Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene. 17200668

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 GeneticVariation CLINVAR Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer. 17200671

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Fanconi anemia is associated with a defect in the BRCA2 partner PALB2. 17200672

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR A recurrent mutation in PALB2 in Finnish cancer families. 17287723

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Analysis of PALB2/FANCN-associated breast cancer families. 17420451

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women. 18053174

2007

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families. 18302019

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR The prevalence of PALB2 germline mutations in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives. 18446436

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Penetrance analysis of the PALB2 c.1592delT founder mutation. 18628482

2008

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. 19264984

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 GeneticVariation CLINVAR Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene. 19264984

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR The breast cancer susceptibility mutation PALB2 1592delT is associated with an aggressive tumor phenotype. 19383810

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 GeneticVariation CLINVAR Structural basis for recruitment of BRCA2 by PALB2. 19609323

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR Structural basis for recruitment of BRCA2 by PALB2. 19609323

2009

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR A PALB2 germline mutation associated with hereditary breast cancer in Italy. 19763884

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR A novel germline PALB2 deletion in Polish breast and ovarian cancer patients. 20122277

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2 mutations in European familial pancreatic cancer families. 20412113

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2 analysis in BRCA2-like families. 20582465

2011

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2: a novel inactivating mutation in a Italian breast cancer family. 20852946

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 GeneticVariation CLINVAR Cooperation of breast cancer proteins PALB2 and piccolo BRCA2 in stimulating homologous recombination. 20871615

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2 mutations in German and Russian patients with bilateral breast cancer. 21165770

2011

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 GeneticVariation CLINVAR PALB2 mutations in German and Russian patients with bilateral breast cancer. 21165770

2011

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR A PALB2 mutation associated with high risk of breast cancer. 21182766

2010

Entrez Id: 79728
Gene Symbol: PALB2
PALB2
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0.100 CausalMutation CLINVAR PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer. 21184274

2011