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C19orf40 wt Allele

Known as: FLJ46828, Fanconi Anemia-Associated Protein, 24kDa Gene, Chromosome 19 Open Reading Frame 40 wt Allele 
Human C19orf40 wild-type allele is located in the vicinity of 19q13.11 and is approximately 5 kb in length. This allele, which encodes Fanconi anemia… 
National Institutes of Health

Related topics

Related topics

3 relations
DNA Repairdna binding

Broader (1)

FAAP24 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
2 Inflammatory ROS in Fanconi Anemia Hematopoiesis and Leukemogenesis
  • 2018
  • Corpus ID: 53598097
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem… 
2013
2013
The Fanconi anemia associated protein FAAP24 uses two substrate specific binding surfaces for DNA recognition
To maintain the integrity of the genome, multiple DNA repair systems exist to repair damaged DNA. Recognition of altered DNA… 
2013
2013
Solution Structure of ERCC4 domain of human FAAP24
2012
2012
Inflammatory ROS in Fanconi Anemia Hematopoiesis and Leukemogenesis
  • 2012
  • Corpus ID: 35183933
Fanconi anemia (FA) is a genetic disorder characterized by bone marrow failure (BMF), clonal proliferation of hematopoietic stem… 
Review
2009
Review
2009
FANCM-FAAP24 and FANCJ: FA proteins that metabolize DNA.
2008
2008
Cell cycle-dependent chromatin loading of the Fanconi anemia core complex by FANCM/FAAP24. Commentary
Fanconi anemia (FA) is a genetic disease characterized by congenital abnormalities, bone marrow failure, and cancer… 
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