MGI phenotypes (gene matching)
- no phenotypic analysis / MGI
B6.129S7-Ess2tm1Bld/Cnrm
| Status | Available to order |
| EMMA ID | EM:02204 |
| Citation information | RRID:IMSR_EM:02204 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-Ess2tm1Bld/Cnrm |
| Alternative name | ES2 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Ess2tm1Bld |
| Gene/Transgene symbol | Ess2 |
Information from provider
| Provider | Antonio BALDINI |
| Provider affiliation | institute of biosciences and technologies, Texas A&M health science center |
| Genetic information | The gene was inactivated by homologous recombination in ES cells by replacing a 200bp fragment of exon 4 with an artificial construct comprising: PGK promoter, 2 exons of HPRT minigene, LoxP site, PolII, neo cassette. The targeting generates a null allele. |
| Phenotypic information | None in heterozygotes. |
| 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