Bruxism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A sleep disorder that involves involuntarily grinding or clenching of the teeth while sleeping. (Human Disease Ontology, DOID_2846)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D002012
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Genes

4 genes/proteins associated with the disease Bruxism from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
PRL prolactin 1.26021
DRD2 dopamine receptor D2 1.25557
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.25494
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.01062