Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1395
Gene name Gene Name - the full gene name approved by the HGNC.
Corticotropin releasing hormone receptor 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CRHR2
Synonyms (NCBI Gene) Gene synonyms aliases
CRF-RB, CRF2, CRFR2, HM-CRF
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p14.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene belongs to the G-protein coupled receptor 2 family, and the subfamily of corticotropin releasing hormone receptor. This receptor shows high affinity for corticotropin releasing hormone (CRH), and also binds CRH-related pep
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs7793837 A>C,T Drug-response Genic upstream transcript variant, intron variant, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017454 hsa-miR-335-5p Microarray 18185580
MIRT909564 hsa-miR-1237 CLIP-seq
MIRT909565 hsa-miR-1248 CLIP-seq
MIRT909566 hsa-miR-1285 CLIP-seq
MIRT909567 hsa-miR-19a CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 11329063
GO:0005886 Component Plasma membrane IBA 21873635
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane TAS 8536644
GO:0007166 Process Cell surface receptor signaling pathway IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602034 2358 ENSG00000106113
Protein
UniProt ID Q13324
Protein name Corticotropin-releasing factor receptor 2 (CRF-R-2) (CRF-R2) (CRFR-2) (Corticotropin-releasing hormone receptor 2) (CRH-R-2) (CRH-R2)
Protein function G-protein coupled receptor for CRH (corticotropin-releasing factor), UCN (urocortin), UCN2 and UCN3. Has high affinity for UCN. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G protei
PDB 3N93 , 3N95 , 3N96 , 6PB1 , 7TRY , 7TS0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02793 HRM 37 101 Hormone receptor domain Family
PF00002 7tm_2 113 355 7 transmembrane receptor (Secretin family) Family
Sequence
Sequence length 411
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  cAMP signaling pathway
Neuroactive ligand-receptor interaction
Hormone signaling
Cushing syndrome
  Class B/2 (Secretin family receptors)
G alpha (s) signalling events
Synthesis, secretion, and deacylation of Ghrelin
ADORA2B mediated anti-inflammatory cytokines production
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Hypertension Hypertensive disease rs13306026 10742107
Unknown
Disease term Disease name Evidence References Source
Mental depression Mental Depression, Depressive disorder 15192151, 12832554, 18843268, 17467808 ClinVar
Diabetes Diabetes GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 36277017
Adrenocortical Adenoma Associate 37062723
Asthma Associate 18408560
Carcinoma Renal Cell Associate 19437022
Chronic Disease Associate 27773939
Colitis Associated Neoplasms Associate 31882463
Colitis Ulcerative Associate 23539366, 31882463
Colorectal Neoplasms Associate 28929494
COVID 19 Associate 34185889
Cushing Syndrome Associate 37062723, 37543650