Gene Ontology annotation through association of InterPro records with GO terms
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
X-linked inheritance of Fanconi anemia complementation group B.
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
The Fanconi anemia pathway promotes replication-dependent DNA interstrand cross-link repair.
A histone-fold complex and FANCM form a conserved DNA-remodeling complex to maintain genome stability.
The phenotype of FancB-mutant mouse embryonic stem cells.
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway.
The FA Core Complex Contains a Homo-dimeric Catalytic Module for the Symmetric Mono-ubiquitination of FANCI-FANCD2.
Structure of the Fanconi anaemia monoubiquitin ligase complex.
Association of clinical severity with FANCB variant type in Fanconi anemia.
Deep learning enables the atomic structure determination of the Fanconi Anemia core complex from cryoEM.
FA core complex assembles at DNA interstrand crosslinks (ICLs)
FANCD2:FANCI complex and UBE2T bind ICL-DNA associated with the FA core complex
Monoubiquitination of FANCD2:FANCI
DNA nucleases bind monoubiquitinated ID2 complex
DNA nucleases unhook the interstrand crosslink (ICL)
Translesion synthesis across unhooked ICL by POLN
FANCD2 deubiquitination by USP1:WDR48
The complex of ATR and ATRIP is recruited to ICL-DNA
ATR phosphorylates RPA2, FANCI, FANCD2 and FANCM at ICL-DNA
FA core complex:HSP70s binds PKR