- no abnormal phenotype detected / MGI
B6;129S7-Ufd1tm1Bld/Cnrm
Status | Available to order |
EMMA ID | EM:02203 |
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
MGI phenotypes (gene matching)
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
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