disorganized retinal inner 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 which contains the cell bodies of bipolar, horizontal, and amacrine cells (Mammalian Phenotype Ontology, MP_0008512)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008512
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10 gene mutations causing the disorganized retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIC3 acid sensing (proton gated) ion channel 3
DSCAM Down syndrome cell adhesion molecule
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
RPL24 ribosomal protein L24
RS1 retinoschisin 1
SIRT1 sirtuin 1
VLDLR very low density lipoprotein receptor