Corneal Erosion Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An erosion or abrasion of the cornea's outermost layer of epithelial cells. (Human Phenotype Ontology, HP_0200020)
External Link https://www.disgenet.org/browser/0/1/0/C0392163
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Genes

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

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
ALDH3A2 aldehyde dehydrogenase 3 family, member A2
ALOX12B arachidonate 12-lipoxygenase, 12R type
ALOXE3 arachidonate lipoxygenase 3
CERS3 ceramide synthase 3
COL17A1 collagen, type XVII, alpha 1
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
COL7A1 collagen, type VII, alpha 1
ELP1 elongator acetyltransferase complex subunit 1
FERMT1 fermitin family member 1
FGFR2 fibroblast growth factor receptor 2
FOXC2 forkhead box C2
FOXE3 forkhead box E3
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
HLA-B major histocompatibility complex, class I, B
IKZF1 IKAROS family zinc finger 1 (Ikaros)
KIFBP kinesin family binding protein
MBTPS2 membrane-bound transcription factor peptidase, site 2
MMP1 matrix metallopeptidase 1
NIPAL4 NIPA-like domain containing 4
PNPLA1 patatin-like phospholipase domain containing 1
PRDM5 PR domain containing 5
SLC39A4 solute carrier family 39 (zinc transporter), member 4
SPINT2 serine peptidase inhibitor, Kunitz type, 2
TGFBI transforming growth factor, beta-induced, 68kDa
TGM1 transglutaminase 1
TP63 tumor protein p63
TWIST2 twist family bHLH transcription factor 2
ZNF469 zinc finger protein 469