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Fanconi Anemia Complementation Group N Protein

A Fanconi anemia complementation group protein that contains an N-terminal DNA-binding region and seven, C-terminal, WD REPEATS. It is an essential factor in HOMOLOGOUS RECOMBINATION DNA REPAIR through its interactions with BRCA2 PROTEIN; RAD51 RECOMBINASE; and BRCA1 PROTEIN. It functions as a molecular scaffold to localize and stabilize these proteins at homologous recombination sites. Mutations in the PALB2 gene are associated with FANCONI ANEMIA complementation group N; type 3 PANCREATIC NEOPLASMS; and susceptibility to BREAST CANCER.
Also Known As:
FANCN Protein; PALB2 Protein; Partner and Localizer of BRCA2 Protein
Networked: 5 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Eshleman, James R: 2 articles (01/2011 - 04/2009)
2. Hruban, Ralph H: 2 articles (01/2011 - 04/2009)
3. Jones, Siân: 2 articles (01/2011 - 04/2009)
4. Maitra, Anirban: 2 articles (01/2011 - 04/2009)
5. Brahiti, Nadine: 1 article (01/2019)
6. Dellaire, Graham: 1 article (01/2019)
7. Deveryshetty, Jaigeeth: 1 article (01/2019)
8. Korolev, Sergey: 1 article (01/2019)
9. Masson, Jean-Yves: 1 article (01/2019)
10. Peterlini, Thibaut: 1 article (01/2019)

Related Diseases

1. Fanconi Anemia (Fanconi's Anemia)
2. Breast Neoplasms (Breast Cancer)
3. Neoplasms (Cancer)
4. Familial Breast Cancer

Related Drugs and Biologics

1. Proteins (Proteins, Gene)
2. DNA (Deoxyribonucleic Acid)