increased corneal light-scattering Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the normal transmission of light through the cornea; light is reflected or absorbed instead; often due to anomalies in the arrangement of lamella in the corneal stroma (Mammalian Phenotype Ontology, MP_0003096)
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2 gene mutations causing the increased corneal light-scattering phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BFSP2 beaded filament structural protein 2, phakinin
LUM lumican