Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 Biomarker MGD

Entrez Id: 7019
Gene Symbol: TFAM
TFAM
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD

Entrez Id: 56652
Gene Symbol: TWNK
TWNK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.240 Biomarker MGD

Entrez Id: 10533
Gene Symbol: ATG7
ATG7
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.230 Biomarker MGD

Entrez Id: 54700
Gene Symbol: RRN3
RRN3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker MGD

Entrez Id: 1352
Gene Symbol: COX10
COX10
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker MGD

Entrez Id: 7054
Gene Symbol: TH
TH
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker RGD Grafting fibroblasts genetically modified to produce L-dopa in a rat model of Parkinson disease. 2573072

1989

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Parkinsonian-like locomotor impairment in mice lacking dopamine D2 receptors. 7566118

1995

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Absence of opiate rewarding effects in mice lacking dopamine D2 receptors. 9252189

1997

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Antiproliferative role of dopamine: loss of D2 receptors causes hormonal dysfunction and pituitary hyperplasia. 9247268

1997

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Absence of dopaminergic control on melanotrophs leads to Cushing's-like syndrome in mice. 9717839

1998

Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD Our results demonstrate a selective and specific deficit of DA and absence of DAergic neurons in the mesencephalic structures of Nurr1-deficient mice, which resembles the pattern similar to that seen in patients with Parkinson's disease (PD). 10506516

1999

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Neuroprotective role of dopamine against hippocampal cell death. 11069974

2000

Entrez Id: 5179
Gene Symbol: PENK
PENK
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.230 Biomarker RGD Relevance between striatal expression of Fos, proenkephalin mRNA, prodynorphin mRNA and rotation induced by l-stepholidine in 6-hydroxydopamine-lesioned rats. 11501038

2000

Entrez Id: 6622
Gene Symbol: SNCA
SNCA
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.700 Biomarker RGD Two missense mutations of the alpha-synuclein (alpha-syn; A30P and A53T) have been described in several families with an autosomal dominant form of PD. alpha-Syn also constitutes one of the main components of Lewy bodies in sporadic cases of PD. 12122208

2002

Entrez Id: 1813
Gene Symbol: DRD2
DRD2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker MGD Activity, non-selective attention and emotionality in dopamine D2/D3 receptor knock-out mice. 11864730

2002

Entrez Id: 1644
Gene Symbol: DDC
DDC
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker RGD Effects of benserazide on L-DOPA-derived extracellular dopamine levels and aromatic L-amino acid decarboxylase activity in the striatum of 6-hydroxydopamine-lesioned rats. 12703659

2003

Entrez Id: 5309
Gene Symbol: PITX3
PITX3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD Selective loss of dopaminergic neurons in the substantia nigra of Pitx3-deficient aphakia mice. 12829322

2003

Entrez Id: 111
Gene Symbol: ADCY5
ADCY5
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker MGD Motor dysfunction in type 5 adenylyl cyclase-null mice. 12665504

2003

Entrez Id: 1644
Gene Symbol: DDC
DDC
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker RGD Degeneration of dopaminergic neurons triggers an expression of individual enzymes of dopamine synthesis in non-dopaminergic neurons of the arcuate nucleus in adult rats. 15935614

2005

Entrez Id: 4929
Gene Symbol: NR4A2
NR4A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD Our data indicate that Nurr1 plays an important role in the functional maintenance and survival of nigral DAergic neurons and suggest that the Nurr1+/- mouse is a useful animal model to study the pathogenesis of Parkinson disease (PD) and to explore disease-modifying strategies. 15589522

2005

Entrez Id: 5309
Gene Symbol: PITX3
PITX3
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.300 Biomarker MGD 3,4-dihydroxyphenylalanine reverses the motor deficits in Pitx3-deficient aphakia mice: behavioral characterization of a novel genetic model of Parkinson's disease. 15728853

2005

Entrez Id: 1742
Gene Symbol: DLG4
DLG4
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.220 Biomarker RGD Here, we show that expression and subcellular distribution of PSD-95 and SAP97 are altered in the striatum of unilateral 6-OHDA-lesioned rats following repeated vehicle (a model of PD) or L-DOPA administration (a model of L-DOPA-induced dyskinesia). 15703272

2005

Entrez Id: 1739
Gene Symbol: DLG1
DLG1
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.200 Biomarker RGD Here, we show that expression and subcellular distribution of PSD-95 and SAP97 are altered in the striatum of unilateral 6-OHDA-lesioned rats following repeated vehicle (a model of PD) or L-DOPA administration (a model of L-DOPA-induced dyskinesia). 15703272

2005

Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
0.600 Biomarker RGD Vesicular monoamine transporter-2 and aromatic L-amino acid decarboxylase gene therapy prevents development of motor complications in parkinsonian rats after chronic intermittent L-3,4-dihydroxyphenylalanine administration. 16269145

2006