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Symbol Name ID |
Epb42
erythrocyte membrane protein band 4.2 MGI:95402 |
| Darker colors indicate more annotations |
| Human Phenotypes | Increased mean corpuscular hemoglobin concentration |
Reticulocytosis |
Anemia |
Hemolytic anemia |
Spontaneous hemolytic crises |
Spherocytosis |
Increased red cell osmotic fragility |
Abnormal leukocyte count |
Hypofibrinogenemia |
Hypercoagulability |
Abnormal platelet count |
Extramedullary hematopoiesis |
Splenomegaly |
| Disease(s) Associated with EPB42 | |||||||||||||
| hereditary spherocytosis | |||||||||||||
| hereditary spherocytosis type 5 |
| Mouse Phenotypes | increased spleen weight |
anemia |
abnormal erythrocyte morphology |
decreased erythrocyte cell number |
decreased hematocrit |
decreased hemoglobin content |
increased mean corpuscular hemoglobin concentration |
decreased mean corpuscular volume |
spherocytosis |
reticulocytosis |
increased spleen iron level |
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| Availability | Mouse Genotype | |||||||||||
| Epb42tm1Llp/Epb42tm1Llp | ||||||||||||
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 04/23/2024 MGI 6.23 |
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