Nasopharyngitis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A nasopharyngeal disease which involves inflammation of the nasal passages and upper part of the pharynx. (Human Disease Ontology, DOID_10460)
External Link https://www.disgenet.org/browser/0/1/0/C0027441
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Genes

17 genes associated with the disease Nasopharyngitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
AMELX amelogenin, X-linked
APCS amyloid P component, serum
BCR breakpoint cluster region
CD163 CD163 molecule
DPP4 dipeptidyl-peptidase 4
E2F2 E2F transcription factor 2
GRIN2A glutamate receptor, ionotropic, N-methyl D-aspartate 2A
LRRC4 leucine rich repeat containing 4
MAP3K5 mitogen-activated protein kinase kinase kinase 5
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
PDLIM7 PDZ and LIM domain 7 (enigma)
PLAC8 placenta-specific 8
PPARA peroxisome proliferator-activated receptor alpha
PTH parathyroid hormone
VIM vimentin