anosmia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An inability to perceive odors. This is a general term describing inability to smell arising in any part of the process of smelling from absorption of odorants into the nasal mucous overlying the olfactory epithelium, diffusion to the cilia, binding to olfactory receptor sites, generation of action potentials in olfactory neurons, and perception of a smell. (Human Phenotype Ontology, HP_0000458)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000458
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ANOS1 anosmin 1
ARSE arylsulfatase E (chondrodysplasia punctata 1)
ATP13A2 ATPase type 13A2
CHD7 chromodomain helicase DNA binding protein 7
DNAI1 dynein, axonemal, intermediate chain 1
FEZF1 FEZ family zinc finger 1
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
MFN2 mitofusin 2
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PHYH phytanoyl-CoA 2-hydroxylase
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
SCN9A sodium channel, voltage gated, type IX alpha subunit
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SHH sonic hedgehog
SOX10 SRY (sex determining region Y)-box 10
TAC3 tachykinin 3
WDR11 WD repeat domain 11