Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2036
Gene Symbol: EPB41L1
EPB41L1 		0.600 Biomarker disease GENOMICS_ENGLAND Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients. 25572454 2015
Entrez Id: 2036
Gene Symbol: EPB41L1
EPB41L1 		0.600 GeneticVariation disease UNIPROT Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. 21376300 2011
Entrez Id: 2036
Gene Symbol: EPB41L1
EPB41L1 		0.600 Biomarker disease CTD_human