AMN and TECPR2

		AMN	TECPR2
Description		amnion associated transmembrane protein	tectonin beta-propeller repeat containing 2
Image			No pdb structure
GO Annotations	Cellular Component	Extracellular Space Plasma Membrane Clathrin-coated Pit Endosome Membrane Integral Component Of Membrane Apical Plasma Membrane Endocytic Vesicle Brush Border Membrane Protein-containing Complex Extracellular Exosome	Cytoplasm
	Molecular Function	Signaling Receptor Binding Protein Binding	Protein Binding
	Biological Process	Receptor-mediated Endocytosis Excretion Protein Localization Cobalamin Transport Golgi To Plasma Membrane Protein Transport	Autophagy Protein Exit From Endoplasmic Reticulum
Pathways		Cobalamin (Cbl, vitamin B12) transport and metabolism Defective AMN causes hereditary megaloblastic anemia 1 Defective CUBN causes hereditary megaloblastic anemia 1 HDL clearance
Drugs		Hydroxocobalamin
Diseases
GWAS		Body mass index ( 26426971)	Birdshot chorioretinopathy ( 24957906) Blood protein levels ( 28240269) Body mass index ( 26426971) Platelet count ( 27863252) Refractive error ( 32231278)
Interacting Genes		4 interacting genes: CDC42BPB MTA1 STAMBP TECPR2	2 interacting genes: AMN CCR2
Entrez ID		81693	9895
HPRD ID		09314	17184
Ensembl ID		ENSG00000166126	ENSG00000196663
Uniprot IDs		B3KP64 Q9BXJ7	O15040
PDB IDs		6GJE
Enriched GO Terms of Interacting Partners?
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