Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1816
Gene name Gene Name - the full gene name approved by the HGNC.
Dopamine receptor D5
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DRD5
Synonyms (NCBI Gene) Gene synonyms aliases
DBDR, DRD1B, DRD1L2
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p16.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes the D5 subtype of the dopamine receptor. The D5 subtype is a G-protein coupled receptor which stimulates adenylyl cyclase. This receptor is expressed in neurons in the limbic regions of the brain. It has a 10-fold higher affinity for dop
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017477 hsa-miR-335-5p Microarray 18185580
MIRT945370 hsa-miR-1253 CLIP-seq
MIRT945371 hsa-miR-3184 CLIP-seq
MIRT945372 hsa-miR-423-5p CLIP-seq
MIRT945373 hsa-miR-4477b CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs IBA 21873635
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs TAS 9457173
GO:0001963 Process Synaptic transmission, dopaminergic NAS 11036203
GO:0001975 Process Response to amphetamine IEA
GO:0001992 Process Regulation of systemic arterial blood pressure by vasopressin IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
126453 3026 ENSG00000169676
Protein
UniProt ID P21918
Protein name D(1B) dopamine receptor (D(5) dopamine receptor) (D1beta dopamine receptor) (Dopamine D5 receptor)
Protein function Dopamine receptor whose activity is mediated by G proteins which activate adenylyl cyclase.
PDB 8IRV
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 57 359 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Neuron-specific, localized primarily within limbic regions of the brain. {ECO:0000269|PubMed:1834671}.
Sequence
Sequence length 477
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
cAMP signaling pathway
Neuroactive ligand-receptor interaction
Hormone signaling
Dopaminergic synapse
  Dopamine receptors
G alpha (s) signalling events
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
Attention deficit hyperactivity disorder Attention Deficit Disorder, Attention deficit hyperactivity disorder rs786205019 14699430, 14732906
Unknown
Disease term Disease name Evidence References Source
Mental depression Endogenous depression, Depressive disorder, Unipolar Depression, Depressive Syndrome, Depression, Neurotic 14708030 ClinVar
Language Delay And Attention Deficit-Hyperactivity Disorder/Cognitive Impairment With Or Without Cardiac Arrhythmia attention deficit-hyperactivity disorder GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 29670116
Attention Deficit Disorder with Hyperactivity Associate 11923911, 14732906, 16380908, 22562805
Breast Neoplasms Associate 25556472
Disruptive Impulse Control and Conduct Disorders Associate 25896831
Glioblastoma Associate 30559168, 36477472
Glioma Associate 28339748
HIV Infections Associate 37376663
Inflammation Inhibit 26808524
Leukemia Associate 24517546
Mental Disorders Associate 24668635