thin retinal inner plexiform layer Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced thickness of the retinal cell layer where bipolar and amacrine cell axons synapse with ganglion cell dendrites (Mammalian Phenotype Ontology, MP_0008513)
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9 gene mutations causing the thin retinal inner plexiform layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ATOH7 atonal homolog 7 (Drosophila)
ATXN7 ataxin 7
HR hair growth associated
LRP5 low density lipoprotein receptor-related protein 5
MCOLN1 mucolipin 1
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
SEMA4A sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A