Endophthalmitis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A globe disease that is characterized by inflammation of the inside of the eye. (Human Disease Ontology, DOID_4692)
External Link https://www.disgenet.org/browser/0/1/0/C0014236
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Genes

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

Symbol Name
CARD9 caspase recruitment domain family, member 9
CCL18 chemokine (C-C motif) ligand 18 (pulmonary and activation-regulated)
CUL9 cullin 9
EFS embryonal Fyn-associated substrate
FAS Fas cell surface death receptor
HMGB1 high mobility group box 1
IFNG interferon, gamma
IL10 interleukin 10
IL1B interleukin 1, beta
IL6 interleukin 6
INSRR insulin receptor-related receptor
MYD88 myeloid differentiation primary response 88
NTM neurotrimin
PER2 period circadian clock 2
PRF1 perforin 1 (pore forming protein)
SLPI secretory leukocyte peptidase inhibitor
TICAM1 toll-like receptor adaptor molecule 1
TLR2 toll-like receptor 2
TLR4 toll-like receptor 4
TNF tumor necrosis factor
TRIM69 tripartite motif containing 69
VEGFA vascular endothelial growth factor A