abnormality of parotid gland Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the parotid glands, which are the salivary glands that are located in the subcutaneous tissues of the face overlying the mandibular ramus and anterior and inferior to the external ear. (Human Phenotype Ontology, HP_0000197)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000197
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Genes

6 genes associated with the abnormality of parotid gland 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
TCOF1 Treacher Collins-Franceschetti syndrome 1
TP63 tumor protein p63