Common Cold Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An upper respiratory tract disease which involves inflammation of the mucous membranes of the nose, throat, eyes, and eustachian tubes with watery then purulent discharge. This is an acute contagious disease caused by rhinoviruses, human parainfluenza viruses, human respiratory syncytial virus, influenza viruses, adenoviruses, enteroviruses, or metapneumovirus. (Human Disease Ontology, DOID_10459)
External Link https://www.disgenet.org/browser/0/1/0/C0009443
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Genes

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

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
AQP4 aquaporin 4
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CXCL10 chemokine (C-X-C motif) ligand 10
DUSP10 dual specificity phosphatase 10
GCG glucagon
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
ICAM1 intercellular adhesion molecule 1
IFIH1 interferon induced with helicase C domain 1
IL13 interleukin 13
IL6 interleukin 6
LDLR low density lipoprotein receptor
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NANOS2 nanos homolog 2 (Drosophila)
NOS2 nitric oxide synthase 2, inducible
P2RY12 purinergic receptor P2Y, G-protein coupled, 12
PLA2G16 phospholipase A2, group XVI
SARS1 seryl-tRNA synthetase 1
SARS2 seryl-tRNA synthetase 2, mitochondrial
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5
SLC26A4 solute carrier family 26 (anion exchanger), member 4