| Approved symbol | KMT2A |
|---|---|
| Approved name | lysine methyltransferase 2A |
| HGCN ID | HGNC:7132 |
| Previous symbols | MLL |
| Inheritance | |
| OMIM | 159555 |
| Chromosome | 11q23.3 |
| Panel(s) |
NGS Congenital Heart Defects NGS Cornelia de Lange syndrome NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Primary immunodeficiency PID NGS Skeletal Dysplasia NGS Treatable metabolic neurodegenerative disorders |
