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 |