B6(129S1)-Del(7Sult1a1-Spn)6Yah/Orl
| Status | Available to order |
| EMMA ID | EM:06133 |
| Citation information | RRID:IMSR_EM:06133 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(129S1)-Del(7Sult1a1-Spn)6Yah/Orl |
| Alternative name | 16p11.2 del |
| Strain type | Targeted Mutant Strains : Other targeted |
| Allele/Transgene symbol | Del(7Sult1a1-Spn)6Yah |
| Gene/Transgene symbol | Del(7Sult1a1-Spn)6Yah |
Information from provider
| Provider | Thomas ARBOGAST |
| Provider affiliation | IGBMC |
| Genetic information | Deletion of 300 kb (25 genes from Spn to Sult1a1). |
| Phenotypic information | Unknown |
| Breeding history | Backcrossed 6-7 generations. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | yes |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | heterozygous C57BL/6NTac males |
Literature references
- Targeting the RHOA pathway improves learning and memory in adult Kctd13 and 16p11.2 deletion mouse models.;Martin Lorenzo Sandra, Nalesso Valérie, Chevalier Claire, Birling Marie-Christine, Herault Yann, ;2021;Molecular autism;12;1; 33436060
- Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.;Qiu Yuqi, Arbogast Thomas, Lorenzo Sandra Martin, Li Hongying, Tang Shih C, Richardson Ellen, Hong Oanh, Cho Shawn, Shanta Omar, Pang Timothy, Corsello Christina, Deutsch Curtis K, Chevalier Claire, Davis Erica E, Iakoucheva Lilia M, Herault Yann, Katsanis Nicholas, Messer Karen, Sebat Jonathan, ;2019;Cell reports;28;3320-3328.e4; 31553903
- Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes.;Arbogast Thomas, Ouagazzal Abdel-Mouttalib, Chevalier Claire, Kopanitsa Maksym, Afinowi Nurudeen, Migliavacca Eugenia, Cowling Belinda S, Birling Marie-Christine, Champy Marie-France, Reymond Alexandre, Herault Yann, ;2016;PLoS genetics;12;e1005709; 26872257
- Dissecting the autism-associated 16p11.2 locus identifies multiple drivers in neuroanatomical phenotypes and unveils a male-specific role for the major vault protein.;Kretz Perrine F, Wagner Christel, Mikhaleva Anna, Montillot Charlotte, Hugel Sylvain, Morella Ilaria, Kannan Meghna, Fischer Marie-Christine, Milhau Maxence, Yalcin Ipek, Brambilla Riccardo, Selloum Mohammed, Herault Yann, Reymond Alexandre, Collins Stephan C, Yalcin Binnaz, ;2023;Genome biology;24;261; 37968726
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