Homo sapiens Protein: CHD8 | |||||||||||||||||||||||||||
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Summary | |||||||||||||||||||||||||||
InnateDB Protein | IDBP-361108.5 | ||||||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||||||
Gene Symbol | CHD8 | ||||||||||||||||||||||||||
Protein Name | chromodomain helicase DNA binding protein 8 | ||||||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||||||
Ensembl Protein | ENSP00000406288 | ||||||||||||||||||||||||||
InnateDB Gene | IDBG-2645 (CHD8) | ||||||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||||||
Function | DNA helicase that acts as a chromatin remodeling factor and regulates transcription. Acts as a transcription repressor by remodeling chromatin structure and recruiting histone H1 to target genes. Suppresses p53/TP53-mediated apoptosis by recruiting histone H1 and preventing p53/TP53 transactivation activity. Acts as a negative regulator of Wnt signaling pathway by regulating beta-catenin (CTNNB1) activity. Negatively regulates CTNNB1- targeted gene expression by being recruited specifically to the promoter regions of several CTNNB1 responsive genes. Involved in both enhancer blocking and epigenetic remodeling at chromatin boundary via its interaction with CTCF. Acts as a suppressor of STAT3 activity by suppressing the LIF-induced STAT3 transcriptional activity. Also acts as a transcription activator via its interaction with ZNF143 by participating in efficient U6 RNA polymerase III transcription. {ECO:0000269PubMed:17938208, ECO:0000269PubMed:18378692}. | ||||||||||||||||||||||||||
Subcellular Localization | Nucleus {ECO:0000269PubMed:18378692, ECO:0000269PubMed:20453063}. Note=Localizes to the promoter regions of several CTNNB1-responsive genes. Also present at known CTCF target sites. | ||||||||||||||||||||||||||
Disease Associations | Autism 18 (AUTS18) [MIM:615032]: A complex multifactorial, pervasive developmental disorder characterized by impairments in reciprocal social interaction and communication, restricted and stereotyped patterns of interests and activities, and the presence of developmental abnormalities by 3 years of age. Most individuals with autism also manifest moderate mental retardation. {ECO:0000269PubMed:23160955}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. | ||||||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||||||
Comments | |||||||||||||||||||||||||||
Interactions | |||||||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 39 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||||||
InterPro |
IPR000330
SNF2-related IPR000953 Chromo domain/shadow IPR001650 Helicase, C-terminal IPR006576 BRK domain IPR006935 Helicase/UvrB domain IPR011545 DEAD/DEAH box helicase domain IPR014001 Helicase, superfamily 1/2, ATP-binding domain IPR016197 Chromo domain-like IPR023780 Chromo domain IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00176
PF00271 PF07533 PF04851 PF00270 PF00385 |
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PRINTS | |||||||||||||||||||||||||||
PIRSF | |||||||||||||||||||||||||||
SMART |
SM00298
SM00490 SM00592 SM00487 |
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TIGRFAMs | |||||||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||||||
Modification | |||||||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||||||
SwissProt | Q9HCK8 | ||||||||||||||||||||||||||
PhosphoSite | PhosphoSite-Q9HCK8 | ||||||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||||||
Entrez Gene | 57680 | ||||||||||||||||||||||||||
UniGene | Hs.718220 | ||||||||||||||||||||||||||
RefSeq | NP_065971 | ||||||||||||||||||||||||||
HUGO | HGNC:20153 | ||||||||||||||||||||||||||
OMIM | 610528 | ||||||||||||||||||||||||||
CCDS | CCDS45081 | ||||||||||||||||||||||||||
HPRD | 16712 | ||||||||||||||||||||||||||
IMGT | |||||||||||||||||||||||||||
EMBL | AB046784 AK131077 AL135744 AL161747 AL834524 BC011695 BC025964 BC036920 BC063693 BC073903 BC098452 CB043942 CR749315 | ||||||||||||||||||||||||||
GenPept | AAH11695 AAH25964 AAH36920 AAH63693 AAH73903 AAH98452 BAB13390 BAC85127 CAD39180 CAH18170 | ||||||||||||||||||||||||||