Episcleritis Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Inflammation of the episclera, a thin layer of tissue covering the white part (sclera) of the eye. (Human Phenotype Ontology, HP_0100534)
External Link https://www.disgenet.org/browser/0/1/0/C0014583
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Genes

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

Symbol Name
DBR1 debranching RNA lariats 1
DNASE1L3 deoxyribonuclease I-like 3
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
INSRR insulin receptor-related receptor
MBTPS2 membrane-bound transcription factor peptidase, site 2
NLRP3 NLR family, pyrin domain containing 3
PSMB8 proteasome (prosome, macropain) subunit, beta type, 8
RBM45 RNA binding motif protein 45
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3