| Approved symbol | SATB2 |
|---|---|
| Approved name | SATB homeobox 2 |
| HGCN ID | HGNC:21637 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608148 |
| Chromosome | 2q33.1 |
| Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Skeletdysplasie |
| Approved symbol | SATB2 |
|---|---|
| Approved name | SATB homeobox 2 |
| HGCN ID | HGNC:21637 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608148 |
| Chromosome | 2q33.1 |
| Panel(s) |
NGS Epilepsie NGS Intellectual disability NGS Mendelioom NGS Skeletdysplasie |