Upper Airway Obstruction Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Increased resistance to the passage of air in the upper airway. (Human Phenotype Ontology, HP_0002781)
External Link https://www.disgenet.org/browser/0/1/0/C0740852
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Genes

15 genes associated with the disease Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BTNL2 butyrophilin-like 2
CDK13 cyclin-dependent kinase 13
CLASP1 cytoplasmic linker associated protein 1
COL11A1 collagen, type XI, alpha 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GHRH growth hormone releasing hormone
GHRHR growth hormone releasing hormone receptor
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
POR P450 (cytochrome) oxidoreductase
SH3BP2 SH3-domain binding protein 2
SOX9 SRY (sex determining region Y)-box 9
ZSWIM6 zinc finger, SWIM-type containing 6