abnormal retinal bipolar cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cells that transmit signals from the photoreceptors to retinal amacrine and ganglion cells (Mammalian Phenotype Ontology, MP_0006073)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006073
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27 gene mutations causing the abnormal retinal bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
ATOH7 atonal homolog 7 (Drosophila)
BHLHE22 basic helix-loop-helix family, member e22
BHLHE23 basic helix-loop-helix family, member e23
CABP4 calcium binding protein 4
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CFH complement factor H
CNGB1 cyclic nucleotide gated channel beta 1
CRX cone-rod homeobox
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
DSCAM Down syndrome cell adhesion molecule
DSCAML1 Down syndrome cell adhesion molecule like 1
E2F1 E2F transcription factor 1
ERC2 ELKS/RAB6-interacting/CAST family member 2
FAT3 FAT atypical cadherin 3
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3
IRX5 iroquois homeobox 5
IRX6 iroquois homeobox 6
MYH10 myosin, heavy chain 10, non-muscle
NEUROD1 neuronal differentiation 1
OTX2 orthodenticle homeobox 2
RELN reelin
SLC4A3 solute carrier family 4 (anion exchanger), member 3
SSTR1 somatostatin receptor 1
SSTR2 somatostatin receptor 2
TLR4 toll-like receptor 4
VSX1 visual system homeobox 1