ZMYM3

Information ZMYM3

Description

This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010]

Full Name

zinc finger MYM-type containing 3

Source NCBI

ReMap Statistics

Datasets
8
Biotypes
4
Peaks
173,522
Non-redundant peaks
86,464

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000147130
UniProt
Q14202
Genevisible
Q14202
RefSeq
NM_001171162
Aliases
DXS6673E; KIAA0385; MYM; XFIM; ZNF198L2; ZNF261
All peaks ZMYM3
Download BED file
Non redundant peaks ZMYM3
Download BED file
SEQUENCES ZMYM3
Download FASTA file
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Datasets Table for ZMYM3

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ZMYM3 Hep-G2 ENCODE Homo sapiens ENCSR848YWD 20,738
ZMYM3 K-562 ENCODE Homo sapiens ENCSR102KIN 58,126
ZMYM3 GM12878 GEO Homo sapiens GSE97661 15,398
ZMYM3 Hep-G2 Ab_JH39-2-2F10 GEO Homo sapiens GSE97661 24,921
ZMYM3 Hep-G2 AC_JH39-2-2B9 GEO Homo sapiens GSE97661 14,974
ZMYM3 Hep-G2 AC_R259-2-2C3 GEO Homo sapiens GSE97661 896
ZMYM3 K-562 Ab_JH39-2-2F10 GEO Homo sapiens GSE97661 36,915
ZMYM3 MCF-7 GEO Homo sapiens GSE97661 1,554
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.

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

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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.