anxiety Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Feeling or dread, apprehension, and impending disaster. (Human Phenotype Ontology, HP_0000739)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000739
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Genes

37 genes associated with the anxiety phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADCY5 adenylate cyclase 5
ALDH5A1 aldehyde dehydrogenase 5 family, member A1
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CLN3 ceroid-lipofuscinosis, neuronal 3
CPOX coproporphyrinogen oxidase
DRD2 dopamine receptor D2
FMR1 fragile X mental retardation 1
GNAS GNAS complex locus
HMBS hydroxymethylbilane synthase
IGF1R insulin-like growth factor 1 receptor
JPH3 junctophilin 3
KPTN kaptin (actin binding protein)
MECP2 methyl CpG binding protein 2
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NKX2-1 NK2 homeobox 1
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
PAH phenylalanine hydroxylase
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PARK7 parkinson protein 7
PDE11A phosphodiesterase 11A
PDGFB platelet-derived growth factor beta polypeptide
PINK1 PTEN induced putative kinase 1
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PQBP1 polyglutamine binding protein 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRNP prion protein
PRRT2 proline-rich transmembrane protein 2
RRM2B ribonucleotide reductase M2 B (TP53 inducible)
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SGCE sarcoglycan, epsilon
TMCO1 transmembrane and coiled-coil domains 1
TTC19 tetratricopeptide repeat domain 19
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
WFS1 Wolfram syndrome 1 (wolframin)