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MUTYH-3 P391L,MUTYH-6 P377L [nucleoplasm]
Stable Identifier
R-HSA-9606705
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of DNA repair (Homo sapiens)
Diseases of Base Excision Repair (Homo sapiens)
Defective Base Excision Repair Associated with MUTYH (Homo sapiens)
Defective MUTYH substrate processing (Homo sapiens)
Defective MUTYH mutants do not cleave adenine mispaired with 8-oxoguanine (Homo sapiens)
MUTYH LOF mutants:(8oxoG:Ade)-dsDNA [nucleoplasm] (Homo sapiens)
MUTYH LOF mutants [nucleoplasm] (Homo sapiens)
MUTYH-3 P391L,MUTYH-6 P377L [nucleoplasm] (Homo sapiens)
Participants
members
MUTYH-3 P391L [nucleoplasm]
(Homo sapiens)
MUTYH-6 P377L [nucleoplasm]
(Homo sapiens)
Participates
as a member of
MUTYH LOF mutants [nucleoplasm] (Homo sapiens)
Disease
Name
Identifier
Synonyms
familial adenomatous polyposis
DOID:0050424
adenomatous polyposis of the colon
colorectal cancer
DOID:9256
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