# Chromodomain helicase DNA binding protein 7

> mammalian protein found in Homo sapiens

**Wikidata**: [Q5011082](https://www.wikidata.org/wiki/Q5011082)  
**Source**: https://4ort.xyz/entity/chromodomain-helicase-dna-binding-protein-7-q5011082


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9P2D1)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
5. [CHARGE syndrome: an update](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
6. [CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
7. [CHD7 cooperates with PBAF to control multipotent neural crest formation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
8. [CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
9. [Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P2D1&geneProductId=UniProtKB:Q9P2D1)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P2D1&geneProductId=UniProtKB:Q9P2D1)
11. [CHARGE syndrome: report of 47 cases and review](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
12. [Mutations in a new member of the chromodomain gene family cause CHARGE syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
13. [Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
14. [Immunological abnormalities in CHARGE syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1)
15. Ensembl Release 99
16. Identifiers.org