Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1814
Gene name Gene Name - the full gene name approved by the HGNC.
Dopamine receptor D3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DRD3
Synonyms (NCBI Gene) Gene synonyms aliases
D3DR, ETM1, FET1
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q13.31
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
miRTarBase ID miRNA Experiments Reference
MIRT029658 hsa-miR-26b-5p Microarray 19088304
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
126451 3024 ENSG00000151577
Protein
UniProt ID 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
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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
Asthma Asthma (childhood onset) N/A N/A GWAS
hereditary essential tremor Hereditary essential tremor N/A N/A ClinVar
Schizophrenia Schizophrenia, susceptibility to N/A N/A ClinVar
TREMOR tremor, hereditary essential, 1 N/A N/A ClinVar
Associations from Text Mining Disease 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