAG8 SPRY1 STK16 TBX6 TEKT4 TENT5D TFAP2D TLE5 TLX3 TNS2 TRIM54 VASN VENTX VGLL3 VWC2L WWOX YIPF3 ZDHHC17 ZIC1
Entrez ID		10020	337880
HPRD ID		04825	11196
Ensembl ID		ENSG00000159921	ENSG00000182591
Uniprot IDs		Q9Y223	Q8IUC1
PDB IDs		2YHW 2YHY 2YI1 3EO3 4ZHT
Enriched GO Terms of Interacting Partners?
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