CC2D1A

Information CC2D1A

Description

This gene encodes a transcriptional repressor that binds to a conserved 14-bp 5'-repressor element and regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA binding and transcriptional repressor activities of the protein are inhibited by calcium. A mutation in this gene results in a nonsyndromic form of cognitive disability (MRT3). [provided by RefSeq, Jul 2017]

Full Name

coiled-coil and C2 domain containing 1A

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
20,325
Non-redundant peaks
20,325

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000132024
UniProt
Q6P1N0
Genevisible
Q6P1N0
RefSeq
NM_017721
Aliases
FLJ20241; Freud-1; MRT3
All peaks CC2D1A
Download BED file
Non redundant peaks CC2D1A
Download BED file
SEQUENCES CC2D1A
Download FASTA file
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Datasets Table for CC2D1A

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
CC2D1A K-562 ENCODE Homo sapiens ENCSR343IFJ 20,325
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.