Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23435
Gene Symbol: TARDBP
TARDBP
0.010 GeneticVariation phenotype BEFREE TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. 19609911 2009
Entrez Id: 6872
Gene Symbol: TAF1
TAF1
0.100 Biomarker phenotype HPO
Entrez Id: 6834
Gene Symbol: SURF1
SURF1
0.100 Biomarker phenotype HPO
Entrez Id: 6487
Gene Symbol: ST3GAL3
ST3GAL3
0.100 Biomarker phenotype HPO
Entrez Id: 6750
Gene Symbol: SST
SST
0.010 Biomarker phenotype BEFREE Evidence is discussed which may support a role of somatostatin deficiency in the pathophysiology of chorea. 6167683 1981
Entrez Id: 23583
Gene Symbol: SMUG1
SMUG1
0.010 Biomarker phenotype BEFREE Glucose Hypermetabolism in Contralateral Basal Ganglia Demonstrated by Serial FDG PET/CT Scans in a Patient With SLE Chorea. 27819860 2017
Entrez Id: 10479
Gene Symbol: SLC9A6
SLC9A6
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6535
Gene Symbol: SLC6A8
SLC6A8
0.100 Biomarker phenotype HPO
Entrez Id: 6531
Gene Symbol: SLC6A3
SLC6A3
0.100 Biomarker phenotype HPO
Entrez Id: 50651
Gene Symbol: SLC45A1
SLC45A1
0.100 Biomarker phenotype HPO
Entrez Id: 6513
Gene Symbol: SLC2A1
SLC2A1
0.010 GeneticVariation phenotype BEFREE Childhood chorea with cerebral hypotrophy: a treatable GLUT1 energy failure syndrome. 19901175 2009
Entrez Id: 6575
Gene Symbol: SLC20A2
SLC20A2
0.100 Biomarker phenotype HPO
Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
0.040 Biomarker phenotype BEFREE Expert commentary: Inhibitors of presynaptic vesicular monoamine transporter type 2 (VMAT2) that cause striatal dopamine depletion, such as tetrabenazine, deutetrabenazine, and valbenazine, are considered the treatment of choice in patients with chorea. 29120264 2018
Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
0.040 Biomarker phenotype BEFREE Oral deutetrabenazine (Austedo™), a reversible inhibitor of vesicular monoamine transporter type 2 (VMAT2) that is structurally related to tetrabenazine is approved for the treatment of chorea symptoms associated with Huntington's disease (HD). 29080203 2017
Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
0.040 Biomarker phenotype BEFREE Areas covered: Deutetrabenazine is the first deuterated drug and second drug after tetrabenazine, the classic vesicular monoamine transporter type 2 (VMAT2) inhibitor, to receive approval for the treatment of chorea associated with HD. 29996061 2018
Entrez Id: 6571
Gene Symbol: SLC18A2
SLC18A2
0.040 Biomarker phenotype BEFREE The recent development of selective vesicular monoamine transporter blocking agents has allowed for targeted chorea management with minimal side effects. 30255459 2018
Entrez Id: 6567
Gene Symbol: SLC16A2
SLC16A2
0.010 Biomarker phenotype LHGDN X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene. 15834651 2005
Entrez Id: 8910
Gene Symbol: SGCE
SGCE
0.010 GeneticVariation phenotype BEFREE The mutually exclusive appearance of lightning-like myoclonic jerks triggered by action in SGCE mutation carriers and of continuous chorea of all limbs in TITF-1 mutation carriers phenotypically discriminated both genetic disorders. 17702043 2007
Entrez Id: 51091
Gene Symbol: SEPSECS
SEPSECS
0.100 Biomarker phenotype HPO
Entrez Id: 9997
Gene Symbol: SCO2
SCO2
0.100 Biomarker phenotype HPO
Entrez Id: 6301
Gene Symbol: SARS1
SARS1
0.100 Biomarker phenotype HPO
Entrez Id: 51319
Gene Symbol: RSRC1
RSRC1
0.100 Biomarker phenotype HPO
Entrez Id: 54476
Gene Symbol: RNF216
RNF216
0.010 Biomarker phenotype BEFREE Our study thus challenges the oligogenic inheritance model and emphasizes chorea as an essential clinical feature in RNF216-mediated neurodegeneration. 25841028 2015
Entrez Id: 23221
Gene Symbol: RHOBTB2
RHOBTB2
0.100 CausalMutation phenotype CLINVAR
Entrez Id: 23221
Gene Symbol: RHOBTB2
RHOBTB2
0.100 Biomarker phenotype HPO