Symbol Name ID |
Epor
erythropoietin receptor MGI:95408 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal bleeding |
Epistaxis |
Cerebral hemorrhage |
Increased hematocrit |
Abnormal hemoglobin |
Increased circulating hemoglobin concentration |
Hemolytic anemia |
Polycythemia |
Increased red blood cell mass |
Leukopenia |
Peripheral thrombosis |
Thromboembolism |
Venous thrombosis |
Thrombocytopenia |
Splenomegaly |
Disease(s) Associated with EPOR | |||||||||||||||
familial erythrocytosis 1 | |||||||||||||||
systemic lupus erythematosus |
Mouse Phenotypes | hematopoietic system phenotype |
abnormal definitive hematopoiesis |
abnormal erythropoiesis |
anemia |
impaired hematopoiesis |
absent erythroid progenitor cell |
increased erythroid progenitor cell number |
abnormal erythrocyte morphology |
decreased erythrocyte cell number |
decreased hematocrit |
increased hematocrit |
abnormal embryonic erythrocyte morphology |
|
Availability | Mouse Genotype | ||||||||||||
Eportm1Cos/Eportm1Cos | |||||||||||||
Eportm1Jae/Eportm1Jae | |||||||||||||
Eportm1Jni/Eportm1Jni | |||||||||||||
Eportm1Lizon/Eportm1Lizon | * | ||||||||||||
Eportm2Jni/Eportm2Jni | |||||||||||||
Hprt1tm1(ACTB-Epor)Unc/Hprt1tm1(ACTB-Epor)Unc | * | ||||||||||||
Hprt1tm1(ACTB-Epor)Unc/Y | * |
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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