zonular cataract Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Zonular cataracts are defined to be cataracts that affect specific regions of the lens. (Human Phenotype Ontology, HP_0010920)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010920
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18 genes associated with the zonular cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BEST1 bestrophin 1
BFSP1 beaded filament structural protein 1, filensin
CRYBA1 crystallin, beta A1
CRYBA4 crystallin, beta A4
CRYBB1 crystallin, beta B1
CRYBB2 crystallin, beta B2
CRYBB3 crystallin, beta B3
CRYGC crystallin, gamma C
FTL ferritin, light polypeptide
GJA3 gap junction protein, alpha 3, 46kDa
GJA8 gap junction protein, alpha 8, 50kDa
HSF4 heat shock transcription factor 4
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
OCRL oculocerebrorenal syndrome of Lowe
SEC23A Sec23 homolog A (S. cerevisiae)
VIM vimentin
WFS1 Wolfram syndrome 1 (wolframin)