SP2

Information SP2

Description

This gene encodes a member of the Sp subfamily of Sp/XKLF transcription factors. Sp family proteins are sequence-specific DNA-binding proteins characterized by an amino-terminal trans-activation domain and three carboxy-terminal zinc finger motifs. This protein contains the least conserved DNA-binding domain within the Sp subfamily of proteins, and its DNA sequence specificity differs from the other Sp proteins. It localizes primarily within subnuclear foci associated with the nuclear matrix, and can activate or in some cases repress expression from different promoters. [provided by RefSeq, Jul 2008]

Full Name

Sp2 transcription factor

Source NCBI

ReMap Statistics

Datasets
6
Biotypes
5
Peaks
86,048
Non-redundant peaks
49,191

TF Classification

Super Class
Zinc-coordinating DNA-binding domains
Class
C2H2 zinc finger factors
Familly
Three-zinc finger Krüppel-related factors
Sub Familly
Sp1-like factors

Source TFClass

External IDs

JASPAR
MA0516
Ensembl
ENSG00000167182
UniProt
Q02086
Genevisible
Q02086
RefSeq
NM_003110
Aliases
KIAA0048
All peaks SP2
Download BED file
Non redundant peaks SP2
Download BED file
SEQUENCES SP2
Download FASTA file
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Datasets Table for SP2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
SP2 HEK293 ENCODE Homo sapiens ENCSR807LQP 31,764
SP2 HEK293T ENA Homo sapiens ERP007114 10,808
SP2 Hep-G2 ENCODE Homo sapiens ENCSR000BOU 1,034
SP2 K-562 ENCODE Homo sapiens ENCSR000BNL 5,297
SP2 WA01 ENCODE Homo sapiens ENCSR000BQG 2,252
SP2 HEK293 GEO Homo sapiens GSE76494 34,893
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.