CHD2
Information CHD2
- Description
The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
- Full Name
chromodomain helicase DNA binding protein 2
Source NCBI
- Species
Homo sapiens [tax_id: 9606]
- Genome
hg38
ReMap Statistics
- Datasets
- 7
- Biotypes
- 7
- Peaks
- 175,527
- Non-redundant peaks
- 109,908
TF Classification
- Super Class
- NA
- Class
- NA
- Familly
- NA
- Sub Familly
- NA
Source TFClass
External IDs
- NCBI Gene
- 1106
- Official Gene Name
- CHD2
- JASPAR
- Ensembl
- ENSG00000173575
- UniProt
- O14647
- Genevisible
- O14647
- RefSeq
- NM_001042572
- Aliases
- DKFZp547I1315; DKFZp686E01200; DKFZp781D1727; EEOC; FLJ38614
Datasets Table for CHD2
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |
|---|---|---|---|---|---|---|---|---|
| CHD2 | WA01 | ENCODE | Homo sapiens | ENCSR000EBT | 18,433 | |||
| CHD2 | SK-N-SH | ENCODE | Homo sapiens | ENCSR274SLQ | 57,140 | |||
| CHD2 | K-562 | ENCODE | Homo sapiens | ENCSR000EHD | 21,299 | |||
| CHD2 | Hep-G2 | ENCODE | Homo sapiens | ENCSR000EED | 17,669 | |||
| CHD2 | A-549 | ENCODE | Homo sapiens | ENCSR067HGI | 6,714 | |||
| CHD2 | GM12878 | ENCODE | Homo sapiens | ENCSR000DZR | 8,643 | |||
| CHD2 | HeLa-S3 | ENCODE | Homo sapiens | ENCSR000ECP | 45,629 | |||
| Target name | Target modification | Ecotype/Strain | Biotype | Biotype modification | Source | Species | Experiment | Peaks |