thin retinal inner nuclear layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the retinal layer which contains the cell bodies of bipolar, horizontal, and amacrine cells (Mammalian Phenotype Ontology, MP_0008511)
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27 gene mutations causing the thin retinal inner nuclear layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ATOH7 atonal homolog 7 (Drosophila)
BARHL2 BarH-like homeobox 2
BHLHE22 basic helix-loop-helix family, member e22
BMP4 bone morphogenetic protein 4
CLCN7 chloride channel, voltage-sensitive 7
FKRP fukutin related protein
FSCN2 fascin actin-bundling protein 2, retinal
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
LAMA1 laminin, alpha 1
LARGE like-glycosyltransferase
LGR4 leucine-rich repeat containing G protein-coupled receptor 4
LHFPL2 lipoma HMGIC fusion partner-like 2
MAB21L1 mab-21-like 1 (C. elegans)
MCOLN1 mucolipin 1
MDM1 Mdm1 nuclear protein homolog (mouse)
NPHP4 nephronophthisis 4
NR2E1 nuclear receptor subfamily 2, group E, member 1
OTX2 orthodenticle homeobox 2
PFDN5 prefoldin subunit 5
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POU4F2 POU class 4 homeobox 2
RORB RAR-related orphan receptor B
RPL24 ribosomal protein L24
SEMA4A sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
SOD2 superoxide dismutase 2, mitochondrial
TRIM2 tripartite motif containing 2