nuclear cataract Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A nuclear cataract is an opacity or clouding that develops in the lens nucleus. That is, a nuclear cataract is one that is located in the center of the lens. The nucleus tends to darken changing from clear to yellow and sometimes brown. (Human Phenotype Ontology, HP_0100018)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0100018
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Genes

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

Symbol	Name
CRYBB1	crystallin, beta B1
CRYBB3	crystallin, beta B3
CRYGC	crystallin, gamma C
FTL	ferritin, light polypeptide
GJA8	gap junction protein, alpha 8, 50kDa
HSF4	heat shock transcription factor 4
NHS	Nance-Horan syndrome (congenital cataracts and dental anomalies)
VIM	vimentin
WFS1	Wolfram syndrome 1 (wolframin)