Symbol Name ID |
Kmt2a
lysine (K)-specific methyltransferase 2A MGI:96995 |
Darker colors indicate more annotations |
Human Phenotypes | Purpura |
Myelofibrosis |
Hemophagocytosis |
Acute myeloid leukemia |
Myeloproliferative disorder |
Extramedullary hematopoiesis |
Lymphoma |
Splenomegaly |
Disease(s) Associated with KMT2A | ||||||||
acute myeloid leukemia | ||||||||
myelofibrosis | ||||||||
non-Hodgkin lymphoma |
Mouse Phenotypes | abnormal hematopoietic system morphology/development |
abnormal blood cell morphology/development |
abnormal definitive hematopoiesis |
abnormal common myeloid progenitor cell morphology |
decreased common myeloid progenitor cell number |
abnormal myelopoiesis |
anemia |
decreased bone marrow cell number |
abnormal common lymphocyte progenitor cell morphology |
decreased erythroid progenitor cell number |
increased erythroid progenitor cell number |
abnormal proerythroblast morphology |
decreased erythrocyte cell number |
decreased hemoglobin content |
thrombocytopenia |
decreased B cell number |
decreased pre-B cell number |
decreased hematopoietic stem cell number |
abnormal hematopoietic stem cell morphology |
abnormal bone marrow cell physiology |
abnormal hematopoietic stem cell physiology |
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Availability | Mouse Genotype | |||||||||||||||||||||
Kmt2atm1.1Brad/Kmt2atm1.1Brad | ||||||||||||||||||||||
Kmt2atm1.1Mlc/Kmt2atm1.1Mlc | ||||||||||||||||||||||
Kmt2atm2.1Mlc/Kmt2atm2.1Mlc | ||||||||||||||||||||||
Kmt2atm1Clgr/Kmt2a+ | ||||||||||||||||||||||
Kmt2atm1Sjk/Kmt2a+ | ||||||||||||||||||||||
Kmt2atm1.1Erns/Kmt2atm1.1Erns Tg(Mx1-cre)1Cgn/0 (conditional) |
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Kmt2atm1.1Erns/Kmt2atm1.1Erns (conditional) | ||||||||||||||||||||||
Kmt2atm1Brad/Kmt2atm1Brad Commd10Tg(Vav1-icre)A2Kio/? (conditional) |
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 05/28/2024 MGI 6.13 |
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