Gene

cp

ID

ZDB-GENE-010522-1

Name

ceruloplasmin

Symbol

cp Nomenclature History

Previous Names

cer (1)
wu:fi23f10 (1)

Type

protein_coding_gene

Location

Chr: 22 Mapping Details/Browsers

Description

Predicted to have ferroxidase activity. Predicted to be involved in iron ion homeostasis and iron ion transport. Localizes to cytoplasm and nucleus. Human ortholog(s) of this gene implicated in aceruloplasminemia; epilepsy; and hemosiderosis. Is expressed in digestive system; female organism; liver and biliary system; male organism; and yolk syncytial layer. Orthologous to human CP (ceruloplasmin).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

96 figures from 62 publications

Cross-Species Comparison

High Throughput Data

GEO (1)

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

Thisse Expression Data

MGC:55445 (8 images)

Wild Type Expression Summary

Phenotype

All Phenotype Data: 1 Figure from Choksi et al., 2014
Cross-Species Comparison: Alliance

Phenotype Summary

Mutations

Mutants

Sequence Targeting Reagents

Human Disease

Associated With cp Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
aceruloplasminemia	Alliance	Aceruloplasminemia	604290

Associated With cp Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Binding_site	IPR002355	Multicopper oxidase, copper-binding site
Conserved_site	IPR033138	Multicopper oxidases, conserved site
Domain	IPR011706	Multicopper oxidase, C-terminal
Domain	IPR011707	Multicopper oxidase-like, N-terminal
Domain	IPR048236	Ceruloplasmin-like, fifth cupredoxin domain
Family	IPR050633	Neuropilin/Multicopper Oxidase/Coagulation Factor
Homologous_superfamily	IPR008972	Cupredoxin