Gene: TCF20 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 GeneticVariation disease BEFREE De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. 30819258 2019
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 GeneticVariation disease BEFREE Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. 30909959 2019
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 CausalMutation disease CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 CausalMutation disease 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 		0.120 CausalMutation disease 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 		0.120 CausalMutation disease CLINVAR Large-scale discovery of novel genetic causes of developmental disorders. 25533962 2015
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 CausalMutation disease 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 		0.120 CausalMutation disease CLINVAR Discovery of transcription factors and other candidate regulators of neural crest development. 18351660 2008
Entrez Id: 6942
Gene Symbol: TCF20
TCF20 		0.120 CausalMutation disease CLINVAR Genome-wide atlas of gene expression in the adult mouse brain. 17151600 2007