| Approved symbol | RPGR |
|---|---|
| Approved name | retinitis pigmentosa GTPase regulator |
| HGCN ID | HGNC:10295 |
| Previous symbols | CRD, RP3, RP15, COD1 |
| Inheritance | |
| OMIM | 312610 |
| Chromosome | Xp11.4 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Primary ciliary dyskinesia PCD NGS Retinitis pigmentosa NGS Vision disorder CSNB RPGR Analysis |
