Bronchitis Gene Set

Dataset DISEASES Experimental Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
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)
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Genes

26 genes associated with the disease Bronchitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Symbol Name Standardized Value
FAM13A family with sequence similarity 13, member A 1.508
TIGD2 tigger transposable element derived 2 1.508
CHRNB4 cholinergic receptor, nicotinic, beta 4 (neuronal) 1.023
PSMA4 proteasome (prosome, macropain) subunit, alpha type, 4 1.023
CHRNA5 cholinergic receptor, nicotinic, alpha 5 (neuronal) 1.023
CHRNA3 cholinergic receptor, nicotinic, alpha 3 (neuronal) 1.023
HYKK hydroxylysine kinase 1.023
KLF11 Kruppel-like factor 11 0.971
CYS1 cystin 1 0.971
RRM2 ribonucleotide reductase M2 0.971
GRHL1 grainyhead-like 1 (Drosophila) 0.971
CAMK2D calcium/calmodulin-dependent protein kinase II delta 0.945
ARSJ arylsulfatase family, member J 0.945
POLR2L polymerase (RNA) II (DNA directed) polypeptide L, 7.6kDa 0.916
CRACR2B calcium release activated channel regulator 2B 0.916
PNPLA2 patatin-like phospholipase domain containing 2 0.916
TSPAN4 tetraspanin 4 0.916
CEND1 cell cycle exit and neuronal differentiation 1 0.916
TALDO1 transaldolase 1 0.916
RPLP2 ribosomal protein, large, P2 0.916
CD151 CD151 molecule (Raph blood group) 0.916
SLC25A22 solute carrier family 25 (mitochondrial carrier: glutamate), member 22 0.916
AP2A2 adaptor-related protein complex 2, alpha 2 subunit 0.916
CHID1 chitinase domain containing 1 0.916
PIDD1 p53-induced death domain protein 1 0.916
GATD1 glutamine amidotransferase class 1 domain containing 1 0.916