abnormal optic chiasm morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the flattened quadrangular body that is the point of crossing of the fibers of the optic nerves (Mammalian Phenotype Ontology, MP_0009770)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009770
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7 gene mutations causing the abnormal optic chiasm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
GAP43 growth associated protein 43
GLI3 GLI family zinc finger 3
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
PAX2 paired box 2
SCRIB scribbled planar cell polarity protein
VAX1 ventral anterior homeobox 1