CHD7
Information CHD7
- Description
This gene encodes a protein that contains several helicase family domains. Mutations in this gene have been found in some patients with the CHARGE syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
- Full Name
chromodomain helicase DNA binding protein 7
- Source NCBI
ReMap Statistics
- Datasets
- 7
- Biotypes
- 3
- Peaks
- 218,533
- Non-redundant peaks
- 173,031
TF Classification
- Super Class
- Unknown
- Class
- Unknown
- Familly
- Unknown
- Sub Familly
- Unknown
Source TFClass
External IDs
- JASPAR
- Ensembl
- ENSG00000171316
- UniProt
- Q9P2D1
- Genevisible
- Q9P2D1
- RefSeq
- NM_001316690
- Aliases
- FLJ20357; FLJ20361; KIAA1416
Datasets Table for CHD7
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| CHD7 | K-562 | ENCODE | Homo sapiens | ENCSR000AVD | 2,492 | |||
| CHD7 | WA01 | ENCODE | Homo sapiens | ENCSR000AVA | 16,734 | |||
| CHD7 | hiPSC | GEO | Homo sapiens | GSE108506 | 100,805 | |||
| CHD7 | hiPSC | AF22_abD3F5 | GEO | Homo sapiens | GSE108506 | 7,307 | ||
| CHD7 | hiPSC | derived_lt-NES | GEO | Homo sapiens | GSE108506 | 62,308 | ||
| CHD7 | hiPSC | derived_lt-NES_AF22 | GEO | Homo sapiens | GSE108506 | 259 | ||
| CHD7 | hiPSC | derived_neural-crest-cell | GEO | Homo sapiens | GSE108506 | 28,628 | ||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |