| Primary Identifier | MGI:5706831 | Allele Type | Targeted |
| Attribute String | Conditional ready, Hypomorph | Gene | Senp2 |
| Transmission | Germline | Strain of Origin | Not Specified |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Sudden unexplained death in epilepsy J:217910. |
| molecularNote | A loxP site was inserted upstream of exon 13 and an FRT flanked neo cassette and loxP site were inserted downstream of exon 14 via homologous recombination. Real-time PCR and western blot analysis indicates a significant reduction in expression in the brain and heart of homozygous mice. |
