Short Description: The protein encoded by this gene 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. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012]. More information related to gene Ceruloplasmin.
Synonyms and alternative names related to Ceruloplasmin
ceruloplasmin (CP)
ceruloplasmin (cp)
ceruloplasmin (Cp)
ceruloplasmin (LOC100533122)
CERP
CP
CP-2
D3Ertd555e
fi23f10
wu:fi23f10
Gene-IDs for different species
Protein level used designations for Ceruloplasmin
ceruloplasmin
ferroxidase
hypothetical protein
ceruloplasmin (ferroxidase)
Proteomics products related to Ceruloplasmin Gene
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