absent optic chiasm Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the flattened quadrangular body that is the point of crossing of the fibers of the optic nerves (Mammalian Phenotype Ontology, MP_0009771)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009771
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2 gene mutations causing the absent optic chiasm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
PAX2 paired box 2
VAX1 ventral anterior homeobox 1