Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR FANCM c.5101C>T mutation associates with breast cancer survival and treatment outcome. 27542569

2016
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR Identification of point mutations and large intragenic deletions in Fanconi anemia using next-generation sequencing technology. 26740942

2015
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR Distribution and medical impact of loss-of-function variants in the Finnish founder population. 25078778

2014
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer. 25288723

2014
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M. 19423727

2009
Entrez Id: 57697
Gene Symbol: FANCM
FANCM
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		0.700 SusceptibilityMutation CLINVAR Our data suggest an evolutionary link between Fanconi anemia-associated proteins and DNA repair; FANCM may act as an engine that translocates the Fanconi anemia core complex along DNA. 16116422

2005