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Symbol Name ID |
Kcne2
potassium voltage-gated channel, Isk-related subfamily, gene 2 MGI:1891123 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Thromboembolism |
Thromboembolic stroke |
| Disease(s) Associated with KCNE2 | ||
| familial atrial fibrillation |
| Mouse Phenotypes | hematopoietic system phenotype |
anemia |
hypochromic microcytic anemia |
decreased erythrocyte cell number |
decreased hematocrit |
decreased hemoglobin content |
decreased mean corpuscular hemoglobin |
decreased mean corpuscular volume |
increased red blood cell distribution width |
thrombocytosis |
decreased spleen iron level |
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| Availability | Mouse Genotype | |||||||||||
| Kcne2tm1a(EUCOMM)Wtsi/Kcne2tm1a(EUCOMM)Wtsi | * | |||||||||||
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 05/21/2024 MGI 6.23 |
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