Ehrlichiosis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A primary bacterial infectious disease that results_in infection located_in leukocyte, has_material_basis_in Ehrlichia chaffeensis or Anaplasma phagocytophilum, which are transmitted_by lone start stick and transmitted_by black-legged tick respectively. The infection has_symptom headache, has_symptom muscle aches, has_symptom fatigue and has_symptom rash. (Human Disease Ontology, DOID_10242)
External Link https://www.disgenet.org/browser/0/1/0/C0085399
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Genes

19 genes associated with the disease Ehrlichiosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
BCAP31 B-cell receptor-associated protein 31
DNALI1 dynein, axonemal, light intermediate chain 1
FSCN2 fascin actin-bundling protein 2, retinal
GC group-specific component (vitamin D binding protein)
GOSR1 golgi SNAP receptor complex member 1
GSTO1 glutathione S-transferase omega 1
HP haptoglobin
IL27 interleukin 27
MMP12 matrix metallopeptidase 12
MYD88 myeloid differentiation primary response 88
NOD2 nucleotide-binding oligomerization domain containing 2
PSMD10 proteasome (prosome, macropain) 26S subunit, non-ATPase, 10
RBP4 retinol binding protein 4, plasma
ROS1 ROS proto-oncogene 1 , receptor tyrosine kinase
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
TLR2 toll-like receptor 2
TLR9 toll-like receptor 9
TMED5 transmembrane emp24 protein transport domain containing 5