Gene: TBR1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 GeneticVariation disease BEFREE In humans, de novo mutations in TBR1 are important causes of sporadic autism and intellectual disability. 28057268 2017
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 GeneticVariation disease BEFREE Because TBR1 is critical for glutamate receptor, ionotropic, <i>N</i>-methyl-D-aspartate receptor subunit 2B (<i>Grin2b</i>) expression and is a causative gene for autism and intellectual disability, we then generated CASK T740A (corresponding to rat CASK T724A) mutant mice using a gene-targeting approach. 28234597 2017
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 Biomarker disease BEFREE TBR1 regulates autism risk genes in the developing neocortex. 27325115 2016
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 GeneticVariation disease BEFREE Here we demonstrate the power of the approach, performing the first functional analyses of TBR1 variants identified in sporadic autism. 25232744 2014
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 Biomarker disease BEFREE In humans, PAX6, EOMES, and TBR1 have been linked to intellectual disability and autism. 23431145 2013
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 Biomarker disease GENOMICS_ENGLAND Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. 23160955 2012
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 Biomarker disease CTD_human
Entrez Id: 10716
Gene Symbol: TBR1
TBR1 		0.650 Biomarker disease HPO