| 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 dystrophie en macula degeneratie NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Retinitis pigmentosa NGS Stickler syndroom en gerelateerde aandoeningen NGS Visus pakket Retinale genen |
