- increased exploration in new environment / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased hemoglobin content / IMPC
- decreased mean corpuscular hemoglobin concentration / IMPC
- decreased mean corpuscular volume / IMPC
- decreased circulating cholesterol level / IMPC
- abnormal skin condition / IMPC
- decreased circulating free fatty acids level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- decreased circulating HDL cholesterol level / IMPC
B6;129P2-Rhdtm1Goo/Orl
| Status | Available to order |
| EMMA ID | EM:11706 |
| Citation information | RRID:IMSR_EM:11706 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-Rhdtm1Goo/Orl |
| Alternative name | GOO1 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Rhdtm1Goo |
| Gene/Transgene symbol | Rhd |
Information from provider
| Provider | Dominique GOOSSENS |
| Provider affiliation | UMR_S1134-Inserm - Dept de recherches biologiques sur le globule rouge, Institut National de la Transfusion Sanguine-Inserm |
| Genetic information | Rhd (erythroid membrane protein) gene knock-out. |
| Phenotypic information | Homozygous:No clinical or cellular abnormalities, complete loss of erythrocyte membrane expression of Rhd, and of Icam4 (with consequent decreased adhesion to endothelial cell line)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
- 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
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