retinal outer nuclear layer degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description a retrogressive impairment or destruction of the retinal layer that contains the nuclei and cell bodies of rods and cones (Mammalian Phenotype Ontology, MP_0008518)
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21 gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL3 ADP-ribosylation factor-like 3
ASIC3 acid sensing (proton gated) ion channel 3
ATP1B2 ATPase, Na+/K+ transporting, beta 2 polypeptide
ATXN7 ataxin 7
BBS1 Bardet-Biedl syndrome 1
CCL13 chemokine (C-C motif) ligand 13
CCR2 chemokine (C-C motif) receptor 2
CLCN2 chloride channel, voltage-sensitive 2
CRX cone-rod homeobox
GNGT1 guanine nucleotide binding protein (G protein), gamma transducing activity polypeptide 1
IL6 interleukin 6
NR2E3 nuclear receptor subfamily 2, group E, member 3
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PROM1 prominin 1
PRPH2 peripherin 2 (retinal degeneration, slow)
RDH13 retinol dehydrogenase 13 (all-trans/9-cis)
RHO rhodopsin
RPE65 retinal pigment epithelium-specific protein 65kDa
TUB tubby bipartite transcription factor
TULP1 tubby like protein 1
VLDLR very low density lipoprotein receptor