CHD8 Chromosome 14

Chromodomain helicase DNA binding protein 8
270 variants 270 Health Risk

Upload your DNA to see your personal genotypes for variants in CHD8.

What This Gene Does
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]
Gene Info
Gene Group
"SNF2 related family|Small nucleolar RNA protein coding host genes"
Locus Type
gene with protein product
Location
14q11.2
Ensembl
ENSG00000100888
Associated Conditions (22)
Intellectual developmental disorder with autism and macrocephaly
Inborn genetic diseases
Autism spectrum disorder
CHD8-related disorder
Congenital ptosis
Overgrowth
Fatigable weakness
Increased muscle fatiguability
Macrocephaly
Complex neurodevelopmental disorder
See cases
Intellectual disability
Developmental disorder
Marfanoid habitus and intellectual disability
Neurodevelopmental disorder
CHD8-associated Neurodevelopmental syndrome
Rare genetic intellectual disability
Familial prostate cancer
Uterine corpus endometrial carcinoma
Glioma susceptibility 1
+2 more conditions
Key Variants
All Variants (270)
RSID Category Clinical Significance Conditions
RS778452195 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778530750 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS778904376 Health Risk Conflicting classifications of pathogenicity See cases, See cases
RS779470673 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS779756082 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS780618366 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS866434305 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS898418482 Health Risk Conflicting classifications of pathogenicity
RS906914158 Health Risk Conflicting classifications of pathogenicity Intellectual disability, Inborn genetic diseases, Intellectual disability
RS915195873 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS919583163 Health Risk Conflicting classifications of pathogenicity
RS1057523712 Health Risk Likely pathogenic
RS1064795655 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Autism spectrum disorder, CHD8-related disorder
RS1064796666 Health Risk Likely pathogenic
RS1373475251 Health Risk Likely pathogenic CHD8-related disorder, CHD8-related disorder
RS1394349467 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1555313219 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1555314174 Health Risk Likely pathogenic
RS1555314317 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1555314609 Health Risk Likely pathogenic Developmental disorder, Developmental disorder
RS1555315221 Health Risk Likely pathogenic
RS1555315488 Health Risk Likely pathogenic
RS1594329885 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1594331875 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1594340060 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1594344768 Health Risk Likely pathogenic Marfanoid habitus and intellectual disability, Marfanoid habitus and intellectual disability
RS1594349020 Health Risk Likely pathogenic
RS1887974151 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS1888355872 Health Risk Likely pathogenic
RS2139467378 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2139478439 Health Risk Likely pathogenic
RS2139478468 Health Risk Likely pathogenic
RS2139481823 Health Risk Likely pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2139484699 Health Risk Likely pathogenic Neurodevelopmental disorder, Neurodevelopmental disorder
RS2139499311 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2139499999 Health Risk Likely pathogenic CHD8-associated Neurodevelopmental syndrome, CHD8-associated Neurodevelopmental syndrome
RS2139531134 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501853049 Health Risk Likely pathogenic
RS2501857970 Health Risk Likely pathogenic Rare genetic intellectual disability, Rare genetic intellectual disability
RS2501858533 Health Risk Likely pathogenic
RS2501859189 Health Risk Likely pathogenic
RS2501886630 Health Risk Likely pathogenic
RS2501896438 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501897802 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501901102 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501923179 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2501925066 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501930345 Health Risk Likely pathogenic
RS2501947501 Health Risk Likely pathogenic Intellectual developmental disorder with autism and macrocephaly, Intellectual developmental disorder with autism and macrocephaly
RS2501953922 Health Risk Likely pathogenic
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