tourette syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A tic disorder that is characterized by multiple physical (motor) tics and at least one vocal (phonic) tic present for more than a year. (Human Disease Ontology, DOID_11119)
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Genes

22 genes associated with the disease tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACP1 acid phosphatase 1, soluble
ADRA2A adrenoceptor alpha 2A
COMT catechol-O-methyltransferase
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
DRD4 dopamine receptor D4
FGF10 fibroblast growth factor 10
GDNF glial cell derived neurotrophic factor
HCN1 hyperpolarization activated cyclic nucleotide gated potassium channel 1
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
ISL1 ISL LIM homeobox 1
ITGA1 integrin, alpha 1
MAOA monoamine oxidase A
ROBO3 roundabout, axon guidance receptor, homolog 3 (Drosophila)
ROBO4 roundabout, axon guidance receptor, homolog 4 (Drosophila)
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
SLITRK1 SLIT and NTRK-like family, member 1
TDO2 tryptophan 2,3-dioxygenase