| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | reduced thickness of the innermost nuclear layer of the retina, which contains neurons that project axons through the optic nerve to the brain (Mammalian Phenotype Ontology, MP_0008507) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008507 |
| Similar Terms | |
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10 gene mutations causing the thin retinal ganglion layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| BARHL2 | BarH-like homeobox 2 |
| BMP4 | bone morphogenetic protein 4 |
| CCND1 | cyclin D1 |
| FST | follistatin |
| HR | hair growth associated |
| LAMA1 | laminin, alpha 1 |
| OPA3 | optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) |
| PAX2 | paired box 2 |
| POU4F2 | POU class 4 homeobox 2 |
| RPL24 | ribosomal protein L24 |
