MGI phenotypes (gene matching)
- no abnormal phenotype detected / MGI
B6;129S7-Ufd1tm1Bld/Cnrm
| Status | Available to order |
| EMMA ID | EM:02203 |
| Citation information | RRID:IMSR_EM:02203 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | B6;129S7-Ufd1tm1Bld/Cnrm |
| Alternative name | ufd1l |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Ufd1tm1Bld |
| Gene/Transgene symbol | Ufd1 |
Information from provider
| Provider | Antonio BALDINI |
| Provider affiliation | institute of biosciences and technologies, Texas A&M health science center |
| Genetic information | A loxP site was inserted into the Ufd1l (Ufd1l) gene by homologous recombination in ES cells. The insertion replaced a 4.5kb fragment containing exons 2 and 3. The targeting generates a null allele. |
| Phenotypic information | None in heterozygotes. |
| Breeding history | Backcrossed to C57BL/6 for 3 generations. |
| References |
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Information from EMMA
| Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Literature references
- Congenital heart disease in mice deficient for the DiGeorge syndrome region.;Lindsay E A, Botta A, Jurecic V, Carattini-Rivera S, Cheah Y C, Rosenblatt H M, Bradley A, Baldini A, ;1999;Nature;401;379-83; 10517636