PML

Information PML

Description

The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This phosphoprotein localizes to nuclear bodies where it functions as a transcription factor and tumor suppressor. Its expression is cell-cycle related and it regulates the p53 response to oncogenic signals. The gene is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL). Extensive alternative splicing of this gene results in several variations of the protein's central and C-terminal regions; all variants encode the same N-terminus. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

Full Name

promyelocytic leukemia

Source NCBI

ReMap Statistics

Datasets
3
Biotypes
3
Peaks
77,076
Non-redundant peaks
62,747

TF Classification

Super Class
Unknown
Class
Unknown
Familly
Unknown
Sub Familly
Unknown

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000140464
UniProt
P29590
Genevisible
P29590
RefSeq
NM_002675
Aliases
MYL; PP8675; RNF71; TRIM19
All peaks PML
Download BED file
Non redundant peaks PML
Download BED file
SEQUENCES PML
Download FASTA file
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Datasets Table for PML

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
PML GM12878 ENCODE Homo sapiens ENCSR000BQM 21,871
PML K-562 ENCODE Homo sapiens ENCSR000BQY 41,628
PML MCF-7 ENCODE Homo sapiens ENCSR000BUZ 13,577
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.