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 		0.700 CausalMutation disease CLINVAR De novo genic mutations among a Chinese autism spectrum disorder cohort. 27824329 2016
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.700 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 		0.700 GeneticVariation disease UNIPROT 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 		0.700 Biomarker disease CTD_human
Entrez Id: 23389
Gene Symbol: MED13L
MED13L 		0.700 Biomarker disease GENOMICS_ENGLAND