abnormal iris pigment epithelium Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the epithelial layer of the iris composed of cells containing pigment granules (Mammalian Phenotype Ontology, MP_0005199)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005199
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4 gene mutations causing the abnormal iris pigment epithelium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXC1 forkhead box C1
FOXC2 forkhead box C2
GPR143 G protein-coupled receptor 143
LYST lysosomal trafficking regulator