Fanconi Anemia Complementation Group A Protein
"Fanconi Anemia Complementation Group A Protein" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A Fanconi anemia complementation group protein that is the most commonly mutated protein in FANCONI ANEMIA. It undergoes PHOSPHORYLATION by PROTEIN KINASE B and forms a complex with FANCC PROTEIN in the CELL NUCLEUS.
| Descriptor ID |
D052217
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| MeSH Number(s) |
D12.776.313.500 D12.776.660.264 D12.776.744.476
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Fanconi Anemia Complementation Group A Protein".
Below are MeSH descriptors whose meaning is more specific than "Fanconi Anemia Complementation Group A Protein".
This graph shows the total number of publications written about "Fanconi Anemia Complementation Group A Protein" by people in this website by year, and whether "Fanconi Anemia Complementation Group A Protein" was a major or minor topic of these publications.
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Below are the most recent publications written about "Fanconi Anemia Complementation Group A Protein" by people in Profiles.
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Genetic variants in fanconi anemia pathway genes BRCA2 and FANCA predict melanoma survival. J Invest Dermatol. 2015 Feb; 135(2):542-550.
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Fanconi anemia (FA) binding protein FAAP20 stabilizes FA complementation group A (FANCA) and participates in interstrand cross-link repair. Proc Natl Acad Sci U S A. 2012 Mar 20; 109(12):4491-6.