- decreased hematocrit / MGI
- abnormal erythropoiesis / MGI
- abnormal heart development / MGI
- ventricular hypoplasia / MGI
- abnormal interventricular septum morphology / MGI
- abnormal liver morphology / MGI
- small liver / MGI
- pale liver / MGI
- abnormal liver physiology / MGI
- anemia / MGI
- abnormal blood vessel morphology / MGI
- abnormal placenta morphology / MGI
- edema / MGI
- pericardial edema / MGI
- no abnormal phenotype detected / MGI
- hyperoxia / MGI
- hyperventilation / MGI
- increased heart weight / MGI
- thick ventricular wall / MGI
- abnormal epicardium morphology / MGI
- increased erythroid progenitor cell number / MGI
- pallor / MGI
- increased hepatocyte apoptosis / MGI
- increased heart right ventricle weight / MGI
- increased left ventricle weight / MGI
- abnormal interventricular groove morphology / MGI
- abnormal myocardial fiber physiology / MGI
- enlarged myocardial fiber / MGI
- increased spleen weight / MGI
- hypoxia / MGI
- decreased oxygen consumption / MGI
- increased pulmonary ventilation / MGI
- decreased angiogenesis / MGI
- hemosiderosis / MGI
- mortality/aging / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- decreased fetal derived definitive erythrocyte cell number / MGI
STOCK EpoTg(TAg/Epo)134.3LCPjr/H
| Status | Available to order |
| EMMA ID | EM:02595 |
| Citation information | RRID:IMSR_EM:02595 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 | STOCK EpoTg(TAg/Epo)134.3LCPjr/H |
| Alternative name | Epo |
| Strain type | Transgenic Strains |
| Allele/Transgene symbol | EpoTg(TAg/Epo)134.3LCPjr |
| Gene/Transgene symbol | Epo |
Information from provider
| Provider | Patrick Maxwell |
| Provider affiliation | Wellcome Trust Centre for Human Genetics, University of Oxford |
| Genetic information | pBS construct with 16.5 kb of mouse Epo, including the entire Epo gene. A 2.7 kb Bgl1/BamH1 fragment of Sv40 DNA encoding "T" antigen was inserted into the 5'-UTR of the Epo gene. |
| Phenotypic information | The insertion of SV40 T antigen sequence in the 5'-UTR of the native Epo gene results in very little Epo production from the fusion gene. Homozygotes have incomplete Epo deficiency and are anaemic. The mice express SV40 T antigen in a regulated fashion (by anaemia and hypoxia) in Epo-producing cells. |
| Breeding history | Outcrossed to C57BL/6J. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | not known |
Information from EMMA
| Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal dominant secondary polycythemia / Orphanet_247511
MGI phenotypes (gene matching)
Literature references
- Identification of the renal erythropoietin-producing cells using transgenic mice.;Maxwell P H, Osmond M K, Pugh C W, Heryet A, Nicholls L G, Tan C C, Doe B G, Ferguson D J, Johnson M H, Ratcliffe P J, ;1993;Kidney international;44;1149-62; 8264149
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