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Symbol Name ID |
Epor
erythropoietin receptor MGI:95408 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral hemorrhage |
Pericarditis |
Hypertension |
Raynaud phenomenon |
Myocardial infarction |
Lymphadenopathy |
Splenomegaly |
| Disease(s) Associated with EPOR | |||||||
| familial erythrocytosis 1 | |||||||
| systemic lupus erythematosus |
| Mouse Phenotypes | abnormal blood vessel morphology |
abnormal lung vasculature morphology |
abnormal physiological neovascularization |
decreased angiogenesis |
abnormal vascular endothelial cell migration |
heart right ventricle hypertrophy |
abnormal heart development |
abnormal heart morphology |
abnormal interventricular septum morphology |
ventricular hypoplasia |
thick ventricular wall |
abnormal interventricular groove morphology |
pericardial edema |
detached epicardium |
abnormal heart right ventricle pressure |
abnormal myocardial fiber physiology |
pulmonary hypertension |
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| Availability | Mouse Genotype | |||||||||||||||||
| Eportm1Jae/Eportm1Jae | ||||||||||||||||||
| Eportm1Lizon/Eportm1Lizon Tg(Gata1-Epor)AMym/0 |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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