AMN

Description		amnion associated transmembrane protein
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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
	Molecular Function	Signaling Receptor Binding Protein Binding
	Biological Process	Receptor-mediated Endocytosis Multicellular Organism Development Excretion Protein Localization Cobalamin Metabolic Process Cobalamin Transport High-density Lipoprotein Particle Clearance Golgi To Plasma Membrane Protein Transport
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)
Novel Interacting Genes		3 novel interacting genes: CDC42BPB MTA1 TECPR2
Interacting Genes		1 interacting genes: STAMBP
Entrez ID		81693
HPRD ID		09314
Ensembl ID		ENSG00000166126
Uniprot IDs		B3KP64 Q9BXJ7
PDB IDs		6GJE
Enriched GO Terms of Interacting Partners?
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