Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719

2017
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth. 27436265

2016
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability. 27479843

2016
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR Large-scale discovery of novel genetic causes of developmental disorders. 25533962

2015
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder. 25228304

2014
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR Discovery of transcription factors and other candidate regulators of neural crest development. 18351660

2008
Entrez Id: 6942
Gene Symbol: TCF20
TCF20
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.120 CausalMutation CLINVAR Genome-wide atlas of gene expression in the adult mouse brain. 17151600

2007