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Gene : CHD3 Homo sapiens

Name  ? chromodomain helicase DNA binding protein 3 Cytological Location  17p13.1
Brief Description  chromodomain helicase DNA binding protein 3
Description  This gene encodes a member of the CHD family of proteins which are characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. This protein is one of the components of a histone deacetylase complex referred to as the Mi-2/NuRD complex which participates in the remodeling of chromatin by deacetylating histones. Chromatin remodeling is essential for many processes including transcription. Autoantibodies against this protein are found in a subset of patients with dermatomyositis. Three alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
  • synonyms:
  • NM_001005273,
  • ZFH,
  • Mi2-ALPHA,
  • Mi-2a,
  • CHD3,
  • U08379,
  • ZFH,
  • HGNC:1918,
  • Mi2-ALPHA,
  • OTTHUMG00000150427,
  • uc002gjd.3,
  • Mi-2a
  • identifiers:
  • 1107,
  • ENSG00000170004,
  • CHD3

Genome feature

Region: gene ? Length: 27992  
Location: 17:7884764-7912755 Cyto location: 17p13.1

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



275 SNPs

5 Cross References

19 Data Sets

7 Homologues

2 Located Features

97 Rna Seq Results