abnormal retinal inner plexiform layer morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the retinal cell layer where bipolar and amacrine cell axons synapse with ganglion cell dendrites (Mammalian Phenotype Ontology, MP_0003734)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003734
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23 gene mutations causing the abnormal retinal inner plexiform layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGTPBP1 ATP/GTP binding protein 1
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ATOH7 atonal homolog 7 (Drosophila)
ATXN7 ataxin 7
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CACNA2D4 calcium channel, voltage-dependent, alpha 2/delta subunit 4
DSCAM Down syndrome cell adhesion molecule
DSCAML1 Down syndrome cell adhesion molecule like 1
GDF11 growth differentiation factor 11
GPHN gephyrin
HR hair growth associated
IRX6 iroquois homeobox 6
LRP5 low density lipoprotein receptor-related protein 5
MCOLN1 mucolipin 1
NR2E1 nuclear receptor subfamily 2, group E, member 1
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PLXNA2 plexin A2
PTF1A pancreas specific transcription factor, 1a
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
SEMA6A sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A