B6J.129S2-Nr2e3tm1.1Ics/Ics
| Status | Available to order |
| EMMA ID | EM:12962 |
| International strain name | B6J.129S2-Nr2e3tm1.1Ics/Ics |
| Alternative name | PNR CM |
| Strain type | Targeted Mutant Strains : Conditional mutation |
| Allele/Transgene symbol | Nr2e3tm1.1Ics |
| Gene/Transgene symbol | Nr2e3 |
Information from provider
| Provider | ICS, Institut Clinique de la Souris |
| Provider affiliation | ICS, Institut Clinique de la Souris |
| Genetic information | Region from exon 1 to exon 6 was flanked by loxP sites. An FRT site remains in intron from removal of the selection cassette. |
| Phenotypic information | Homozygous:NAHeterozygous:NA |
| Breeding history | 6 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
- Retinitis pigmentosa / Orphanet_791
- Goldmann-Favre syndrome / Orphanet_53540