Tic Disorder Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A specific developmental disorder that is characterized by the persistent presence of involuntary brief movements or sounds occuring intermittently and unpredictably out of a background of normal motor activity. (Human Disease Ontology, DOID_2769)
External Link https://www.disgenet.org/browser/0/1/0/C0040188
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Genes

33 genes associated with the disease Tic Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
ADRA2A adrenoceptor alpha 2A
ALDH1A1 aldehyde dehydrogenase 1 family, member A1
ATP7B ATPase, Cu++ transporting, beta polypeptide
BECN1 beclin 1, autophagy related
BLM Bloom syndrome, RecQ helicase-like
BRCA1 breast cancer 1, early onset
CD24 CD24 molecule
CD44 CD44 molecule (Indian blood group)
DRD4 dopamine receptor D4
ECT2 epithelial cell transforming 2
ENO2 enolase 2 (gamma, neuronal)
EZH2 enhancer of zeste 2 polycomb repressive complex 2 subunit
F10 coagulation factor X
GNA13 guanine nucleotide binding protein (G protein), alpha 13
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
HRH3 histamine receptor H3
HSPD1 heat shock 60kDa protein 1 (chaperonin)
INS insulin
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
MAP2K7 mitogen-activated protein kinase kinase 7
NFATC2 nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2
NOS2 nitric oxide synthase 2, inducible
PNKD paroxysmal nonkinesigenic dyskinesia
PPARG peroxisome proliferator-activated receptor gamma
PRKCI protein kinase C, iota
PROM1 prominin 1
SIX1 SIX homeobox 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SQSTM1 sequestosome 1
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TPH2 tryptophan hydroxylase 2
VIM vimentin