B6.129-Sod1em2.2(SOD1*G93A)Emcf/H
| Status | Available to order |
| EMMA ID | EM:15896 |
| Citation information | RRID:IMSR_EM:15896 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 | B6.129-Sod1em2.2(SOD1*G93A)Emcf/H |
| Alternative name | Sod1 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Sod1em2.2(SOD1*G93A)Emcf |
| Gene/Transgene symbol | Sod1 |
Information from provider
| Provider | Elizabeth Fisher |
| Provider affiliation | Neuromuscular Diseases, UCL Queen Square Institute of Neurology |
| Genetic information | This strain carries a humanized mutant SOD1 allele with a G93A mutation. |
| Breeding history | Congenic on B6J. Originated on (129X1/SvJ x 129S1/Sv)F1-Kitl+. Injected egg cell background- C57BL/6J |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Amyotrophic lateral sclerosis / Orphanet_803