abnormal optic nerve innervation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description misprojection or aberrant target finding of the second cranial nerve which is responsible for conveying visual information from the retina to the brain (Mammalian Phenotype Ontology, MP_0001332)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001332
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10 gene mutations causing the abnormal optic nerve innervation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DCC DCC netrin 1 receptor
EPHB1 EPH receptor B1
GAP43 growth associated protein 43
GPR143 G protein-coupled receptor 143
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
PAX2 paired box 2
POU4F2 POU class 4 homeobox 2
SCRIB scribbled planar cell polarity protein
VAX1 ventral anterior homeobox 1
VAX2 ventral anterior homeobox 2