| Approved symbol | SLC35C1 |
|---|---|
| Approved name | solute carrier family 35 member C1 |
| HGCN ID | HGNC:20197 |
| Previous symbols | |
| Inheritance | |
| OMIM | 605881 |
| Chromosome | 11p11.2 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS Skeletal Dysplasia NGS Treatable metabolic neurodegenerative disorders |
