Primary Identifier | MGI:7628361 | Allele Type | Targeted |
Attribute String | Humanized sequence | Gene | Thbs4 |
Transmission | Germline | Strain of Origin | Not Specified |
Is Recombinase | false | Is Wild Type | false |
molecularNote | Alanine codon 389 (GCG) in exon 9 was changed to proline (CCG) (p.A389P). The mutation is the equivalent of the human p.A387P mutation associated with myocardial infarction (MI) and coronary artery disease (CAD). |