Structured Summary
Abstract
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.
MeSH Record
Classification
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Synonyms
3 entry terms
- FANCN Protein
- PALB2 Protein
- Partner and Localizer of BRCA2 Protein
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2018
MeSH Record
Previous Indexing
- Nuclear Proteins (2006-2017)
- Tumor Suppressor Proteins (2006-2017)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Fanconi Anemia Complementation Group N Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000076164. http://id.nlm.nih.gov/mesh/2026/D000076164
- Fanconi Anemia Complementation Group N Protein. In: Wikidata. https://www.wikidata.org/wiki/Q83138829