DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Parkinsonian-like locomotor impairment in mice lacking dopamine D2 receptors. 7566118 1995
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Therapeutic disease CTD_human ABT-431: the diacetyl prodrug of A-86929, a potent and selective dopamine D1 receptor agonist: in vitro characterization and effects in animal models of Parkinson's disease. 8558425 1996
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Absence of opiate rewarding effects in mice lacking dopamine D2 receptors. 9252189 1997
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Antiproliferative role of dopamine: loss of D2 receptors causes hormonal dysfunction and pituitary hyperplasia. 9247268 1997
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Absence of dopaminergic control on melanotrophs leads to Cushing's-like syndrome in mice. 9717839 1998
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Thus our results do not support a role for the DRD2 locus to develop PD. 10515181 1999
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Further, DRD2 variants have been implicated in Parkinson's disease (PD) and in iatrogenically-induced movement disorders, as well as in certain migraineurs. 11256581 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Genetic variation in the DRD2 gene may influence the risk of developing PD, thus confirming that the DRD2 gene is a susceptibility locus for PD. 10634251 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In this study, we investigated the hypothesis that a TaqI repeat fragment length polymorphism in the dopamine D2 receptor gene may be associated with PD. 11104188 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Neuroprotective role of dopamine against hippocampal cell death. 11069974 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE This polymorphism may be in linkage disequilibrium with a mutation in DRD2 or a nearby gene that predisposes to drug-induced hallucinations which occur later in the course of idiopathic Parkinson's disease. 10739171 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE When genotypes for DRD2 were considered in combination with genotypes for intron 13 of MAO-B, genotype combinations with high risk of Parkinson's disease were found; although the MAO-B/DRD2 interaction did not reach statistical significance after Bonferroni correction for multiple comparisons, these results are suggestive of a possible synergism between MAOB and DRD2 genes with respect to Parkinson's disease. 10990520 2000
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE The -141C Ins/Del polymorphism of the dopamine D2 receptor gene is not associated with either migraine or Parkinson's disease. 11409701 2001
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE We tested for gender-specific interactions between smoking and genetic polymorphisms of monoamine oxidase B (MAO-B) intron 13 (G or A allele), monoamine oxidase A (MAO-A) EcoRV (Yor N allele), and dopamine D2 recepor (DRD2) Taq1B (B1 or B2 allele) in a case-control study of 186 incident idiopathic Parkinson's disease (PD) cases and 296 age- and gender-matched controls. 12428723 2002
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease MGD Activity, non-selective attention and emotionality in dopamine D2/D3 receptor knock-out mice. 11864730 2002
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Dopamine D2 receptor TaqIA and TaqIB polymorphisms in Parkinson's disease. 12722176 2003
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 AlteredExpression disease BEFREE No alteration in the level of dopamine D2 receptor or dopamine transporter mRNA was found in either lobule in patients with Parkinson's disease. 14622169 2003
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Our results show a significant association between the dopamine D2 receptor gene polymorphism Taq IA and SOS in PD. 15390060 2004
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Previously, we found a significant association between the dopamine D2 receptor gene polymorphism Taq IA and sudden onset of sleep in patients with Parkinson disease. 16124668 2005
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease BEFREE Thus, alterations in RGS9-2 may be a key factor in the pathway leading from D2DRs to the side effects associated with the treatment both of psychoses and Parkinson's disease. 15728856 2005
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Patients Two hundred fifty patients with Parkinson disease were screened for the presence or absence of PDD following a short-term levodopa administration, and 215 subjects were available for further evaluations, including genotypic analysis of the CA dinucleotide short tandem repeat (CAn-STR) polymorphism located in the dopamine receptor D2 gene (DRD2). 15824260 2005
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE In the present study, we investigated this effect in Parkinson's disease (PD) patients carrying the DRD2 TaqIA A1 allelic variant. 17147698 2007
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE Genotype combinations characterized by the presence of two variant genotypes on their corresponding loci revealed that four combinations of GSTT1 null and MnSOD(-9Val) or GST null and MAOB-G or CYP2E1*5B and MAO-B-AG or CYP2E1*5B and DRD2 (Taq1A-het) genotypes in the patients exhibited severalfold higher and significant association with risk to PD. 18327668 2008
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 GeneticVariation disease BEFREE We conclude that the DRD2 TaqIA polymorphism alone has no pivotal role for interindividual variability of dopaminergic requirement in PD. 18175338 2008
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker disease RGD Melatonin reduces the neuronal loss, downregulation of dopamine transporter, and upregulation of D2 receptor in rotenone-induced parkinsonian rats. 18289173 2008