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 dystrophie en macula degeneratie NGS Dominante opticus atrofie NGS Intellectual disability NGS Leber congenital amaurosis LCA NGS Mendelioom NGS Retinitis pigmentosa NGS Visus pakket Retinale genen |