retinal gliosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased proliferation of neuroglia in a damaged area of the retina that may lead to the formation of scar tissue (Mammalian Phenotype Ontology, MP_0009392)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009392
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Genes

4 gene mutations causing the retinal gliosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CBS cystathionine-beta-synthase
PXDN peroxidasin
TSPAN12 tetraspanin 12