pharynx cancer Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A gastrointestinal system cancer that is located_in the pharyx. (Human Disease Ontology, DOID_0060119)
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Genes

11 genes associated with the disease pharynx cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
HLA-C major histocompatibility complex, class I, C 1.83302
HLA-A major histocompatibility complex, class I, A 1.35663
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1 1.27521
HLA-J major histocompatibility complex, class I, J (pseudogene) 0.7623
TNFRSF19 tumor necrosis factor receptor superfamily, member 19 0.602429
MECOM MDS1 and EVI1 complex locus 0.52461
IER3 immediate early response 3 0.486425
ITGA9 integrin, alpha 9 0.4215
BLACE B-cell acute lymphoblastic leukemia expressed 0.274608
WLS wntless Wnt ligand secretion mediator 0.197766
HS3ST4 heparan sulfate (glucosamine) 3-O-sulfotransferase 4 0.043246