Gene: CHD8 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 CausalMutation phenotype CLINVAR A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. 26789910 2016
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 GeneticVariation phenotype CLINVAR A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review. 26789910 2016
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 GeneticVariation phenotype CLINVAR Disruptive CHD8 mutations define a subtype of autism early in development. 24998929 2014
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 CausalMutation phenotype CLINVAR Disruptive CHD8 mutations define a subtype of autism early in development. 24998929 2014
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 GeneticVariation phenotype CLINVAR Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. 23160955 2012
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 CausalMutation phenotype CLINVAR Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. 22495309 2012
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 GeneticVariation phenotype CLINVAR Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. 22495309 2012
Entrez Id: 57680
Gene Symbol: CHD8
CHD8 		0.100 CausalMutation phenotype CLINVAR Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. 23160955 2012