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Ceruloplasmin encodes a protein that is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe(II)transferrin to Fe(III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities.
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Protein Aliases: Ceruloplasmin; Cuproxidase ceruloplasmin; Ferroxidase ceruloplasmin; Glutathione peroxidase ceruloplasmin; Glutathione-dependent peroxiredoxin ceruloplasmin
Gene Aliases: CP; CP-2
UniProt ID: (Human) P00450
Entrez Gene ID: (Human) 1356
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