CHD8

Information CHD8

Description

This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]

Full Name

chromodomain helicase DNA binding protein 8

Source NCBI

Species

Homo sapiens [tax_id: 9606]

Genome

hg38

ReMap Statistics

Datasets
5
Biotypes
1
Peaks
68,381
Non-redundant peaks
59,663

TF Classification

Super Class
NA
Class
NA
Familly
NA
Sub Familly
NA

Source TFClass

External IDs

NCBI Gene
57680
Official Gene Name
CHD8
JASPAR
Ensembl
ENSG00000100888
UniProt
Q9HCK8
Genevisible
Q9HCK8
RefSeq
NM_001170629
Aliases
DUPLIN; KIAA1564
All peaks CHD8
Download BED file
Non redundant peaks CHD8
Download BED file
SEQUENCES CHD8
Download FASTA file
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Datasets Table for CHD8

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
CHD8 T-47D ETOH_45 GEO Homo sapiens GSE62428 22,957
CHD8 T-47D R5020_45 GEO Homo sapiens GSE62428 8,271
CHD8 T-47D GEO Homo sapiens GSE62428 22,463
CHD8 T-47D R5020_5 GEO Homo sapiens GSE62428 2,809
CHD8 T-47D ETOH_5 GEO Homo sapiens GSE62428 11,881
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks