KMT2B

Information KMT2B

Description

This gene encodes a protein which contains multiple domains including a CXXC zinc finger, three PHD zinc fingers, two FY-rich domains, and a SET (suppressor of variegation, enhancer of zeste, and trithorax) domain. The SET domain is a conserved C-terminal domain that characterizes proteins of the MLL (mixed-lineage leukemia) family. This gene is ubiquitously expressed in adult tissues. It is also amplified in solid tumor cell lines, and may be involved in human cancer. Two alternatively spliced transcript variants encoding distinct isoforms have been reported for this gene, however, the full length nature of the shorter transcript is not known. [provided by RefSeq, Jul 2008]

Full Name

lysine methyltransferase 2B

Source NCBI

ReMap Statistics

Datasets
3
Biotypes
2
Peaks
89,700
Non-redundant peaks
60,336

TF Classification

Super Class
Zinc-coordinating DNA-binding domains
Class
CXXC zinc finger factors
Familly
CpG-binding proteins
Sub Familly
None

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000272333
UniProt
Q9UMN6
Genevisible
Q9UMN6
RefSeq
NM_014727
Aliases
CXXC10; DYT28; HRX2; KIAA0304; MLL1B; MLL2; MLL4; TRX2; WBP-7; WBP7
All peaks KMT2B
Download BED file
Non redundant peaks KMT2B
Download BED file
SEQUENCES KMT2B
Download FASTA file
DOWNLOAD All ReMap
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Datasets Table for KMT2B

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
KMT2B AML GEO Homo sapiens GSE112074 32,673
KMT2B AML OG86 GEO Homo sapiens GSE112074 53,937
KMT2B B-cell GERMINAL_CENTER_TONSIL GEO Homo sapiens GSE67494 3,090
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.