GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000044
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
GO_REF:0000052
Gene Ontology annotation based on curation of immunofluorescence data
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000117
Electronic Gene Ontology annotations created by ARBA machine learning models
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:15300250
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
PMID:16155193
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
PMID:17299439
CHARGE syndrome: an update.
PMID:17684005
Immunological abnormalities in CHARGE syndrome.
PMID:17937444
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype.
PMID:20130577
CHD7 cooperates with PBAF to control multipotent neural crest formation.
PMID:20453063
CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome.
PMID:28533432
The ATP-dependent chromatin remodeling enzymes CHD6, CHD7, and CHD8 exhibit distinct nucleosome binding and remodeling activities.
PMID:9556299
CHARGE syndrome: report of 47 cases and review.
Reactome:R-HSA-9944087
CHD6-9-dependent ATP hydrolysis
Reactome:R-HSA-9944450
CHD7 and CHD8 bind FAM124B
PMID:23134727
Chromatin remodeling by the CHD7 protein is impaired by mutations that cause human developmental disorders.
PMID:22646239
Identification of CHD7S as a novel splicing variant of CHD7 with functions similar and antagonistic to those of the full-length CHD7L.
PMID:19251738
Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns.
PMID:20657823
CHD7 targets active gene enhancer elements to modulate ES cell-specific gene expression.
PMID:23319608
Brg1 governs distinct pathways to direct multiple aspects of mammalian neural crest cell development.
PMID:26102480
A critical role for the chromatin remodeller CHD7 in anterior mesoderm during cardiovascular development.
PMID:29440260
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors.
PMID:23285124
Identification and characterization of FAM124B as a novel component of a CHD7 and CHD8 containing complex.
PMID:20591827
CHD7 functions in the nucleolus as a positive regulator of ribosomal RNA biogenesis.
file:human/CHD7/CHD7-source-evidence.json
CHD7 authenticated source facts and evidence-access ledger