disorganized retinal ganglion layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the pattern of the innermost nuclear layer of the retina, which contains neurons that project axons through the optic nerve to the brain (Mammalian Phenotype Ontology, MP_0008509)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008509
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5 gene mutations causing the disorganized retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCND1 cyclin D1
DSCAM Down syndrome cell adhesion molecule
LARGE like-glycosyltransferase
NDP Norrie disease (pseudoglioma)
NR2E1 nuclear receptor subfamily 2, group E, member 1