Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 135
Gene Symbol: ADORA2A
ADORA2A 		0.300 Biomarker disease CTD_human Striatal adenosine-cannabinoid receptor interactions in rats over-expressing adenosine A2A receptors. 26526685 2016
Entrez Id: 10367
Gene Symbol: MICU1
MICU1 		0.300 Biomarker disease CTD_human Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling. 24336167 2014
Entrez Id: 6314
Gene Symbol: ATXN7
ATXN7 		0.300 Biomarker disease CTD_human Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report. 25664129 2014
Entrez Id: 3084
Gene Symbol: NRG1
NRG1 		0.300 Biomarker disease CTD_human Transmembrane domain Nrg1 mutant mice show altered susceptibility to the neurobehavioural actions of repeated THC exposure in adolescence. 22226049 2013
Entrez Id: 3064
Gene Symbol: HTT
HTT 		0.300 Biomarker disease CTD_human Loss of striatal type 1 cannabinoid receptors is a key pathogenic factor in Huntington's disease. 20929960 2011
Entrez Id: 1392
Gene Symbol: CRH
CRH 		0.300 Biomarker disease CTD_human Discovery of N-(1-ethylpropyl)-[3-methoxy-5-(2-methoxy-4-trifluoromethoxyphenyl)-6-methyl-pyrazin-2-yl]amine 59 (NGD 98-2): an orally active corticotropin releasing factor-1 (CRF-1) receptor antagonist. 21618986 2011
Entrez Id: 5173
Gene Symbol: PDYN
PDYN 		0.300 Biomarker disease CTD_human Methamphetamine-induced stereotypy correlates negatively with patch-enhanced prodynorphin and arc mRNA expression in the rat caudate putamen: the role of mu opioid receptor activation. 20298714 2010
Entrez Id: 4988
Gene Symbol: OPRM1
OPRM1 		0.300 Biomarker disease CTD_human Methamphetamine-induced stereotypy correlates negatively with patch-enhanced prodynorphin and arc mRNA expression in the rat caudate putamen: the role of mu opioid receptor activation. 20298714 2010
Entrez Id: 23237
Gene Symbol: ARC
ARC 		0.300 Biomarker disease CTD_human Methamphetamine-induced stereotypy correlates negatively with patch-enhanced prodynorphin and arc mRNA expression in the rat caudate putamen: the role of mu opioid receptor activation. 20298714 2010
Entrez Id: 43
Gene Symbol: ACHE
ACHE 		0.300 Biomarker disease CTD_human Acute effects of copper and mercury on the estuarine fish Pomatoschistus microps: linking biomarkers to behaviour. 19628251 2009
Entrez Id: 2348
Gene Symbol: FOLR1
FOLR1 		0.300 Biomarker disease CTD_human Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism. 19732866 2009
Entrez Id: 283989
Gene Symbol: TSEN54
TSEN54 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008
Entrez Id: 80746
Gene Symbol: TSEN2
TSEN2 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008
Entrez Id: 79042
Gene Symbol: TSEN34
TSEN34 		0.300 Biomarker disease CTD_human tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. 18711368 2008
Entrez Id: 10911
Gene Symbol: UTS2
UTS2 		0.300 Biomarker disease CTD_human Behavioral effects of urotensin-II centrally administered in mice. 16160878 2005
Entrez Id: 6558
Gene Symbol: SLC12A2
SLC12A2 		0.300 Biomarker disease CTD_human Presynaptic inhibition and spinal pain processing in mice: a possible role of the NKCC1 cation-chloride co-transporter in hyperalgesia. 15135928 2004
Entrez Id: 1814
Gene Symbol: DRD3
DRD3 		0.300 Therapeutic disease CTD_human Effects of oligonucleotide antisense to dopamine D3 receptor mRNA in a rodent model of behavioural sensitization to levodopa. 12535962 2003
Entrez Id: 6323
Gene Symbol: SCN1A
SCN1A 		0.300 Biomarker disease CTD_human Paroxysmal movement disorders in severe myoclonic epilepsy in infancy. 12907273 2003
Entrez Id: 7504
Gene Symbol: XK
XK 		0.300 Biomarker disease CTD_human McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings. 11261514 2001
Entrez Id: 1268
Gene Symbol: CNR1
CNR1 		0.300 Therapeutic disease CTD_human Cerebellar CB(1) receptor mediation of Delta(9)-THC-induced motor incoordination and its potentiation by ethanol and modulation by the cerebellar adenosinergic A(1) receptor in the mouse. 10802025 2000
Entrez Id: 2354
Gene Symbol: FOSB
FOSB 		0.300 Biomarker disease CTD_human Striatal fosB expression is causally linked with l-DOPA-induced abnormal involuntary movements and the associated upregulation of striatal prodynorphin mRNA in a rat model of Parkinson's disease. 10600402 1999
Entrez Id: 1813
Gene Symbol: DRD2
DRD2 		0.300 Biomarker disease CTD_human Abnormal involuntary movements: a study of dopaminergic receptor interaction. 6858777 1983
Entrez Id: 1812
Gene Symbol: DRD1
DRD1 		0.300 Biomarker disease CTD_human Abnormal involuntary movements: a study of dopaminergic receptor interaction. 6858777 1983