Corneal Opacity Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A reduction of corneal clarity. (Human Phenotype Ontology, HP_0007957)
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6 genes associated with the Corneal Opacity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
FLNA filamin A, alpha
LCAT lecithin-cholesterol acyltransferase
PAX6 paired box 6
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)