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
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 |