abnormal optic tract morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the paired bands of optic nerve fibers running from the optic chiasma mostly to the lateral geniculate body, with a smaller number of fibers terminating in the superior colliculus and the pretectal region (Mammalian Phenotype Ontology, MP_0004267)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004267
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Genes

10 gene mutations causing the abnormal optic tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3B1 adaptor-related protein complex 3, beta 1 subunit
ATOH7 atonal homolog 7 (Drosophila)
CACNB3 calcium channel, voltage-dependent, beta 3 subunit
EPHB1 EPH receptor B1
EPHB2 EPH receptor B2
GAP43 growth associated protein 43
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
PAX2 paired box 2
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5