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Gene : CP Homo sapiens

Name  ? ceruloplasmin Cytological Location  3q24-q25.1
Brief Description  ceruloplasmin
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]
  • synonyms:
  • uc003ewy.6,
  • OTTHUMG00000159563,
  • ceruloplasmin (ferroxidase),
  • ferroxidase,
  • CP-2,
  • HGNC:2295,
  • NM_000096,
  • CP,
  • M13536
  • identifiers:
  • 1356,
  • ENSG00000047457,
  • CP

Genome feature

Region: gene ? Length: 59599  
Location: 3:149162410-149222008 reverse strand Cyto location: 3q24-q25.1

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Gene -> HPO annotation (Human Phenotype Ontology)

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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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596 SNPs

5 Cross References

18 Data Sets

10 Homologues

0 Located Features

97 Rna Seq Results