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Impaired BRCA2 binding to SEM1 (DSS1)
Stable Identifier
R-HSA-9763198
Type
Pathway
Species
Homo sapiens
Compartment
cytosol
ReviewStatus
5/5
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Disease (Homo sapiens)
Diseases of DNA repair (Homo sapiens)
Diseases of DNA Double-Strand Break Repair (Homo sapiens)
Defective homologous recombination repair (HRR) due to BRCA2 loss of function (Homo sapiens)
Impaired BRCA2 binding to SEM1 (DSS1) (Homo sapiens)
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This pathway describes BRCA2 cancer mutations that affect the ability of BRCA2 to bind to SEM1 (DSS1), a small protein of 70 amino acids that regulates BRCA2 stability and its nuclear localization (reviewed in Le et al. 2021).
Literature References
PubMed ID
Title
Journal
Year
34440403
Guardians of the Genome: BRCA2 and Its Partners
Heyer, WD
,
Le, HP
,
Liu, J
Genes (Basel)
2021
Participants
Events
BRCA2 mutants do not bind SEM1 (DSS1)
(Homo sapiens)
Participates
as an event of
Defective homologous recombination repair (HRR) due to BRCA2 loss of function (Homo sapiens)
Disease
Name
Identifier
Synonyms
cancer
DOID:162
malignant tumor, malignant neoplasm, primary cancer
Authored
Orlic-Milacic, M (2022-01-26)
Reviewed
Liu, J (2022-01-26)
Le, HP (2022-01-26)
Heyer, WD (2022-01-26)
Created
Orlic-Milacic, M (2022-01-31)
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