Search
Descriptor English: Fanconi Anemia Complementation Group N Protein
Descriptor Spanish: Proteína del Grupo de Complementación N de la Anemia de Fanconi
Descriptor proteína del grupo de complementación N de la anemia de Fanconi 
Entry term(s) proteína FANCN
proteína PALB2
socio y localizador de BRCA2
Scope note: Proteína del grupo de complementación de la anemia de Fanconi que contiene una región de unión a ADN aminoterminal y siete REPETICIONES WD carboxiterminales. Es un factor esencial para la REPARACIÓN DEL ADN POR RECOMBINACIÓN HOMÓLOGA mediante su interacción con la PROTEÍNA BRCA2, la RECOMBINASA RAD51 y la PROTEÍNA BRCA1. Funciona como andamio molecular para localizar y estabilizar estas proteínas en los sitios de recombinación homóloga. Las mutaciones en el gen PALB2 se asocian al grupo de complementación N de la ANEMIA DE FANCONI, NEOPLASIAS PANCREÁTICAS de tipo 3 y a susceptibilidad al CÁNCER DE MAMA.
Descriptor Portuguese: Proteína do Grupo de Complementação N da Anemia de Fanconi
Descriptor French: Protéine du groupe de complémentation N de l'anémie de Fanconi
Entry term(s): FANCN Protein
PALB2 Protein
Partner and Localizer of BRCA2 Protein
Tree number(s): D12.776.313.953
D12.776.624.776.051
D12.776.660.323
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000076164
Scope note: 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.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Previous Indexing: Nuclear Proteins (2006-2017)
Tumor Suppressor Proteins (2006-2017)
Public MeSH Note: 2018
History Note: 2018
DeCS ID: 57122
Unique ID: D000076164
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2018/01/01
Date of Entry: 2017/07/11
Revision Date: 2017/06/29
Fanconi Anemia Complementation Group N Protein - Preferred
Concept UI M000632389
Scope note 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.
Preferred term Fanconi Anemia Complementation Group N Protein
Entry term(s) FANCN Protein
PALB2 Protein
Partner and Localizer of BRCA2 Protein



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey