Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4987
Gene name Gene Name - the full gene name approved by the HGNC.
Opioid related nociceptin receptor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OPRL1
Synonyms (NCBI Gene) Gene synonyms aliases
KOR-3, KOR3, NOCIR, NOP, NOPr, OOR, OPRL, ORL1, PNOCR
Chromosome Chromosome number
20
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
20q13.33
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the 7 transmembrane-spanning G protein-coupled receptor family, and functions as a receptor for the endogenous, opioid-related neuropeptide, nociceptin/orphanin FQ. This receptor-ligand system modulates a va
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT529744 hsa-miR-6733-3p PAR-CLIP 22012620
MIRT529742 hsa-miR-6729-3p PAR-CLIP 22012620
MIRT529741 hsa-miR-6793-3p PAR-CLIP 22012620
MIRT529740 hsa-miR-6801-3p PAR-CLIP 22012620
MIRT529739 hsa-miR-6810-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001626 Function Nociceptin receptor activity IBA 21873635
GO:0001626 Function Nociceptin receptor activity IDA 10571060, 12568343
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0004930 Function G protein-coupled receptor activity IMP 8137918
GO:0004930 Function G protein-coupled receptor activity IPI 10571060
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602548 8155 ENSG00000125510
Protein
UniProt ID P41146
Protein name Nociceptin receptor (Kappa-type 3 opioid receptor) (KOR-3) (Orphanin FQ receptor)
Protein function G-protein coupled opioid receptor that functions as a receptor for the endogenous neuropeptide nociceptin. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the
PDB 4EA3 , 5DHG , 5DHH , 8F7X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 68 319 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in blood leukocytes. {ECO:0000269|PubMed:7500847}.
Sequence
Sequence length 370
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Neuroactive ligand-receptor interaction
Hormone signaling
  Peptide ligand-binding receptors
G alpha (i) signalling events
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Metabolic Syndrome Metabolic Syndrome GWAS
Diabetes Diabetes GWAS
Duodenal Ulcer Duodenal Ulcer GWAS
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 30152845
Arthritis Infectious Associate 21324928
Bronchopulmonary Dysplasia Stimulate 35509863
Cholangitis Sclerosing Associate 38302916
Colitis Ulcerative Associate 38302916
Inflammation Associate 21547539, 39652903
Inflammatory Bowel Diseases Associate 39652903
Metabolic Syndrome Associate 35168826
Neoplasms Associate 21324928, 36011316
Pain Associate 30466988, 39652903