| Approved symbol | COA8 |
|---|---|
| Approved name | cytochrome c oxidase assembly factor 8 |
| HGCN ID | HGNC:20492 |
| Previous symbols | C14orf153, APOPT1 |
| Inheritance | |
| OMIM | 616003 |
| Chromosome | 14q32.33 |
| Panel(s) |
NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS White matter disease |
