| Approved symbol | IFT122 |
|---|---|
| Approved name | intraflagellar transport 122 |
| HGCN ID | HGNC:13556 |
| Previous symbols | WDR10 |
| Inheritance | |
| OMIM | 606045 |
| Chromosome | 3q21.3-q22.1 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia |
