| Approved symbol | SOX11 |
|---|---|
| Approved name | SRY-box transcription factor 11 |
| HGCN ID | HGNC:11191 |
| Previous symbols | |
| Inheritance | |
| OMIM | 600898 |
| Chromosome | 2p25.2 |
| Panel(s) |
NGS Cornelia de Lange syndrome NGS Intellectual disability NGS Mendeliome NGS Microcephaly |
