eye opacity Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description changes in the eye grossly observed as a milky or cloudy appearance that may be progressive and persistent throughout life (Mammalian Phenotype Ontology, MP_0009859)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009859
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7 gene mutations causing the eye opacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
ASXL1 additional sex combs like transcriptional regulator 1
FOXC2 forkhead box C2
PAX6 paired box 6
PDGFRB platelet-derived growth factor receptor, beta polypeptide
RAD23B RAD23 homolog B (S. cerevisiae)
SPNS2 spinster homolog 2 (Drosophila)