retina hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due an increased number of cells in the thin layer of neural tissue lining the back of the eyeball which contains visual receptors (Mammalian Phenotype Ontology, MP_0001329)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001329
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Genes

7 gene mutations causing the retina hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
DSCAM Down syndrome cell adhesion molecule
OTX1 orthodenticle homeobox 1
RYBP RING1 and YY1 binding protein
SAV1 salvador family WW domain containing protein 1
SOX2 SRY (sex determining region Y)-box 2
TGFB2 transforming growth factor, beta 2