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Fanconi Anemia Pathway in DNA repair
Stable Identifier
R-GGA-351465
Type
Pathway
Species
Gallus gallus
Compartment
nucleoplasm
ReviewStatus
5/5
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DNA replication and repair (Gallus gallus)
DNA repair (Gallus gallus)
Fanconi Anemia Pathway in DNA repair (Gallus gallus)
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Fanconi anemia (FA) is a rare human hereditary disorder characterized by bone marrow failure, compromised genomic stability and increased incidence of cancer, due to mutation in any of thirteen genes. The protein products of these genes are involved in DNA repair processes, though the roles for many of them remain to be defined. Three reactions that have been directly characterized in chicken cells, phosphorylation of FANCG, deubiquitination of FANCD2 (BRCA2), and the function of FANCJ (BRIP1) as a helicase, are annotated here.
Participants
Events
Monoubiquitination of FancD2
(Gallus gallus)
Monoubiquitination of FANCI
(Gallus gallus)
Phosphorylation of FANCG at S7
(Gallus gallus)
Deubiquitination of FancD2
(Gallus gallus)
BRIP1 (FANCJ) helicase functions in direct unwinding of DNA
(Gallus gallus)
Participates
as an event of
DNA repair (Gallus gallus)
Event Information
Go Biological Process
DNA repair (0006281)
Authored
Saxena, A (2008-07-07)
Reviewed
Borowiec, JA (2009-04-24)
Created
Saxena, A (2008-05-23)
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