abnormal retinal nerve fiber layer morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the layer of the retina formed by expansion of the fibers of the optic nerve (Mammalian Phenotype Ontology, MP_0006303)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006303
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13 gene mutations causing the abnormal retinal nerve fiber layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASPA aspartoacylase
ATOH7 atonal homolog 7 (Drosophila)
FASLG Fas ligand (TNF superfamily, member 6)
GUCY1A3 guanylate cyclase 1, soluble, alpha 3
ITGA6 integrin, alpha 6
LRP5 low density lipoprotein receptor-related protein 5
NR2E1 nuclear receptor subfamily 2, group E, member 1
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PAX2 paired box 2
POU4F2 POU class 4 homeobox 2
SOD1 superoxide dismutase 1, soluble
TSPAN12 tetraspanin 12