NP_073562.1
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NCBI GenBank Nucleotide #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
42,254 Da
NCBI Official Full Name
Fanconi anemia group F protein
NCBI Official Synonym Full Names
Fanconi anemia complementation group F
NCBI Official Synonym Symbols
NCBI Protein Information
Fanconi anemia group F protein
UniProt Protein Name
Fanconi anemia group F protein
UniProt Synonym Gene Names
UniProt Entry Name
FANCF_HUMAN
NCBI Summary for FANCF
The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group F. [provided by RefSeq, Jul 2008]
UniProt Comments for FANCF
FANCF: DNA repair protein that may operate in a postreplication repair or a cell cycle checkpoint function. May be implicated in interstrand DNA cross-link repair and in the maintenance of normal chromosome stability. Defects in FANCF are the cause of Fanconi anemia complementation group F (FANCF). A disorder affecting all bone marrow elements and resulting in anemia, leukopenia and thrombopenia. It is associated with cardiac, renal and limb malformations, dermal pigmentary changes, and a predisposition to the development of malignancies. At the cellular level it is associated with hypersensitivity to DNA-damaging agents, chromosomal instability (increased chromosome breakage) and defective DNA repair.
Protein type: DNA repair, damage
Chromosomal Location of Human Ortholog: 11p15
Cellular Component: nucleoplasm
Molecular Function: protein binding
Biological Process: ovarian follicle development; protein ubiquitination; spermatogenesis
Disease: Fanconi Anemia, Complementation Group F; Tracheoesophageal Fistula With Or Without Esophageal Atresia
Research Articles on FANCF
Precautions
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Products associated with FANCF blocking peptide
Pathways associated with FANCF blocking peptide
Diseases associated with FANCF blocking peptide
Organs/Tissues associated with FANCF blocking peptide
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