| Approved symbol | IFITM5 |
|---|---|
| Approved name | interferon induced transmembrane protein 5 |
| HGCN ID | HGNC:16644 |
| Previous symbols | |
| Inheritance | |
| OMIM | 614757 |
| Chromosome | 11p15.5 |
| Panel(s) |
NGS Mendeliome NGS Osteogenesis imperfecta and related disorders NGS Osteopetrosis and dense bone dysplasia NGS Skeletal Dysplasia |
