| Approved symbol | IFT43 |
|---|---|
| Approved name | intraflagellar transport 43 |
| HGCN ID | HGNC:29669 |
| Previous symbols | C14orf179 |
| Inheritance | |
| OMIM | 614068 |
| Chromosome | 14q24.3 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Skeletal Dysplasia NGS Vision disorder CSNB |
