ZNF81

Information ZNF81

Description

This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017]

Full Name

zinc finger protein 81

Source NCBI

ReMap Statistics

Datasets
1
Biotypes
1
Peaks
197
Non-redundant peaks
197

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000197779
UniProt
P51508
Genevisible
P51508
RefSeq
NM_007137
Aliases
HFZ20
All peaks ZNF81
Download BED file
Non redundant peaks ZNF81
Download BED file
SEQUENCES ZNF81
Download FASTA file
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Datasets Table for ZNF81

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
ZNF81 HEK293T GEO Homo sapiens GSE78099 197
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.