Gene entry
CP
ceruloplasmin
- Chromosome
- 3
- Cytoband
- 3q24-q25.1
- Variants (rsID)
- 27
CP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q24-q25.1). Its official name is “ceruloplasmin”. The reference table lists 27 variants (rsID) for this gene.
Clinically classified variants
13 reference-table entries with clinical significance.
- rs1053709Benignsingle nucleotide variantDeficiency of ferroxidase
- rs115552500Benignsingle nucleotide variantDeficiency of ferroxidase
- rs56033670Benignsingle nucleotide variantDeficiency of ferroxidase
- rs73866999Benignsingle nucleotide variantDeficiency of ferroxidase
- rs13098532Conflicting interpretationssingle nucleotide variantDeficiency of ferroxidase|Hermansky-Pudlak syndrome 3
- rs34386552Conflicting interpretationssingle nucleotide variantDeficiency of ferroxidase
- rs386134124Pathogenicsingle nucleotide variantDeficiency of ferroxidase
- rs150303869Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
- rs187293972Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
- rs200156117Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
- rs200683433Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
- rs200864206Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
- rs386134123Uncertain significancesingle nucleotide variantDeficiency of ferroxidase
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.