abnormality of the salivary glands Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010286
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Genes

15 genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLCN folliculin
GRHL3 grainyhead-like 3 (Drosophila)
IRF6 interferon regulatory factor 6
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NOD2 nucleotide-binding oligomerization domain containing 2
OGDH oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)
SOX10 SRY (sex determining region Y)-box 10
TCOF1 Treacher Collins-Franceschetti syndrome 1
TP63 tumor protein p63