FANCG, FA complementation group G, 2189

N. diseases: 132; N. variants: 19
Disease: fanconi anemia complementation group g ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN Fanconi anaemia and cancer: an intricate relationship. 29376519 2018
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR Targeted resequencing of 52 bone marrow failure genes in patients with aplastic anemia reveals an increased frequency of novel variants of unknown significance only in SLX4. 24763404 2014
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia. 23613520 2013
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia. 20606166 2010
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease GENOMICS_ENGLAND How the fanconi anemia pathway guards the genome. 19686080 2009
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 GeneticVariation disease UNIPROT HES1 is a novel interactor of the Fanconi anemia core complex. 18550849 2008
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease GENOMICS_ENGLAND Molecular pathogenesis of Fanconi anemia: recent progress. 16493006 2006
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR A common Fanconi anemia mutation in black populations of sub-Saharan Africa. 15657175 2005
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study. 12552564 2003
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR Spectrum of sequence variation in the FANCG gene: an International Fanconi Anemia Registry (IFAR) study. 12552564 2003
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice. 11823446 2002
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN Targeted disruption of the murine Fanconi anemia gene, Fancg/Xrcc9. 11719385 2001
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 GeneticVariation disease UNIPROT Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. 11093276 2000
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9. 11093276 2000
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease GENOMICS_ENGLAND The Fanconi anaemia group G gene FANCG is identical with XRCC9. 9806548 1998
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CLINGEN The Fanconi anaemia group G gene FANCG is identical with XRCC9. 9806548 1998
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 CausalMutation disease CLINVAR The Fanconi anaemia group G gene FANCG is identical with XRCC9. 9806548 1998
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease CTD_human
CUI: C3469527
Disease: fanconi anemia complementation group g
fanconi anemia complementation group g 		0.700 Biomarker disease GENOMICS_ENGLAND