Gene: MED13L ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 CausalMutation disease CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886 2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 CausalMutation disease CLINVAR Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. 23403903 2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 GeneticVariation disease CLINVAR Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. 23403903 2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 GeneticVariation disease CLINVAR Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. 24267886 2013
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 GeneticVariation disease CLINVAR Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries). 14638541 2003
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 CausalMutation disease CLINVAR Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries). 14638541 2003
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 CausalMutation disease CLINVAR [Criteria in the evaluation of blood picture for the diagnosis of bovine leukosis]. 5167861 1971
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.110 GeneticVariation disease CLINVAR [Criteria in the evaluation of blood picture for the diagnosis of bovine leukosis]. 5167861 1971