| Dataset | MPO Gene-Phenotype Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | abnormal accumulation of material on the retina (Mammalian Phenotype Ontology, MP_0006187) |
| External Link | http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006187 |
| Similar Terms | |
| Downloads & Tools |
7 gene mutations causing the retinal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol | Name |
|---|---|
| ABCC6 | ATP-binding cassette, sub-family C (CFTR/MRP), member 6 |
| CCL13 | chemokine (C-C motif) ligand 13 |
| CCR2 | chemokine (C-C motif) receptor 2 |
| CX3CR1 | chemokine (C-X3-C motif) receptor 1 |
| ENPP1 | ectonucleotide pyrophosphatase/phosphodiesterase 1 |
| TUB | tubby bipartite transcription factor |
| UBE3B | ubiquitin protein ligase E3B |
