xerostomia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Dryness of the mouth due to salivary gland dysfunction. (Human Phenotype Ontology, HP_0000217)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000217
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Genes

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

Symbol Name
CAV1 caveolin 1, caveolae protein, 22kDa
CCR6 chemokine (C-C motif) receptor 6
CHRM3 cholinergic receptor, muscarinic 3
CTGF connective tissue growth factor
FERMT1 fermitin family member 1
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IRF5 interferon regulatory factor 5
LBR lamin B receptor
NOD2 nucleotide-binding oligomerization domain containing 2
SCN9A sodium channel, voltage gated, type IX alpha subunit
TP63 tumor protein p63