recurrent bronchitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increased susceptibility to bronchitis as manifested by a history of recurrent bronchitis. (Human Phenotype Ontology, HP_0002837)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002837
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Genes

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

Symbol Name
ATM ATM serine/threonine kinase
C1R complement component 1, r subcomponent
CD79A CD79a molecule, immunoglobulin-associated alpha
CD79B CD79b molecule, immunoglobulin-associated beta
DNAAF1 dynein, axonemal, assembly factor 1
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
MGP matrix Gla protein
NBN nibrin
RPGR retinitis pigmentosa GTPase regulator
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