| Primary Identifier | MGI:6441508 | Allele Type | Targeted |
| Attribute String | Humanized sequence | Gene | Scamp5 |
| Transmission | Germline | Strain of Origin | Not Specified |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | An arginine to tryptophan substitution at amino acid 91 (p.R91W) was introduced via homologous recombination. This mutation was identified in a Chinese consanguineous family with pediatric epilepsy and juvenile Parkinsons disease. |