CHD7
Information CHD7
- Description
This gene encodes a protein containing two chromodomains and an ATP-binding helicase domain that functions as a regulator of transcription. Mutations in this gene result in an array of development defects, including inner ear problems. Mice defective for this gene exhibit many of the clinical features of the CHARGE syndrome caused by mutations in the homologous gene in human. [provided by RefSeq, Sep 2015]
- Full Name
chromodomain helicase DNA binding protein 7
Source UniprotKB
- Species
Mus musculus [tax_id: 10090]
- Genome
mm10
ReMap Statistics
- Datasets
- 6
- Biotypes
- 3
- Peaks
- 14,517
- Non-redundant peaks
- 11,648
TF Classification
- Familly
- NA
- Sub Familly
- NA
Source JASPAR
External IDs
- NCBI Gene
- 320790
- Official Gene Name
- Chd7
- JASPAR
- MGI
- MGI:2444748
- Ensembl
- ENSMUSG00000041235
- UniProt
- A2AJK6
- Genevisible
- A2AJK6
- RefSeq
- NM_001355382
- Aliases
- A730019I05Rik; Cycn; Cyn; Dz; Edy; Flo; GENA 47; GENA 60; Gena 52; Lda; Mt; Obt; Todo; WBE1; Whi
Datasets Table for CHD7
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| CHD7 | 416B | CBFB-MYH11 | GEO | Mus musculus | GSE83956 | 1,198 | ||
| CHD7 | 416B | CBFB-MYH11_Dox | GEO | Mus musculus | GSE83956 | 1,380 | ||
| CHD7 | 416B | GEO | Mus musculus | GSE83956 | 988 | |||
| CHD7 | cerebellum | GEO | Mus musculus | GSE93719 | 994 | |||
| CHD7 | mESC | GEO | Mus musculus | GSE22341 | 8,906 | |||
| CHD7 | 416B | Dox | GEO | Mus musculus | GSE83956 | 1,051 | ||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |