optic neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001138
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Genes

5 genes associated with the optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
CLCN2 chloride channel, voltage-sensitive 2
NOTCH3 notch 3
SH3BP2 SH3-domain binding protein 2
TSFM Ts translation elongation factor, mitochondrial