punctate opacification of the cornea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Punctate opacification (reduced transparency) of the corneal stroma. (Human Phenotype Ontology, HP_0007856)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007856
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Genes

4 genes associated with the punctate opacification of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHST6 carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 6
KRT12 keratin 12, type I
KRT3 keratin 3, type II
UBIAD1 UbiA prenyltransferase domain containing 1