Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 GeneticVariation disease BEFREE NBN germ line mutations were not significantly associated with BC risk (OR:1.39, 95%CI: 0.73-2.64). 29522266 2018
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease CLINGEN Proteomics. Tissue-based map of the human proteome. 25613900 2015
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease BEFREE Rarity of "second-hit" inactivation of the involved gene in CHEK2-, NBN/NBS1- and BLM-associated BC demonstrates their substantial biological difference from BRCA1/2-driven cancers and makes them poorly suitable for the clinical trials with cisplatin and PARP inhibitors. 24415413 2014
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 GeneticVariation disease BEFREE CtIP plays an important role in homologous recombination (HR)-mediated DNA double-stranded break (DSB) repair and interacts with Nbs1 and BRCA1, which are linked to Nijmegen breakage syndrome (NBS) and familial breast cancer, respectively. 23468639 2013
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease CLINGEN Significant association between Nijmegen breakage syndrome 1 657del5 polymorphism and breast cancer risk. 23765759 2013
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease BEFREE Our results exclude the possible role of RAD50 and NBS1 in familial breast cancer predisposition in Chinese women, and there is no evidence for the recommendation of RAD50 and NBS1 for genetic testing in China. 21811815 2012
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease CLINGEN Targeted disruption of NBS1 reveals its roles in mouse development and DNA repair. 11889050 2002
Entrez Id: 4683
Gene Symbol: NBN
NBN
0.340 Biomarker disease CLINGEN ATM-dependent phosphorylation of nibrin in response to radiation exposure. 10802669 2000