| Approved symbol | SLC39A14 |
|---|---|
| Approved name | solute carrier family 39 member 14 |
| HGCN ID | HGNC:20858 |
| Previous symbols | |
| Inheritance | |
| OMIM | 608736 |
| Chromosome | 8p21.3 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Osteopetrosis and dense bone dysplasia NGS Parkinson NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
