| Approved symbol | ALG11 |
|---|---|
| Approved name | ALG11 alpha-1,2-mannosyltransferase |
| HGCN ID | HGNC:32456 |
| Previous symbols | |
| Inheritance | |
| OMIM | 613666 |
| Chromosome | 13q14.3 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
