Symbol
| KMT2D
| contributors: mct/npt - updated : 28-04-2015
|
HGNC name
| lysine (K)-specific methyltransferase 2B
|
HGNC id
| 7133
|
corresponding disease(s)
|
KABUK1
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
tumoral
| somatic mutation
|  
|  
|  
|
in follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL) | |
Variant & Polymorphism
|
| |
Candidate gene
Marker
Therapy target
| | | |
| mice lacking mll2/kmt2b gene in adult forebrain excitatory neurons display impaired hippocampus-dependent memory function | |
mice heterozygous for two separate mutations in the SET domain of Mll2 or heterozygous Mll2 knockout mice were hyperglycaemic, hyperinsulinaemic and developed non-alcoholic fatty liver disease (PMIX: 23826075) |