Agoraphobia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A phobic disorder involving the specific anxiety about being in a place or situation where escape is difficult or embarrassing or where help may be unavailable. (Human Disease Ontology, DOID_593)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D000379
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Genes

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

Symbol Name Standardized Value
SLC22A2 solute carrier family 22 (organic cation transporter), member 2 1.27689
HTR2A 5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 1.25183
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 1.11151
BDNF brain-derived neurotrophic factor 1.10838
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4 1.09332
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4 1.06479
CRH corticotropin releasing hormone 1.03604