| Primary Identifier | MGI:2682372 | Allele Type | Targeted |
| Attribute String | Not Specified | Gene | Pdgfrb |
| Transmission | Germline | Strain of Origin | 129S4/SvJaeSor |
| Is Recombinase | false | Is Wild Type | false |
| molecularNote | A point mutation was engineered and incorporated in codon 770 of the endogenous locus via homologous recombination. The mutation results in a tyrosine to phenylalanine substitution (Y770F) at a site crucial for RasGAP signal transduction. |