Symbol Name ID |
Kmt2a
lysine (K)-specific methyltransferase 2A MGI:96995 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hemophagocytosis |
Acute myeloid leukemia |
Myeloproliferative disorder |
Splenomegaly |
Disease(s) Associated with KMT2A | ||||
acute myeloid leukemia | ||||
myelofibrosis |
Mouse Phenotypes | immune system phenotype |
abnormal myelopoiesis |
decreased B cell number |
decreased pre-B cell number |
|
Availability | Mouse Genotype | ||||
Kmt2atm1Clgr/Kmt2a+ | |||||
Kmt2atm1Sjk/Kmt2a+ | |||||
Cd19tm1(cre)Cgn/Cd19+ Kmt2atm1.1Erns/Kmt2atm1.1Erns (conditional) |
* | ||||
Kmt2atm1.1Erns/Kmt2atm1.1Erns Tg(Lck-cre)1Cwi/0 (conditional) |
* | ||||
Kmt2atm1.1Erns/Kmt2atm1.1Erns Lyz2tm1(cre)Ifo/Lyz2+ (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 04/23/2024 MGI 6.23 |
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