- abnormal thymus morphology / IMPC
- increased circulating cholesterol level / IMPC
- enlarged lymph nodes / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- abnormal lymph node morphology / IMPC
- small testis / IMPC
- abnormal testis morphology / IMPC
- increased circulating total protein level / IMPC
- increased circulating HDL cholesterol level / IMPC
- enlarged heart / IMPC
- abnormal heart morphology / IMPC
- enlarged thymus / IMPC
B6;129P2-Rhagtm1Goo/Orl
| Status | Available to order |
| EMMA ID | EM:11707 |
| Citation information | RRID:IMSR_EM:11707 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 | B6;129P2-Rhagtm1Goo/Orl |
| Alternative name | GOO2 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Rhagtm1Goo |
| Gene/Transgene symbol | Rhag |
Information from provider
| Provider | Dominique GOOSSENS |
| Provider affiliation | UMRS_1134 Inserm- Dept de recherches biologiques sur le globule rouge, Institut National de la Transfusion Sanguine-Inserm |
| Genetic information | Rhag erythroid membrane protein gene knock-out. |
| Phenotypic information | Homozygous:No clinical abnormalities; loss of Rhag erythrocyte membrane protein expression as well as of associated mouse Rh complex proteins; disruption of erythrocyte ammonium transport.Heterozygous:Normal |
| Breeding history | 129P2/OlaHsd x C57BL/6 background. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | no |
Information from EMMA
| Archiving centre | CNRS-TAAM – Typing and Archiving of Animal Models, Orléans, France |
| Animals used for archiving | heterozygous 129P2/OlaHsd x C57BL/6 males, wild-type C57BL/6 females |
| Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Overhydrated hereditary stomatocytosis / Orphanet_3203
- Rh deficiency syndrome / Orphanet_71275
IMPC phenotypes (gene matching)
Literature references
- Generation and characterisation of Rhd and Rhag null mice.;Goossens Dominique, Trinh-Trang-Tan Marie-Marcelle, Debbia Martine, Ripoche Pierre, Vilela-Lamego Camilo, Louache Fawzia, Vainchenker William, Colin Yves, Cartron Jean-Pierre, ;2010;British journal of haematology;148;161-72; 19807729
- Generation of mice with inactivated Rh or Rhag genes.;Goossens D, Bony V, Gane P, Colin Y, Cartron J-P, ;2006;Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine;13;164-6; 16581281
- Role of RhAG and AQP1 in NH3 and CO2 gas transport in red cell ghosts: a stopped-flow analysis.;Ripoche P, Goossens D, Devuyst O, Gane P, Colin Y, Verkman A S, Cartron J-P, ;2006;Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine;13;117-22; 16574458
- Maximal Oxygen Consumption Is Reduced in Aquaporin-1 Knockout Mice.;Al-Samir Samer, Goossens Dominique, Cartron Jean-Pierre, Nielsen Søren, Scherbarth Frank, Steinlechner Stephan, Gros Gerolf, Endeward Volker, ;2016;Frontiers in physiology;7;347; 27559317
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