(Q5011082)

BRK domain superfamily

1 reference

P-loop containing nucleoside triphosphate hydrolase

1 reference

SNF2-like, N-terminal domain superfamily

1 reference

Helicase superfamily 1/2, ATP-binding domain, protein family

1 reference

Chromo domain, protein family

1 reference

Helicase, C-terminal domain, protein family

1 reference

BRK domain, protein family

1 reference

1 reference

Chromo/chromo shadow domain, protein family

1 reference

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

13 November 2019

1 reference

13 November 2019

1 reference

8 April 2019

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

CHARGE syndrome: an update

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

RNA polymerase II cis-regulatory region sequence-specific DNA binding

TAS

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

hydrolase activity, acting on acid anhydrides

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

3 references

8 April 2019

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

8 April 2019

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome

IntAct protein interaction database

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

8 April 2019

CHD7 cooperates with PBAF to control multipotent neural crest formation

IntAct protein interaction database

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

2 references

promoter-specific chromatin binding

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

4 references

8 April 2019

CHARGE syndrome: an update

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

8 April 2019

CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

skeletal system development

IDA

biological process

1 reference

8 April 2019

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

semicircular canal morphogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

adult heart development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

cranial nerve development

1 reference

8 April 2019

CHARGE syndrome: report of 47 cases and review

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

olfactory nerve development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

sensory perception of sound

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

transcription, DNA-templated

1 reference

21 June 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P2D1&geneProductId=UniProtKB:Q9P2D1

epithelium development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

genitalia development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

regulation of growth hormone secretion

1 reference

8 April 2019

CHARGE syndrome: report of 47 cases and review

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

central nervous system development

1 reference

8 April 2019

CHARGE syndrome: report of 47 cases and review

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

Immunological abnormalities in CHARGE syndrome

T cell differentiation

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

blood vessel development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

retina development in camera-type eye

1 reference

8 April 2019

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

positive regulation of multicellular organism growth

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

camera-type eye development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

olfactory bulb development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

female genitalia development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

regulation of neurogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

adult walking behavior

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

embryonic hindlimb morphogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

ventricular trabecula myocardium morphogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

positive regulation of transcription by RNA polymerase II

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

right ventricular compact myocardium morphogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

atrioventricular canal development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

blood vessel remodeling

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

cardiac septum morphogenesis

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

chromatin organization

1 reference

8 April 2019

roof of mouth development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

secondary palate development

1 reference

8 April 2019

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

response to bacterium

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

regulation of transcription, DNA-templated

1 reference

8 April 2019

Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2D1

http://purl.uniprot.org/uniprot/Q9P2D1

NAS

exact match

1 reference

1 reference

Helicase, C-terminal

1 reference

Chromo/chromo shadow domain

1 reference

SNF2-related, N-terminal domain

1 reference

BRK domain

1 reference

Helicase superfamily 1/2, ATP-binding domain

1 reference