CP

Description		ceruloplasmin
Image
GO Annotations	Cellular Component	Extracellular Region Extracellular Space Cell Lysosomal Membrane Endoplasmic Reticulum Lumen Plasma Membrane Extracellular Exosome Blood Microparticle
	Molecular Function	Ferroxidase Activity Copper Ion Binding Oxidoreductase Activity Chaperone Binding
	Biological Process	Copper Ion Transport Iron Ion Transport Cellular Iron Ion Homeostasis Post-translational Protein Modification Cellular Protein Metabolic Process Iron Ion Homeostasis Oxidation-reduction Process
Pathways		Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) Metal ion SLC transporters Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages) Defective CP causes aceruloplasminemia (ACERULOP) Post-translational protein phosphorylation Iron uptake and transport
Drugs		Drotrecogin alfa Calcium Iron Zinc
Diseases
GWAS		Subcutaneous adipose tissue ( 22589738)
Interacting Genes		7 interacting genes: ATP7A BTRC GAST LTF MPO PLG PROC
Entrez ID		1356
HPRD ID		00317
Ensembl ID		ENSG00000047457
Uniprot IDs		A5PL27 P00450
PDB IDs		1KCW 2J5W 4EJX 4ENZ
Enriched GO Terms of Interacting Partners?
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