optic nerve degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description retrogressive pathologic change of the optic nerve (Mammalian Phenotype Ontology, MP_0006219)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006219
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Genes

7 gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANK2 ankyrin 2, neuronal
ATP8A2 ATPase, aminophospholipid transporter, class I, type 8A, member 2
NR2E1 nuclear receptor subfamily 2, group E, member 1
SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3
TDRD7 tudor domain containing 7
TP53 tumor protein p53