Gene Gene information from NCBI Gene database.
Entrez ID 2825
Gene name Chemerin chemokine-like receptor 2
Gene symbol CMKLR2
Synonyms (NCBI Gene)
GPR1
Chromosome 2
Chromosome location 2q33.3
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IBA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity TAS 7851889
GO:0005515 Function Protein binding IPI 24955142
GO:0005654 Component Nucleoplasm IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600239 4463 ENSG00000183671
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P46091
Protein name Chemerin-like receptor 2 (Chemerin chemokine-like receptor 2) (Chemokine-like receptor 2) (G-protein coupled receptor 1)
Protein function Receptor for chemoattractant adipokine chemerin/RARRES2 suggesting a role for this receptor in the regulation of inflammation and energy homesotasis (PubMed:18165312, PubMed:27716822). Signals mainly via beta-arrestin pathway. Binding of RARRES2
PDB 8JJP , 8XGM , 9L3Y
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 55 304 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in hippocampus.
Sequence
Sequence length 355
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
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
OBESITY GWAS catalog
★★☆☆☆
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
Alzheimer Disease Alzheimer disease Pubtator 25391383 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Squamous Cell Squamous cell carcinoma Pubtator 27907906 Associate
★☆☆☆☆
Found in Text Mining only
Choriocarcinoma Choriocarcinoma BEFREE 31241986
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus BEFREE 29948331
★☆☆☆☆
Found in Text Mining only
Hyperandrogenism Hyperandrogenism BEFREE 29793502
★☆☆☆☆
Found in Text Mining only
LEPTIN DEFICIENCY OR DYSFUNCTION LEPTIN DEFICIENCY OR DYSFUNCTION BEFREE 29414326
★☆☆☆☆
Found in Text Mining only
Mild cognitive disorder Cognitive disorder BEFREE 30178281
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31561459
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma Pubtator 39217334 Associate
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Ovarian neoplasm Pubtator 17371542, 20622109, 32279993 Associate
★☆☆☆☆
Found in Text Mining only