| Approved symbol | SLC17A5 |
|---|---|
| Approved name | solute carrier family 17 member 5 |
| HGCN ID | HGNC:10933 |
| Previous symbols | SIASD |
| Inheritance | |
| OMIM | 604322 |
| Chromosome | 6q13 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia NGS Treatable metabolic neurodegenerative disorders NGS White matter disease |
