increased corneal curvature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An increase in the degree of curvature of the cornea compared to normal. (Human Phenotype Ontology, HP_0100692)
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15 genes associated with the increased corneal curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
ANTXR1 anthrax toxin receptor 1
COL3A1 collagen, type III, alpha 1
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CRX cone-rod homeobox
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
LMX1B LIM homeobox transcription factor 1, beta
PIEZO2 piezo-type mechanosensitive ion channel component 2
PLOD1 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
PRDM5 PR domain containing 5
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SLC2A10 solute carrier family 2 (facilitated glucose transporter), member 10
VSX1 visual system homeobox 1
ZNF469 zinc finger protein 469