disorganized retinal outer nuclear layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description derangement of the normal pattern of the retinal layer that contains the nuclei and cell bodies of rods and cones (Mammalian Phenotype Ontology, MP_0008516)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008516
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Genes

11 gene mutations causing the disorganized retinal outer nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIC3 acid sensing (proton gated) ion channel 3
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LRP5 low density lipoprotein receptor-related protein 5
MAP1B microtubule-associated protein 1B
NR2E1 nuclear receptor subfamily 2, group E, member 1
NR2E3 nuclear receptor subfamily 2, group E, member 3
PRPH2 peripherin 2 (retinal degeneration, slow)
RHO rhodopsin
RPL24 ribosomal protein L24
RS1 retinoschisin 1
SIRT1 sirtuin 1