Keratoglobus Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Limbus-to-limbus corneal thinning, often greatest in the periphery, with globular protrusion of the cornea. (Human Phenotype Ontology, HP_0001119)
External Link https://www.disgenet.org/browser/0/1/0/C3887531
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Genes

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

Symbol Name
COL1A1 collagen, type I, alpha 1
COL5A1 collagen, type V, alpha 1
COL5A2 collagen, type V, alpha 2
COL8A1 collagen, type VIII, alpha 1
COL8A2 collagen, type VIII, alpha 2
PIEZO2 piezo-type mechanosensitive ion channel component 2
PRDM5 PR domain containing 5
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
ZNF469 zinc finger protein 469