| Approved symbol | KCNJ13 |
|---|---|
| Approved name | potassium inwardly rectifying channel subfamily J member 13 |
| HGCN ID | HGNC:6259 |
| Previous symbols | |
| Inheritance | |
| OMIM | 603208 |
| Chromosome | 2q37.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Stickler syndrome and related disorders NGS Vision disorder CSNB |
