Sutural Cataract Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of congenital cataract in which the opacity follows the anterior or posterior Y suture. (Human Phenotype Ontology, HP_0010695)
External Link https://www.disgenet.org/browser/0/1/0/C4023734
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Genes

5 genes associated with the disease Sutural Cataract in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BFSP2 beaded filament structural protein 2, phakinin
CRYBB2 crystallin, beta B2
GJA8 gap junction protein, alpha 8, 50kDa
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
SEC23A Sec23 homolog A (S. cerevisiae)