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Gene : CHD8 Homo sapiens

Name  ? chromodomain helicase DNA binding protein 8 Cytological Location  14q11.2
Brief Description  chromodomain helicase DNA binding protein 8
Description  This gene encodes a member of the chromodomain-helicase-DNA binding protein family, which is characterized by a SNF2-like domain and two chromatin organization modifier domains. The encoded protein also contains brahma and kismet domains, which are common to the subfamily of chromodomain-helicase-DNA binding proteins to which this protein belongs. This gene has been shown to function in several processes that include transcriptional regulation, epigenetic remodeling, promotion of cell proliferation, and regulation of RNA synthesis. Allelic variants of this gene are associated with autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016]
  • synonyms:
  • HELSNF1,
  • DUPLIN,
  • OTTHUMG00000170759,
  • HELSNF1,
  • KIAA1564,
  • CHD8,
  • HGNC:20153,
  • AB046784,
  • uc001was.3,
  • AUTS18,
  • helicase with SNF2 domain 1,
  • NM_020920
  • identifiers:
  • 57680,
  • ENSG00000100888,
  • CHD8

Genome feature

Region: gene ? Length: 70925  
Location: 14:21385199-21456123 reverse strand Cyto location: 14q11.2


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Proteins

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SNPs

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Disease

1 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

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Expression

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Other

123 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

97 Rna Seq Results