Sleep Bruxism Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D020186
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Genes

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

Symbol Name Standardized Value
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase) 1.39952
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.32399
KCNJ3 potassium channel, inwardly rectifying subfamily J, member 3 1.27502
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6 1.27132
PRL prolactin 1.15324
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.14816
BDNF brain-derived neurotrophic factor 1.13586
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.13313
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5 1.03976