upper respiratory tract disease Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A respiratory system disease which involves the upper respiratory tract. (Human Disease Ontology, DOID_974)
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12 genes associated with the disease upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
C11ORF30 chromosome 11 open reading frame 30 0.52461
SLC25A46 solute carrier family 25, member 46 0.52461
ENTPD6 ectonucleoside triphosphate diphosphohydrolase 6 (putative) 0.256228
IL2 interleukin 2 0.256228
CLEC16A C-type lectin domain family 16, member A 0.256228
EPS15 epidermal growth factor receptor pathway substrate 15 0.197766
GLI3 GLI family zinc finger 3 0.197766
DNAH5 dynein, axonemal, heavy chain 5 0.15771
TMEM108 transmembrane protein 108 0.15771
CROCC ciliary rootlet coiled-coil, rootletin 0.126165
TSLP thymic stromal lymphopoietin 0.100789
ABL2 ABL proto-oncogene 2, non-receptor tyrosine kinase 0.100789