B6;129S7-Dp(16Dgcr14-Ufd1l)217Bld/Cnrm
Status | Available to order |
EMMA ID | EM:02121 |
International strain name | B6;129S7-Dp(16Dgcr14-Ufd1l)217Bld/Cnrm |
Alternative name | Dp(16)1_Bld |
Strain type | Targeted Mutant Strains : Other targeted |
Allele/Transgene symbol | Dp(16Dgcr14-Ufd1l)217Bld, |
Gene/Transgene symbol | Dp(16Dgcr14-Ufd1l)217Bld |
Information from provider
Provider | Antonio BALDINI |
Provider affiliation | Institute of Genetics and Biophysics (IGB), National Research Council (CNR) |
Genetic information | LoxP sites were inserted in trans into genes Es2 and Ufd1l; cre recombination in ES cells generated a chromosomal deletion named Df(16)1_Bld, and a chromosomal duplication named Dp(16)1_Bld. The two mutations were independently established in mice. |
Phenotypic information | There are no overt phenotypic abnormalities associated with this duplication, except for behavioral abnormalities (hyperactivity) not yet fully characterized. |
Breeding history | Backcrossed to C57BL/6 and then intercrossed; mixed 129 and C57BL/6 (ca. 75% C57BL/6) background. |
References |
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Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
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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