PRDM12

Information PRDM12

Description

This gene encodes a transcriptional regulator of sensory neuronal specification that plays a critical role in pain perception. The encoded protein contains an N-terminal PRDI-BF1 and RIZ homology (PR) domain, a SET domain, and three C-terminal C2H2 zinc finger DNA-binding domains. Naturally occurring mutations in this gene are associated with congenital insensitivity to pain (CIP), and hereditary sensory and autonomic neuropathies (HSAN's) affecting peripheral sensory and autonomic neurons. Deregulation of this gene is associated with solid cancers and hematological malignancies including chronic myeloid leukaemia. [provided by RefSeq, Mar 2017]

Full Name

PR/SET domain 12

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
5,812
Non-redundant peaks
5,812

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000130711
UniProt
Q9H4Q4
Genevisible
Q9H4Q4
RefSeq
NM_021619
Aliases
PFM9
All peaks PRDM12
Download BED file
Non redundant peaks PRDM12
Download BED file
SEQUENCES PRDM12
Download FASTA file
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Datasets Table for PRDM12

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
PRDM12 HEK293 ENCODE Homo sapiens ENCSR760AAY 5,812
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.