Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3579
Gene name Gene Name - the full gene name approved by the HGNC.
C-X-C motif chemokine receptor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CXCR2
Synonyms (NCBI Gene) Gene synonyms aliases
CD182, CDw128b, CMKAR2, IL8R2, IL8RA, IL8RB, WHIMS2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
WHIMS2
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q35
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the G-protein-coupled receptor family. This protein is a receptor for interleukin 8 (IL8). It binds to IL8 with high affinity, and transduces the signal through a G-protein activated second messenger system.
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1574542732 A>T Likely-pathogenic Coding sequence variant, stop gained
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017358 hsa-miR-335-5p Microarray 18185580
MIRT647735 hsa-miR-4524b-3p HITS-CLIP 23824327
MIRT647734 hsa-miR-4293 HITS-CLIP 23824327
MIRT647727 hsa-miR-411-5p HITS-CLIP 23824327
MIRT647733 hsa-miR-6823-5p HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
CEBPA Unknown 18555777
NFKB1 Activation 19156404
NFKB1 Unknown 18555777
RELA Activation 19156404
RELA Unknown 18555777
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002407 Process Dendritic cell chemotaxis TAS 16621978
GO:0004918 Function Interleukin-8 receptor activity IDA 10820279
GO:0004930 Function G protein-coupled receptor activity IDA 10438939
GO:0005515 Function Protein binding IPI 17435771, 21876773, 22904195, 23597562, 32296183
GO:0005654 Component Nucleoplasm IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
146928 6027 ENSG00000180871
Protein
UniProt ID P25025
Protein name C-X-C chemokine receptor type 2 (CXC-R2) (CXCR-2) (CDw128b) (GRO/MGSA receptor) (High affinity interleukin-8 receptor B) (IL-8R B) (IL-8 receptor type 2) (CD antigen CD182)
Protein function Receptor for interleukin-8 which is a powerful neutrophil chemotactic factor (PubMed:1891716). Binding of IL-8 to the receptor causes activation of neutrophils. This response is mediated via a G-protein that activates a phosphatidylinositol-calc
PDB 4Q3H , 5TYT , 6KVA , 6KVF , 6LFM , 6LFO , 8XVU , 8XWA , 8XWF , 8XWM , 8XWN , 8XWS , 8XWV , 8XX3 , 8XX6 , 8XX7 , 8XXH , 8XXR , 8XXX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 65 314 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 360
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Cytokine-cytokine receptor interaction
Viral protein interaction with cytokine and cytokine receptor
Chemokine signaling pathway
Phospholipase D signaling pathway
Endocytosis
Epithelial cell signaling in Helicobacter pylori infection
Human cytomegalovirus infection
  Chemokine receptors bind chemokines
G alpha (i) signalling events
Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Juvenile arthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 19565504
Congenital neutropenia Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency rs118203968, rs118203969, rs118203970, rs118203971, rs267606834, rs28936381, rs137854447, rs137854448, rs137854450, rs28931611, rs137854451, rs200478425, rs587777730, rs606231474, rs606231475
View all (30 more)
Hypertension Hypertensive disease rs13306026 27678262
Unknown
Disease term Disease name Evidence References Source
Congenital Neutropenia autosomal recessive severe congenital neutropenia due to CXCR2 deficiency GenCC
Ulcerative colitis Ulcerative colitis GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Crohn Disease Crohn Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acquired Immunodeficiency Syndrome Associate 17360650
Acute On Chronic Liver Failure Inhibit 27974825
Adenocarcinoma Associate 25485576, 33935122, 35212311
Adenocarcinoma of Lung Inhibit 35768814
Adenomyosis Associate 16500343
Alzheimer Disease Associate 33804025
Aortic Aneurysm Abdominal Stimulate 16308497
Appendicitis Stimulate 27417541
Arterial Occlusive Diseases Associate 16308497
Arthritis Psoriatic Stimulate 15482477