| Approved symbol | NR2F1 |
|---|---|
| Approved name | nuclear receptor subfamily 2 group F member 1 |
| HGCN ID | HGNC:7975 |
| Previous symbols | ERBAL3, TFCOUP1 |
| Inheritance | |
| OMIM | 132890 |
| Chromosome | 5q15 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Optic atrophy NGS Retinitis pigmentosa NGS Vision disorder CSNB |
