Agoraphobia Gene Set

Dataset DisGeNET 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 https://www.disgenet.org/browser/0/1/0/C3264595
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Genes

27 genes associated with the disease Agoraphobia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADORA2A adenosine A2a receptor
BDNF brain-derived neurotrophic factor
CAMKK2 calcium/calmodulin-dependent protein kinase kinase 2, beta
CREBBP CREB binding protein
CRH corticotropin releasing hormone
CRP C-reactive protein, pentraxin-related
EP300 E1A binding protein p300
GAD1 glutamate decarboxylase 1 (brain, 67kDa)
GLRB glycine receptor, beta
GRP gastrin-releasing peptide
GRPR gastrin-releasing peptide receptor
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR1 hypocretin (orexin) receptor 1
HTR1A 5-hydroxytryptamine (serotonin) receptor 1A, G protein-coupled
KRT7 keratin 7, type II
MAOA monoamine oxidase A
NPSR1 neuropeptide S receptor 1
NPY neuropeptide Y
OPN1SW opsin 1 (cone pigments), short-wave-sensitive
P2RX7 purinergic receptor P2X, ligand gated ion channel, 7
SCLY selenocysteine lyase
SGCE sarcoglycan, epsilon
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
SLC6A4 solute carrier family 6 (neurotransmitter transporter), member 4
TAL1 T-cell acute lymphocytic leukemia 1
TPH2 tryptophan hydroxylase 2