C57BL/6NTac-Grm1em1H/H
| Status | Available to order |
| EMMA ID | EM:12530 |
| Citation information | RRID:IMSR_EM:12530 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 | C57BL/6NTac-Grm1em1H/H |
| Alternative name | GRM1-Y792C-EM1-B6N |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Grm1em1H |
| Gene/Transgene symbol | Grm1 |
Information from provider
| Provider | MRC-Harwell |
| Provider affiliation | Mary Lyon Centre at MRC Harwell |
| Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
| Phenotypic information | Homozygous:abnormal gait and ataxiaHeterozygous:abnormal gait and ataxia |
| Breeding history | Co-isogenic on original background |
| References | None available |
| Homozygous fertile | yes |
| Homozygous viable | not known |
| Homozygous matings required | no |
| Immunocompromised | not known |
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
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency / Orphanet_324262