B6J.129S2-Esrrbtm1.1Ics/Ics
| Status | Available to order |
| EMMA ID | EM:12971 |
| Citation information | RRID:IMSR_EM:12971 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 | B6J.129S2-Esrrbtm1.1Ics/Ics |
| Alternative name | ERR2 CM |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Esrrbtm1.1Ics |
| Gene/Transgene symbol | Esrrb |
Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
| Phenotypic information | Homozygous: NA Heterozygous: NA |
| Breeding history | 5 backcross generations |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | no |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic sensorineural deafness type DFNB / Orphanet_90636