ADNP

Information ADNP

Description

Vasoactive intestinal peptide is a neuroprotective factor that has a stimulatory effect on the growth of some tumor cells and an inhibitory effect on others. This gene encodes a protein that is upregulated by vasoactive intestinal peptide and may be involved in its stimulatory effect on certain tumor cells. The encoded protein contains one homeobox and nine zinc finger domains, suggesting that it functions as a transcription factor. This gene is also upregulated in normal proliferative tissues. Finally, the encoded protein may increase the viability of certain cell types through modulation of p53 activity. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]

Full Name

activity dependent neuroprotector homeobox

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
7,766
Non-redundant peaks
7,766

TF Classification

Super Class
Zinc-coordinating DNA-binding domains, Helix-turn-helix domains
Class
C2H2 zinc finger factors, Homeo domain factors
Familly
Factors with multiple dispersed zinc fingers, HD-ZF factors
Sub Familly
unclassified, ADNP

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000101126
UniProt
Q9H2P0
Genevisible
Q9H2P0
RefSeq
NM_001282531
Aliases
ADNP1; HVDAS; KIAA0784; MRD28
All peaks ADNP
Download BED file
Non redundant peaks ADNP
Download BED file
SEQUENCES ADNP
Download FASTA file
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Datasets Table for ADNP

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ADNP K-562 ENCODE Homo sapiens ENCSR440VKE 7,766
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.