Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 85301
Gene Symbol: COL27A1
COL27A1
0.110 GeneticVariation disease GWASDB Genome-wide association study of Tourette's syndrome. 22889924 2013
Entrez Id: 1106
Gene Symbol: CHD2
CHD2
0.300 Biomarker disease GENOMICS_ENGLAND CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. 25294932 2014
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.300 Therapeutic disease RGD Results demonstrated that Ning-dong granule effectively inhibited stereotype actions and Tourette's syndrome symptoms by promoting dopamine metabolism, reducing dopamine levels in the striatum, increasing homovanillic acid content in sera, and reducing mRNA expression of DRD2 in the striatum. 22876458 2012
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.300 Biomarker disease RGD NDG could increase the HVA content in sera (P<0.05), meanwhile downregulate the expression of DRD2 mRNA in striatum (P<0.05), and inhibit the stereotyped behaviors induced by Apo (P<0.01) in TS rats, the same effects with Hal. 19467315 2009
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 Biomarker disease MGD Elevated anxiety due to Slitrk1 dysfunction may contribute to the pathogenesis of neuropsychiatric diseases such as Tourette's syndrome and trichotillomania. 18794888 2010
Entrez Id: 3067
Gene Symbol: HDC
HDC
0.680 Biomarker disease MGD These data confirm histidine decarboxylase deficiency as a rare cause of TS and identify HA-DA interactions in the basal ganglia as an important locus of pathology. 24411733 2014
Entrez Id: 3067
Gene Symbol: HDC
HDC
0.680 Biomarker disease MGD Intrathecally-administered histamine facilitates nociception through tachykinin NK1 and histamine H1 receptors: a study in histidine decarboxylase gene knockout mice. 16212954 2005
Entrez Id: 3067
Gene Symbol: HDC
HDC
0.680 Biomarker disease MGD Mice lacking histidine decarboxylase exhibit abnormal mast cells. 11478947 2001
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.290 Biomarker disease MGD Hyperactivity and impaired response habituation in hyperdopaminergic mice. 11172062 2001
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.290 Biomarker disease MGD Sequential super-stereotypy of an instinctive fixed action pattern in hyper-dopaminergic mutant mice: a model of obsessive compulsive disorder and Tourette's. 15710042 2005
Entrez Id: 4233
Gene Symbol: MET
MET
0.200 Biomarker disease MGD
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 GeneticVariation disease LHGDN The negative results of the SLITRK1 analysis point to genetic heterogeneity in TS. 17712845 2007
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 Biomarker disease LHGDN SLITRK1 trouble in Tourette's syndrome. 16323357 2005
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 Biomarker disease LHGDN Psychopathological features of obsessive-compulsive disorder in an Italian family with Gilles de la Tourette syndrome not linked to the SLITRK1 gene. 18722020 2008
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 GeneticVariation disease LHGDN Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. 18413575 2008
Entrez Id: 114798
Gene Symbol: SLITRK1
SLITRK1
0.700 GeneticVariation disease LHGDN Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome. 18004766 2008
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.300 Biomarker disease LHGDN This study has demonstrated an association between the dopamine receptor D2 gene and Tourette syndrome. 16194726 2005
Entrez Id: 1813
Gene Symbol: DRD2
DRD2
0.300 Biomarker disease LHGDN Increased prefrontal D2 protein in Tourette syndrome: a postmortem analysis of frontal cortex and striatum. 15050438 2004
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.290 GeneticVariation disease LHGDN In summary, allele frequencies did not differ between cases and controls, but DAT1 genotype accounted for variations of tic severity within the TS group. 17508355 2007
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.290 GeneticVariation disease LHGDN A statistical re-evaluation of the DAT1 DdeI polymorphism following population stratification confirmed the association for the TS-total and TS-only groups, but the degree of significance was reduced (P = 0.017 and P = 0.016, respectively). 17171650 2007
Entrez Id: 26047
Gene Symbol: CNTNAP2
CNTNAP2
0.030 Biomarker disease LHGDN We hypothesize that disruption or decreased expression of CNTNAP2 could lead to a disturbed distribution of the K(+) channels in the nervous system, thereby influencing conduction and/or repolarization of action potentials, causing unwanted actions or movements in GTS. 12809671 2003
Entrez Id: 8910
Gene Symbol: SGCE
SGCE
0.020 GeneticVariation disease LHGDN Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene. 17702041 2007
Entrez Id: 3359
Gene Symbol: HTR3A
HTR3A
0.020 GeneticVariation disease LHGDN In our study both serotonin receptor subunit genes, HTR3A and HTR3B, were examined for sequence variations in GTS patients. 16314763 2005
Entrez Id: 9177
Gene Symbol: HTR3B
HTR3B
0.010 GeneticVariation disease LHGDN In our study both serotonin receptor subunit genes, HTR3A and HTR3B, were examined for sequence variations in GTS patients. 16314763 2005
Entrez Id: 121278
Gene Symbol: TPH2
TPH2
0.010 GeneticVariation disease LHGDN Role of the novel tryptophan hydroxylase-2 gene in Tourette syndrome. 17592484 2007