retinal pigment epithelium hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increased numbers of cells in the epithelial layer of the retina composed of cells containing pigment granules (Mammalian Phenotype Ontology, MP_0005549)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005549
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Genes

6 gene mutations causing the retinal pigment epithelium hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARHGAP35 Rho GTPase activating protein 35
GSK3A glycogen synthase kinase 3 alpha
MDM1 Mdm1 nuclear protein homolog (mouse)
OTX2 orthodenticle homeobox 2
SLC35F6 solute carrier family 35, member F6
SLC9A8 solute carrier family 9, subfamily A (NHE8, cation proton antiporter 8), member 8