| Approved symbol | SLC25A46 |
|---|---|
| Approved name | solute carrier family 25 member 46 |
| HGCN ID | HGNC:25198 |
| Previous symbols | |
| Inheritance | |
| OMIM | 610826 |
| Chromosome | 5q22.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Neuropathy/Charcot Marie Tooth NGS Optic atrophy NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
