| Approved symbol | COX10 |
|---|---|
| Approved name | cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 |
| HGCN ID | HGNC:2260 |
| Previous symbols | |
| Inheritance | |
| OMIM | 602125 |
| Chromosome | 17p12 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS White matter disease |
