PLEKHF2 and TCN2

		PLEKHF2	TCN2
Description		pleckstrin homology and FYVE domain containing 2	transcobalamin 2
Image		No pdb structure
GO Annotations	Cellular Component	Endoplasmic Reticulum Transport Vesicle Early Endosome Membrane	Extracellular Region Extracellular Space Endosome Lysosomal Lumen
	Molecular Function	Protein Binding Phosphatidylinositol Binding Metal Ion Binding	Protein Binding Cobalamin Binding Metal Ion Binding
	Biological Process	Protein Transport	Cobalt Ion Transport Cobalamin Metabolic Process Cobalamin Transport
Pathways			Cobalamin (Cbl, vitamin B12) transport and metabolism Defective TCN2 causes hereditary megaloblastic anemia Defective CD320 causes methylmalonic aciduria
Drugs
Diseases
GWAS		Radiation response ( 20923822)	Blood protein levels ( 30072576 29875488) Factor VIII levels ( 30586737) Moyamoya disease ( 29273593) Venous thromboembolism ( 31420334) vWF levels ( 30586737)
Interacting Genes		71 interacting genes: ACY3 AIDA AIMP2 APP APPL1 ARL14EP BEND7 BLOC1S6 BSCL2 CAVIN2 CCDC172 CCDC85B CEP44 CGGBP1 CHIC2 DPPA4 DRAP1 DTX2 DUT ESRP1 FBXO28 FHL3 FOXA1 FRMD8 GFER GLUL GNMT GPBP1 GPBP1L1 HEY1 HSPB7 L3MBTL3 LDOC1 MAX MBIP MEAF6 NKG7 NONO NPM2 PDP1 PEX2 PRDM14 PRKAR1A PRPSAP1 RAB39A RABAC1 RADX RSPO2 RTN1 RTN3 RTN4 S100A1 S100A13 SEPTIN2 SEPTIN5 SEPTIN6 SETBP1 SFN SPEF1 TBX3 TCN2 TNFAIP8 TRAF6 TRAPPC3 TSC22D3 TXNL4B UBE2Z USF1 ZNF250 ZNF263 ZNF398	5 interacting genes: APP CBL PAXIP1 PLEKHF2 RHOU
Entrez ID		79666	6948
HPRD ID		15147	02037
Ensembl ID		ENSG00000175895	ENSG00000185339
Uniprot IDs		Q9H8W4	P20062
PDB IDs			2BB5 4ZRP 4ZRQ 5NO0 5NP4 5NRP 5NSA
Enriched GO Terms of Interacting Partners?
Tagcloud ?
Tagcloud (Difference) ?
Tagcloud (Intersection) ?