| Primary Identifier | MGI:3783750 | Allele Type | Targeted |
| Attribute String | Null/knockout | Gene | Tpp2 |
| Transmission | Germline | Strain of Origin | 129S6/SvEvTac |
| Is Recombinase | false | Is Wild Type | false |
| description | Phenotypic Similarity to Human Syndrome: Evans Syndrome J:221205. |
| molecularNote | Exons 11 and 12 were removed by germ-line, cre-mediated recombination. The absence of protein activity was confirmed by an alanyl-alanyl-phenylalanyl-7-amino-4-methylcoumarin-degradation assay on splenocyte lysates and the absence of protein product was confirmed by western blot analysis on peripheral blood cell extracts. |
