abnormal optic eminence morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the embryonic structure that gives rise to the corneal ectoderm (Mammalian Phenotype Ontology, MP_0006305)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006305
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2 gene mutations causing the abnormal optic eminence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
OVOL2 ovo-like zinc finger 2