abnormal retinal rod bipolar cell morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the bipolar cells that function in low light and transmit signals only through amacrine cells (Mammalian Phenotype Ontology, MP_0006074)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006074
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Genes

16 gene mutations causing the abnormal retinal rod bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATOH7 atonal homolog 7 (Drosophila)
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)
DSCAML1 Down syndrome cell adhesion molecule like 1
FAT3 FAT atypical cadherin 3
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3
RELN reelin
SLC4A3 solute carrier family 4 (anion exchanger), member 3
SSTR1 somatostatin receptor 1
SSTR2 somatostatin receptor 2
TLR4 toll-like receptor 4