Approved symbol | SCO2 |
---|---|
Approved name | synthesis of cytochrome C oxidase 2 |
HGCN ID | HGNC:10604 |
Previous symbols | MYP6 |
Inheritance | |
OMIM | 604272 |
Chromosome | 22q13.33 |
Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Preconception panel (for consanguineous couples) NGS White matter disease |