Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Fanconi anaemia and cancer: an intricate relationship. 29376519

2018
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia. 12913077

2003
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa. 11344308

2001
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Mice with a targeted disruption of the Fanconi anemia homolog Fanca. 10915769

2000
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Spontaneous functional correction of homozygous fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism. 10431244

1999
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) 		1.000 Biomarker CLINGEN Positional cloning of the Fanconi anaemia group A gene. 8896564

1996