Nocturnal Enuresis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Enuresis occurring during sleeping hours. (Human Phenotype Ontology, HP_0010677)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D053206
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Genes

18 genes/proteins associated with the disease Nocturnal Enuresis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ENUR1 enuresis, nocturnal 1 2.88009
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.4449
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6 1.3973
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.37332
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.24307
BDNF brain-derived neurotrophic factor 1.21984
GDPD3 glycerophosphodiester phosphodiesterase domain containing 3 1.20913
CASP3 caspase 3, apoptosis-related cysteine peptidase 1.20622
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled 1.19379
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.13929
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19 1.09927
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2 1.08655
ARC activity-regulated cytoskeleton-associated protein 1.07696
INHBE inhibin, beta E 1.0637
CREB1 cAMP responsive element binding protein 1 1.03827
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3 1.02188
TAGLN transgelin 1.0204
CASP7 caspase 7, apoptosis-related cysteine peptidase 1.01587