B6J.129S2-Nr5a1tm1.2Ics/Ics
| Status | Available to order |
| EMMA ID | EM:12984 |
| Citation information | RRID:IMSR_EM:12984 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-Nr5a1tm1.2Ics/Ics |
| Alternative name | SF1 KO |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Nr5a1tm1.2Ics |
| Gene/Transgene symbol | Nr5a1 |
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:not knownHeterozygous:not known |
| Breeding history | 7 backcross generations |
| References | None available |
| Homozygous fertile | not known |
| Homozygous viable | not known |
| 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
- 46,XX ovotesticular disorder of sex development / Orphanet_2138
- 46,XX testicular disorder of sex development / Orphanet_393
- Male infertility with azoospermia or oligozoospermia due to single gene mutation / Orphanet_399805
- 46,XY complete gonadal dysgenesis / Orphanet_242
- 46,XX gonadal dysgenesis / Orphanet_243
- 46,XY partial gonadal dysgenesis / Orphanet_251510