| Approved symbol | UFM1 |
|---|---|
| Approved name | ubiquitin fold modifier 1 |
| HGCN ID | HGNC:20597 |
| Previous symbols | C13orf20 |
| Inheritance | |
| OMIM | 610553 |
| Chromosome | 13q13.3 |
| Panel(s) |
NGS Intellectual disability NGS Mendeliome NGS Microcephaly NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders NGS White matter disease UFM1 Select exon sequencing |
