Gene Gene information from NCBI Gene database.
Entrez ID 1812
Gene name Dopamine receptor D1
Gene symbol DRD1
Synonyms (NCBI Gene)
D1RDADRDRD1A
Chromosome 5
Chromosome location 5q35.2
Summary This gene encodes the D1 subtype of the dopamine receptor. The D1 subtype is the most abundant dopamine receptor in the central nervous system. This G-protein coupled receptor stimulates adenylyl cyclase and activates cyclic AMP-dependent protein kinases.
miRNA miRNA information provided by mirtarbase database.
44
miRTarBase ID miRNA Experiments Reference
MIRT000044 hsa-miR-504-5p Luciferase reporter assay 19135651
MIRT000044 hsa-miR-504-5p Luciferase reporter assay 19135651
MIRT438103 hsa-miR-382-5p Luciferase reporter assay 23873704
MIRT438103 hsa-miR-382-5p Luciferase reporter assay 23873704
MIRT736201 hsa-miR-15a-5p Luciferase reporter assayWestern blottingqRT-PCR 31858826
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
TFAP2B Unknown 10640692
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
114
GO ID Ontology Definition Evidence Reference
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs IBA
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs IDA 2144334, 2168520
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs IEA
GO:0001588 Function Dopamine neurotransmitter receptor activity, coupled via Gs IMP 1282671, 7838121
GO:0001659 Process Temperature homeostasis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
126449 3020 ENSG00000184845
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P21728
Protein name D(1A) dopamine receptor (Dopamine D1 receptor)
Protein function Dopamine receptor whose activity is mediated by G proteins which activate adenylyl cyclase.
PDB 7CKW , 7CKX , 7CKY , 7CKZ , 7CRH , 7F0T , 7F1O , 7F1Z , 7F23 , 7F24 , 7JOZ , 7JV5 , 7JVP , 7JVQ , 7LJC , 7LJD , 7X2C , 7X2D , 7X2F , 8IRR , 8JXR , 8JXS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 40 331 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in caudate, nucleus accumbens and in the olfactory tubercle. {ECO:0000269|PubMed:2144334}.
Sequence
Sequence length 446
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
Gap junction
Dopaminergic synapse
Parkinson disease
Cocaine addiction
Amphetamine addiction
Morphine addiction
Alcoholism
  Dopamine receptors
G alpha (s) signalling events
ADORA2B mediated anti-inflammatory cytokines production
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
24
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AMPHETAMINE OR RELATED ACTING SYMPATHOMIMETIC ABUSE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AMPHETAMINE-RELATED DISORDERS CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISTIC DISORDER CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adrenal Cortex Diseases Adrenal Cortex Diseases BEFREE 24618367
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease, Late Onset Alzheimer disease BEFREE 11723200
★☆☆☆☆
Found in Text Mining only
Amyloidosis Amyloidosis BEFREE 29321592, 31413143
★☆☆☆☆
Found in Text Mining only
Anxiety Anxiety Disorder BEFREE 30500462
★☆☆☆☆
Found in Text Mining only
Anxiety Disorders Anxiety Disorder BEFREE 30500462
★☆☆☆☆
Found in Text Mining only
Astrocytoma Astrocytoma BEFREE 31478179
★☆☆☆☆
Found in Text Mining only
Attention Deficit Disorder with Hyperactivity Attention deficit hyperactivity disorder Pubtator 24410775, 28237458 Associate
★☆☆☆☆
Found in Text Mining only
Attention deficit hyperactivity disorder Attention Deficit Hyperactivity Disorder BEFREE 12377397, 14569274, 15717291, 17310237, 17679637, 22404661, 24410775, 28237458, 9603612
★☆☆☆☆
Found in Text Mining only
Attention deficit hyperactivity disorder Attention Deficit Hyperactivity Disorder LHGDN 15717291
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorders Autism Spectrum Disorder BEFREE 18205172
★☆☆☆☆
Found in Text Mining only