Abnormality Of The Nasopharynx Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The nasopharynx (nasal part of the pharynx) lies behind the nose and above the level of the soft palate. (Human Phenotype Ontology, HP_0001739)
External Link https://www.disgenet.org/browser/0/1/0/C4025750
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Genes

10 genes associated with the disease Abnormality Of The Nasopharynx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
GJA1 gap junction protein, alpha 1, 43kDa
MATR3 matrin 3
MED12 mediator complex subunit 12
MID1 midline 1
SALL4 spalt-like transcription factor 4
SETBP1 SET binding protein 1
TP63 tumor protein p63