Selected-GenAtlas references SOURCE GeneCards NCBI Gene Swiss-Prot Orphanet Ensembl
HGNC UniGene Nucleotide OMIM UCSC
Home Page
FLASH GENE
Symbol CP contributors: mct - updated : 29-11-2019
HGNC name ceruloplasmin (ferroxidase)
HGNC id 2295
ASSOCIATED DISORDERS
corresponding disease(s) CP
Other morbid association(s)
TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
constitutional   deletion    
of hephaestin and ceruloplasmin induces a serious systemic iron deficiency and disrupts iron homeostasis
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS