MORC2

Information MORC2

Description

This gene encodes a member of the Microrchidia (MORC) protein superfamily. The encoded protein is known to regulate the condensation of heterochromatin in response to DNA damage and play a role in repressing transcription. The protein has been found to regulate the activity of ATP citrate lyase via specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also plays a role in lipogenesis and adipocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016]

Full Name

MORC family CW-type zinc finger 2

Source NCBI

ReMap Statistics

Datasets
7
Biotypes
3
Peaks
52,491
Non-redundant peaks
41,943

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000133422
UniProt
Q9Y6X9
Genevisible
Q9Y6X9
RefSeq
NM_001303256
Aliases
AC004542.C22.1; CMT2Z; KIAA0852; ZCW3; ZCWCC1
All peaks MORC2
Download BED file
Non redundant peaks MORC2
Download BED file
SEQUENCES MORC2
Download FASTA file
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Datasets Table for MORC2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
MORC2 HeLa V5-HUSH-KO GEO Homo sapiens GSE95451 15,627
MORC2 HeLa V5-MORC2-KO GEO Homo sapiens GSE95451 5,679
MORC2 HeLa V5-MORC2-KO-W505A-MORC2-mut GEO Homo sapiens GSE95451 12,462
MORC2 H9 GEO Homo sapiens GSE95374 16,584
MORC2 K-562 GEO Homo sapiens GSE95374 1,828
MORC2 K-562 MPP8-KO GEO Homo sapiens GSE95374 135
MORC2 K-562 TASOR-KO GEO Homo sapiens GSE95374 176
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.