absent optic nerve Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the second cranial nerve which is responsible for conveying visual information from the retina to the brain (Mammalian Phenotype Ontology, MP_0001333)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001333
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11 gene mutations causing the absent optic nerve phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
BMP4 bone morphogenetic protein 4
GLI3 GLI family zinc finger 3
MITF microphthalmia-associated transcription factor
RPL24 ribosomal protein L24
SIX6 SIX homeobox 6
SLX4 SLX4 structure-specific endonuclease subunit
SMOC1 SPARC related modular calcium binding 1
TFAM transcription factor A, mitochondrial
TP53 tumor protein p53
VSX2 visual system homeobox 2