Tuberculosis Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A primary bacterial infectious disease that is located_in lungs, located_in lymph nodes, located_in pericardium, located_in brain, located_in pleura or located_in gastrointestinal tract, has_material_basis_in Mycobacterium tuberculosis, which is transmitted_by droplets released into the air when an infected person coughs or sneezes. (Human Disease Ontology, DOID_399)
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16 genes associated with the Tuberculosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1 0.342586
C2CD2 C2 calcium-dependent domain containing 2 0.314454
IL2RB interleukin 2 receptor, beta 0.314454
STXBP5 syntaxin binding protein 5 (tomosyn) 0.220915
PARD3B par-3 family cell polarity regulator beta 0.165905
DSCAM Down syndrome cell adhesion molecule 0.165905
DCUN1D5 DCN1, defective in cullin neddylation 1, domain containing 5 0.165905
ZFPM2 zinc finger protein, FOG family member 2 0.129504
DUSP14 dual specificity phosphatase 14 0.129504
NAA60 N(alpha)-acetyltransferase 60, NatF catalytic subunit 0.129504
NAV3 neuron navigator 3 0.104568
GMDS-AS1 GMDS antisense RNA 1 (head to head) 0.104568
ZNF229 zinc finger protein 229 0.104568
VWA8 von Willebrand factor A domain containing 8 0.085234
SPON1 spondin 1, extracellular matrix protein 0.042592
AHCYL2 adenosylhomocysteinase-like 2 0.042592