posterior subcapsular cataract Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A type of cataract affecting the posterior pole of lens immediately adjacent to ('beneath') the Lens capsule. (Human Phenotype Ontology, HP_0007787)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0007787
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Genes

8 genes associated with the posterior subcapsular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ADAMTS18	ADAM metallopeptidase with thrombospondin type 1 motif, 18
CHMP4B	charged multivesicular body protein 4B
CNBP	CCHC-type zinc finger, nucleic acid binding protein
IMPG2	interphotoreceptor matrix proteoglycan 2
NF2	neurofibromin 2 (merlin)
OAT	ornithine aminotransferase
OFD1	oral-facial-digital syndrome 1
RBP3	retinol binding protein 3, interstitial