subcapsular cataracts Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A cataract that affects the region of the lens directly beneath the capsule of the lens. (Human Phenotype Ontology, HP_0000523)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010251
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Genes

7 gene mutations causing the subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP4 bone morphogenetic protein 4
COL4A1 collagen, type IV, alpha 1
CRYBA2 crystallin, beta A2
CRYBB2 crystallin, beta B2
DMD dystrophin
RGN regucalcin
SPARC secreted protein, acidic, cysteine-rich (osteonectin)