brucellosis Gene Set

Dataset	GAD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A primary bacterial infectious disease that is caused by the bacteria of the genus Brucella, when humans come in contact with contaminated animals or animal products or ingestion of infected food products. The disease has_symptom fever, has_symptom sweat, has_symptom headache, has_symptom back pain, has_symptom physical weakness, has_symptom joint pain and has_symptom fatigue. (Human Disease Ontology, DOID_11077)
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Genes

17 genes associated with the disease brucellosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol	Name
CCR5	chemokine (C-C motif) receptor 5 (gene/pseudogene)
FCGR2A	Fc fragment of IgG, low affinity IIa, receptor (CD32)
IFNG	interferon, gamma
IL10	interleukin 10
IL1RN	interleukin 1 receptor antagonist
IL4	interleukin 4
IL6	interleukin 6
LMPH1B	Lymphedema, hereditary, IB
MICA	MHC class I polypeptide-related sequence A
PSMB8	proteasome (prosome, macropain) subunit, beta type, 8
PSMB9	proteasome (prosome, macropain) subunit, beta type, 9
SLC11A1	solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1
TAP1	transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2	transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TGFB1	transforming growth factor, beta 1
TLR4	toll-like receptor 4
TNF	tumor necrosis factor