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
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 6
- Biotypes
- 3
- Peaks
- 117,662
- Non-redundant peaks
- 99,005
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 55636
- Official Gene Name
- CHD7
- 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 | WA01 | ENCODE | Homo sapiens | ENCSR000AVA | 16,730 | |||
| CHD7 | K-562 | ENCODE | Homo sapiens | ENCSR000AVD | 2,484 | |||
| CHD7 | hiPSC | AF22_abD3F5 | GEO | Homo sapiens | GSE108506 | 7,307 | ||
| CHD7 | hiPSC | derived_lt-NES_AF22 | GEO | Homo sapiens | GSE108506 | 259 | ||
| CHD7 | hiPSC | derived_neural-crest-cell | GEO | Homo sapiens | GSE108506 | 28,628 | ||
| CHD7 | hiPSC | derived_lt-NES | GEO | Homo sapiens | GSE108506 | 62,254 | ||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |