panic disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An anxiety disorder that is characterized by unexpected and repeated episodes of intense fear accompanied by physical symptoms that may include chest pain, heart palpitations, shortness of breath, dizziness, or abdominal distress. (Human Disease Ontology, DOID_594)
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16 genes associated with the disease panic disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ANO2 anoctamin 2, calcium activated chloride channel 0.572184
PKP1 plakophilin 1 0.438544
SDK2 sidekick cell adhesion molecule 2 0.368757
CALCOCO1 calcium binding and coiled-coil domain 1 0.345945
SOX21 SRY (sex determining region Y)-box 21 0.345945
PLEKHG1 pleckstrin homology domain containing, family G (with RhoGef domain) member 1 0.311576
CLU clusterin 0.285417
KCNA3 potassium channel, voltage gated shaker related subfamily A, member 3 0.256228
GRM7 glutamate receptor, metabotropic 7 0.197766
ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif, 20 0.126165
CPT1C carnitine palmitoyltransferase 1C 0.126165
TNFRSF21 tumor necrosis factor receptor superfamily, member 21 0.100789
SMOX spermine oxidase 0.080593
FAM174A family with sequence similarity 174, member A 0.080593
RAN RAN, member RAS oncogene family 0.064973
USP25 ubiquitin specific peptidase 25 0.043246