Gene Gene information from NCBI Gene database.
Entrez ID 1814
Gene name Dopamine receptor D3
Gene symbol DRD3
Synonyms (NCBI Gene)
D3DRETM1FET1
Chromosome 3
Chromosome location 3q13.31
Summary This gene encodes the D3 subtype of the five (D1-D5) dopamine receptors. The activity of the D3 subtype receptor is mediated by G proteins which inhibit adenylyl cyclase. This receptor is localized to the limbic areas of the brain, which are associated wi
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs6280 C>T Risk-factor, benign, likely-benign Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
1
miRTarBase ID miRNA Experiments Reference
MIRT029658 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
62
GO ID Ontology Definition Evidence Reference
GO:0001591 Function Dopamine neurotransmitter receptor activity, coupled via Gi/Go IBA
GO:0001591 Function Dopamine neurotransmitter receptor activity, coupled via Gi/Go IDA 8301582
GO:0001591 Function Dopamine neurotransmitter receptor activity, coupled via Gi/Go IEA
GO:0001591 Function Dopamine neurotransmitter receptor activity, coupled via Gi/Go ISS
GO:0001963 Process Synaptic transmission, dopaminergic IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
126451 3024 ENSG00000151577
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P35462
Protein name D(3) dopamine receptor (Dopamine D3 receptor)
Protein function Dopamine receptor whose activity is mediated by G proteins which inhibit adenylyl cyclase. Promotes cell proliferation.
PDB 3PBL , 7CMU , 7CMV , 8IRT , 9F33 , 9F34
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 46 383 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Brain.
Sequence
Sequence length 400
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Neuroactive ligand-receptor interaction
Hormone signaling
Dopaminergic synapse
  Dopamine receptors
G alpha (i) signalling events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
37
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
DRD3-related disorder Uncertain significance; Conflicting classifications of pathogenicity; Likely benign; Benign rs2107825397, rs201882973, rs150042478, rs3732783, rs6280, rs77498054 RCV003400123
RCV005356435
RCV003972443
RCV003972444
RCV003974838
RCV003981357
Essential tremor, susceptibility to Benign; Likely benign rs6280 RCV000018258
Hereditary essential tremor Uncertain significance rs886057789, rs200825904, rs199852439, rs75091114, rs886057790, rs201561838, rs886057788, rs200206712, rs201872343, rs886057791 RCV000366836
RCV000297108
RCV000397000
RCV000272180
RCV000379475
RCV000336537
RCV000301133
RCV000330956
RCV000288465
RCV000315005
Schizophrenia, susceptibility to Benign; Likely benign rs6280 RCV000018257
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Acute Pain Associate 25102390
Adenocarcinoma of Lung Associate 30419062
Akathisia Drug Induced Associate 23226551
Alzheimer Disease Associate 11723200
Anemia Sickle Cell Associate 25102390, 35285297
Antisocial Personality Disorder Associate 23891037
Autism Spectrum Disorder Associate 21691864, 23032108
Autistic Disorder Associate 25158632, 28470827, 29249220
Bipolar Disorder Associate 27310943, 28751646
Carcinoma Hepatocellular Associate 36456906