neoplasm of the oral cavity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tumor (abnormal growth of tissue) of the oral cavity. (Human Phenotype Ontology, HP_0100649)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100649
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Genes

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

Symbol Name
APC adenomatous polyposis coli
FLCN folliculin
HSPG2 heparan sulfate proteoglycan 2
KAT6B K(lysine) acetyltransferase 6B
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
OCRL oculocerebrorenal syndrome of Lowe
OFD1 oral-facial-digital syndrome 1
PTCH1 patched 1
PTCH2 patched 2
SOX10 SRY (sex determining region Y)-box 10
SUFU suppressor of fused homolog (Drosophila)
WRN Werner syndrome, RecQ helicase-like