| 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 Mendelioom NGS Metabole aandoeningen NGS Microcefalie NGS Preconceptiepanel (t.b.v. consanguine paren) NGS Wittestofziekten UFM1 Select exon sequencing |
