CP - Gene browser

CP

ceruloplasmin

HCNC Approved Symbol: CP (HGNC:2295)
Genomic Coordinates: 3:149,162,414 - 149,221,829 (3q24-q25.1)
Synonyms: AB073614
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the CP gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results