| Primary Identifier | MGI:7516157 | Allele Type | Endonuclease-mediated |
| Attribute String | Humanized sequence | Gene | Svep1 |
| Strain of Origin | C57BL/6 | Is Recombinase | false |
| Is Wild Type | false |
| molecularNote | Aspartic acid codon 2699 (GAT) in exon 38 was changed to glycine (GGT) (p.D2699G) using an sgRNA and an ssODN template with CRISPR/Cas9 technology. The mutation is the equivalent of the human p.D2702G mutation associated with coronary artery disease (CAD). |