bronchitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A bronchial disease that is an inflammation of the bronchial tubes. It is caused by bacteria and viruses. The disease has_symptom cough with mucus, has_symptom shortness of breath, has_symptom low fever and has_symptom chest tightness. (Human Disease Ontology, DOID_6132)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012387
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Genes

28 genes associated with the bronchitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
ATM ATM serine/threonine kinase
C1R complement component 1, r subcomponent
C21ORF59 chromosome 21 open reading frame 59
CCDC65 coiled-coil domain containing 65
CD79A CD79a molecule, immunoglobulin-associated alpha
CD79B CD79b molecule, immunoglobulin-associated beta
DNAAF1 dynein, axonemal, assembly factor 1
DNAAF5 dynein, axonemal, assembly factor 5
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
HYDIN HYDIN, axonemal central pair apparatus protein
ICOS inducible T-cell co-stimulator
IL2RG interleukin 2 receptor, gamma
LRRC6 leucine rich repeat containing 6
MGP matrix Gla protein
NBN nibrin
RPGR retinitis pigmentosa GTPase regulator
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit
SCNN1G sodium channel, non voltage gated 1 gamma subunit
SPAG1 sperm associated antigen 1
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TAPBP TAP binding protein (tapasin)
TNFRSF13B tumor necrosis factor receptor superfamily, member 13B
ZBTB24 zinc finger and BTB domain containing 24
ZMYND10 zinc finger, MYND-type containing 10