| Approved symbol | HK1 |
|---|---|
| Approved name | hexokinase 1 |
| HGCN ID | HGNC:4922 |
| Previous symbols | |
| Inheritance | |
| OMIM | 142600 |
| Chromosome | 10q22.1 |
| Panel(s) |
NGS Cone-rod dystrophy and macula degeneration NGS Hyperinsulinism NGS Intellectual disability NGS Leber’s congenital amaurosis LCA NGS Mendeliome NGS Movement disorders NGS Neuropathy/Charcot Marie Tooth NGS Preconception panel (for consanguineous couples) NGS Retinitis pigmentosa NGS Treatable metabolic neurodegenerative disorders NGS Vision disorder CSNB |
