abnormal optic canal morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the short canal through the orbitosphenoid bone at the apex of the orbit that gives passage to the optic nerve and the opthalmic artery (Mammalian Phenotype Ontology, MP_0010704)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010704
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2 gene mutations causing the abnormal optic canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
RARB retinoic acid receptor, beta
RARG retinoic acid receptor, gamma