Basic Information

CRP

Full name: C-reactive protein

Gene type: protein coding

HGNC ID: HGNC:2367

Gene location: 1q23.2

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/1401

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:2367

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_000567.3

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P02741

AlphaFold: https://alphafold.ebi.ac.uk/entry/P02741

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/123260

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=1401

Pathway resources

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
CRP nAMD respond to PDT N/A rs2808635 G>C / G>T chr1:159724419 (GRCh38.p13)
CRP nAMD respond to PDT N/A rs876538 T>A / T>C / T>G chr1:159705927 (GRCh38.p13)
CRP nAMD respond to PDT N/A rs3093077 A>C / A>G / A>T chr1:159709846 (GRCh38.p13)
CRP nAMD respond to PDT N/A rs1572970 G>A / G>C chr1:159703795 (GRCh38.p13)
CRP nAMD respond to PDT N/A rs876537 C>T chr1:159705143 (GRCh38.p13)
CRP nAMD respond to PDT 3 Prime UTR Variant rs1205 C>T chr1:159712443 (GRCh38.p13)
CRP nAMD respond to PDT Synonymous Variant rs1800947 C>A / C>G / C>T chr1:159713648 (GRCh38.p13)
CRP nAMD respond to PDT Intron Variant rs1130864 G>A chr1:159713301 (GRCh38.p13)
CRP nAMD respond to PDT Intron Variant rs1417938 T>A / T>C chr1:159714396 (GRCh38.p13)