| Approved symbol | MFN2 |
|---|---|
| Approved name | mitofusin 2 |
| HGCN ID | HGNC:16877 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608507 |
| Chromosome | 1p36.22 |
| Panel(s) |
MFN2 Analysis NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Neuropathy/Charcot Marie Tooth NGS Optic atrophy NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Vision disorder CSNB |
