Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4985
Gene name Gene Name - the full gene name approved by the HGNC.
Opioid receptor delta 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
OPRD1
Synonyms (NCBI Gene) Gene synonyms aliases
DOP, DOR, DOR1, OPRD
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p35.3
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs678849 C>G,T Drug-response Intron variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT037618 hsa-miR-744-5p CLASH 23622248
MIRT574284 hsa-miR-1295b-5p PAR-CLIP 20371350
MIRT574283 hsa-miR-1912 PAR-CLIP 20371350
MIRT574282 hsa-miR-500b-3p PAR-CLIP 20371350
MIRT574281 hsa-miR-5090 PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004985 Function G protein-coupled opioid receptor activity IDA 22184124
GO:0004985 Function G protein-coupled opioid receptor activity IEA
GO:0005515 Function Protein binding IPI 15086532, 20528919, 32296183
GO:0005886 Component Plasma membrane IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
165195 8153 ENSG00000116329
Protein
UniProt ID P41143
Protein name Delta-type opioid receptor (D-OR-1) (DOR-1)
Protein function G-protein coupled receptor that functions as a receptor for endogenous enkephalins and for a subset of other opioids. Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and mo
PDB 4N6H , 4RWA , 4RWD , 6PT2 , 6PT3 , 8F7S , 8Y45
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 66 318 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in oocytes (at protein level). Detected in brain cortex, hypothalamus, hippocampus and olfactory bulb. Detected in oocytes. {ECO:0000269|PubMed:22417668, ECO:0000269|PubMed:7808419}.
Sequence
Sequence length 372
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  cGMP-PKG signaling pathway
Sphingolipid signaling pathway
Neuroactive ligand-receptor interaction
Hormone signaling
  Peptide ligand-binding receptors
G alpha (i) signalling events
Interleukin-4 and Interleukin-13 signaling
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 28253273, 30152845, 33522999
Brain Diseases Associate 23427138
Cystic Fibrosis Associate 27572404
Cystic Fibrosis Inhibit 35467369
Gout Associate 35908776
Hepatitis Autoimmune Associate 18753988
Hepatitis B Chronic Associate 18753988
Hepatitis C Chronic Associate 18753988
Mental Disorders Associate 34407719
Neurodegenerative Diseases Associate 23427138