| Approved symbol | SLC52A2 |
|---|---|
| Approved name | solute carrier family 52 member 2 |
| HGCN ID | HGNC:30224 |
| Previous symbols | GPR172A |
| Inheritance | |
| OMIM | 607882 |
| Chromosome | 8q24.3 |
| Panel(s) |
NGS Fetal akinesia deformation sequence FADS NGS Mendeliome NGS Movement disorders NGS Muscle disorders NGS Neuropathy/Charcot Marie Tooth NGS Optic atrophy NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
