Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 GeneticVariation disease BEFREE Summary of literature data describing heterozygous loss-of-function variants in DCC (n = 61) revealed 63.9% penetrance for mirror movements, 9.8% for ACC, and 5% for both. 31697046 2020
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 GeneticVariation disease BEFREE Group I contains three DCC missense variants that are rather unlikely to be associated with a higher risk to CMM and/or ACC. 29366874 2018
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 CausalMutation disease CLINVAR Biallelic mutations in human DCC cause developmental split-brain syndrome. 28250456 2017
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 Biomarker disease CTD_human DCC mutations result in variable dominant phenotypes with decreased penetrance, including mirror movements and ACC associated with a favorable developmental prognosis. 28250454 2017
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 GeneticVariation disease BEFREE DCC mutations result in variable dominant phenotypes with decreased penetrance, including mirror movements and ACC associated with a favorable developmental prognosis. 28250454 2017
Entrez Id: 1630
Gene Symbol: DCC
DCC
0.430 Biomarker disease HPO