| Approved symbol | SLC2A1 |
|---|---|
| Approved name | solute carrier family 2 member 1 |
| HGCN ID | HGNC:11005 |
| Previous symbols | GLUT1, GLUT, HTLVR, CSE |
| Inheritance | |
| OMIM | 138140 |
| Chromosome | 1p34.2 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders |
