| Primary Identifier | MGI:5752649 | Allele Type | Targeted |
| Attribute String | Hypomorph | Gene | Sprtn |
| Transmission | Germline | Strain of Origin | 129S/SvEv |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Progeria (J:225198) |
| molecularNote | A loxP site was inserted upstream of exon 2. An FRT-flanked neomycin resistance cassette with a 3' loxP site was inserted downstream of exon 2. RT-PCR confirmed reduced transcript expression due to the cryptic exon in the neomycin resistance cassette. |
