MGI phenotypes (gene matching)
B6;129P2-Prmt2tm1Yah/Orl
| Status | Available to order |
| EMMA ID | EM:04462 |
| International strain name | B6;129P2-Prmt2tm1Yah/Orl |
| Alternative name | Prmt2<3HP> |
| Strain type | Targeted Mutant Strains : Other targeted |
| Allele/Transgene symbol | Prmt2tm1Yah |
| Gene/Transgene symbol | Prmt2 |
Information from provider
| Provider | Yann Herault |
| Provider affiliation | CNRS IEM UMR 6218 |
| Genetic information | Insertion by homologous recombination of targeting vector containing loxP site in the locus of Prmt2 (Hrmt1l1) gene (MMU10). |
| Phenotypic information | Strain containing a loxP site on the Prmt2 (Hrmt1l1) gene. |
| Breeding history | maintained on C57BL/6 background |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Literature references
- Modeling the monosomy for the telomeric part of human chromosome 21 reveals haploinsufficient genes modulating the inflammatory and airway responses.;Besson Vanessa, Brault Véronique, Duchon Arnaud, Togbe Dieudonné, Bizot Jean-Charles, Quesniaux Valérie F J, Ryffel Bernard, Hérault Yann, ;2007;Human molecular genetics;16;2040-52; 17591625