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Fanconi anemia, complementation group C
Protein-coding gene in the species Homo sapiens / From Wikipedia, the free encyclopedia
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Fanconi anemia group C protein is a protein that in humans is encoded by the FANCC gene.[5][6] This protein delays the onset of apoptosis and promotes homologous recombination repair of damaged DNA. Mutations in this gene result in Fanconi anemia, a human rare disorder characterized by cancer susceptibility and cellular sensitivity to DNA crosslinks and other damages.[6][7]
Quick Facts FANCC, Identifiers ...
FANCC | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | FANCC, Fancc, Facc, FA3, FAC, mir-3074-1, FACC, Fanconi anemia complementation group C, FA complementation group C | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 613899; MGI: 95480; HomoloGene: 109; GeneCards: FANCC; OMA:FANCC - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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