| Approved symbol | SLC39A5 |
|---|---|
| Approved name | solute carrier family 39 member 5 |
| HGCN ID | HGNC:20502 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608730 |
| Chromosome | 12q13.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Retinitis pigmentosa NGS Vision disorder CSNB |
