REM Sleep Behavior Disorder Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A sleep disorder that involves abnormal behavior including the acting out of violent or dramatic dreams during the sleep phase with rapid eye movement. (Human Disease Ontology, DOID_9091)
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11 genes/proteins associated with the disease REM Sleep Behavior Disorder from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.60058
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.29843
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.27905
BDNF brain-derived neurotrophic factor 1.26576
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.23042
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.19868
DRD2 dopamine receptor D2 1.09786
CASP7 caspase 7, apoptosis-related cysteine peptidase 1.05972
NR0B2 nuclear receptor subfamily 0, group B, member 2 1.04465
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 1.02933
FNDC4 fibronectin type III domain containing 4 1.02299