| Approved symbol | SP7 |
|---|---|
| Approved name | Sp7 transcription factor |
| HGCN ID | HGNC:17321 |
| Previous symbols | |
| Inheritance | |
| OMIM | 606633 |
| Chromosome | 12q13.13 |
| Panel(s) |
NGS Mendeliome NGS Osteogenesis imperfecta and related disorders NGS Osteopetrosis and dense bone dysplasia NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia |
