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
Similar Terms
Downloads & Tools

Genes

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