Entity Details

Primary name CP
Entity type gene
Source Source Link

Details

PrimaryID1356
RefseqGeneNG_011800
SymbolCP
Nameceruloplasmin
Chromosome3
Location3q24-q25.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1993-05-05
ModificationDate2021-06-20

Ontological Relatives

UniProt IDsCERU_HUMAN

GO terms

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GOName
GO:0004322 ferroxidase activity
GO:0005507 copper ion binding
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005765 lysosomal membrane
GO:0005788 endoplasmic reticulum lumen
GO:0005886 plasma membrane
GO:0006825 copper ion transport
GO:0006826 iron ion transport
GO:0006879 cellular iron ion homeostasis
GO:0016491 oxidoreductase activity
GO:0043687 post-translational protein modification
GO:0044267 cellular protein metabolic process
GO:0051087 chaperone binding
GO:0055072 iron ion homeostasis
GO:0070062 extracellular exosome
GO:0072562 blood microparticle

Diseases

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Disease IDSourceNameDescription
604290 OMIMAceruloplasminemia (ACERULOP)An autosomal recessive disorder of iron metabolism characterized by iron accumulation in the brain as well as visceral organs. Clinical features consist of the triad of retinal degeneration, diabetes mellitus and neurological disturbances. The disease is caused by variants affecting the gene represented in this entry.