| 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 |
| Similar Terms | |
| Downloads & Tools |
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 |
