| Approved symbol | ORC1 |
|---|---|
| Approved name | origin recognition complex subunit 1 |
| HGCN ID | HGNC:8487 |
| Previous symbols | ORC1L |
| Inheritance | |
| OMIM | 601902 |
| Chromosome | 1p32.3 |
| Panel(s) |
NGS Intellectual disability NGS Mendelioom NGS Microcefalie NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Skeletdysplasie |
