| Approved symbol | PSAP |
|---|---|
| Approved name | prosaposin |
| HGCN ID | HGNC:9498 |
| Previous symbols | SAP1, GLBA, SAP2 |
| Inheritance | |
| OMIM | 176801 |
| Chromosome | 10q22.1 |
| Panel(s) |
NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Interstitial lung disease ILD NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Treatable metabolic neurodegenerative disorders NGS White matter disease |
