Gene Gene information from NCBI Gene database.
Entrez ID 3579
Gene name C-X-C motif chemokine receptor 2
Gene symbol CXCR2
Synonyms (NCBI Gene)
CD182CDw128bCMKAR2IL8R2IL8RAIL8RBWHIMS2
Chromosome 2
Chromosome location 2q35
Summary 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.
1
SNP ID Visualize variation Clinical significance Consequence
rs1574542732 A>T Likely-pathogenic Coding sequence variant, stop gained
miRNA miRNA information provided by mirtarbase database.
134
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 factors information provided by TRRUST V2 database.
6
Transcription factor Regulation Reference
CEBPA Unknown 18555777
NFKB1 Activation 19156404
NFKB1 Unknown 18555777
RELA Activation 19156404
RELA Unknown 18555777
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
48
GO ID Ontology Definition Evidence Reference
GO:0002407 Process Dendritic cell chemotaxis IEA
GO:0002407 Process Dendritic cell chemotaxis TAS 16621978
GO:0004918 Function Interleukin-8 receptor activity IDA 10820279
GO:0004918 Function Interleukin-8 receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity IDA 10438939
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
146928 6027 ENSG00000180871
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
25
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
WHIM syndrome 2 Pathogenic; Likely pathogenic rs2106109435, rs1273183086 RCV001532874
RCV001824265
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ANKYLOSING SPONDYLITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ARTHRITIS, JUVENILE CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOSOMAL RECESSIVE SEVERE CONGENITAL NEUTROPENIA DUE TO C-X-C MOTIF CHEMOKINE RECEPTOR 2 DEFICIENCY Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTOSOMAL RECESSIVE SEVERE CONGENITAL NEUTROPENIA DUE TO CXCR2 DEFICIENCY GenCC, Orphanet
GenCC, Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Acute monocytic leukemia Monocytic Leukemia BEFREE 25810490
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma Adenocarcinoma BEFREE 22389383
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of lung (disorder) Lung adenocarcinoma BEFREE 21328342, 23204236
★☆☆☆☆
Found in Text Mining only
Adenocarcinoma of prostate Prostate adenocarcinoma BEFREE 31801883
★☆☆☆☆
Found in Text Mining only
Allergic rhinitis (disorder) Allergic rhinitis BEFREE 12532104
★☆☆☆☆
Found in Text Mining only
Allergic sensitization Allergic Sensitization BEFREE 26086549
★☆☆☆☆
Found in Text Mining only
Alveolitis, Fibrosing Alveolitis BEFREE 10902769
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Alzheimer disease Pubtator 33804025 Associate
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis BEFREE 21084199
★☆☆☆☆
Found in Text Mining only
Anemia, Sickle Cell Anemia BEFREE 21383500
★☆☆☆☆
Found in Text Mining only