C57BL/6J-Polgem1H/H
| Status | Available to order |
| EMMA ID | EM:14641 |
| Citation information | RRID:IMSR_EM:14641 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/6J-Polgem1H/H |
| Alternative name | POLG-A449T-EM1-B6 |
| Strain type | Endonuclease-mediated |
| Allele/Transgene symbol | Polgem1H |
| Gene/Transgene symbol | Polg |
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:not knownHeterozygous:None reported |
| Breeding history | Co-isogenic on original background |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| Homozygous matings required | not known |
| 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
- Alpers-Huttenlocher syndrome / Orphanet_726
- Spinocerebellar ataxia with epilepsy / Orphanet_254881
- Autosomal dominant progressive external ophthalmoplegia / Orphanet_254892
- Mitochondrial neurogastrointestinal encephalomyopathy / Orphanet_298
- Recessive mitochondrial ataxia syndrome / Orphanet_94125
- Sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome / Orphanet_70595
- Autosomal recessive progressive external ophthalmoplegia / Orphanet_254886