×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
CLINVAR
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CTD_human
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Cancer susceptibility of mice with a homozygous deletion in the COOH-terminal domain of the Brca2 gene.
11861370
2002
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
Biallelic inactivation of BRCA2 in Fanconi anemia.
12065746
2002
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
UNIPROT
Biallelic inactivation of BRCA2 in Fanconi anemia.
12065746
2002
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Biallelic inactivation of BRCA2 in Fanconi anemia.
12065746
2002
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
BEFREE
The breast cancer susceptibility gene BRCA2 was recently found to be associated with Fanconi anemia complementation group D1 (FA-D1 ).
14559878
2003
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
UNIPROT
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.
14670928
2004
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.
14670928
2004
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GermlineCausalMutation
disease
ORPHANET
Association of biallelic BRCA2/FANCD1 mutations with spontaneous chromosomal instability and solid tumors of childhood.
14670928
2004
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia.
15070707
2004
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GermlineCausalMutation
disease
ORPHANET
Biallelic BRCA2 mutations are associated with multiple malignancies in childhood including familial Wilms tumour.
15689453
2005
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
UNIPROT
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
16825431
2007
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GermlineCausalMutation
disease
ORPHANET
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
16825431
2007
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.
16825431
2007
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1.
16859999
2006
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
MGD
Hematopoietic dysfunction in a mouse model for Fanconi anemia group D1.
16859999
2006
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
UNIPROT
A comprehensive functional characterization of BRCA2 variants associated with Fanconi anemia using mouse ES cell-based assay.
21719596
2011
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
UNIPROT
A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activity.
23108138
2013
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
23788249
2013
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
A novel splice site mutation in the noncoding region of BRCA2: implications for Fanconi anemia and familial breast cancer diagnostics.
24395671
2014
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
GeneticVariation
disease
BEFREE
Fanconi anemia, complementation group D1 with bi-allelic FANCD1 (BRCA2 ) mutations, is a very rare genetic disorder characterized by early onset of childhood malignancies, including acute leukemia, brain cancer and nephroblastoma.
26657402
2016
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
GENOMICS_ENGLAND
Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
28185119
2017
×
Entrez Id:
675
Gene Symbol:
BRCA2
BRCA2
0.920
Biomarker
disease
CLINGEN
Fanconi anaemia and cancer: an intricate relationship.
29376519
2018