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FMO3 mutants [endoplasmic reticulum membrane]
Stable Identifier
R-HSA-5603019
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
endoplasmic reticulum membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective FMO3 causes TMAU (Homo sapiens)
Defective FMO3 does not N-oxidise TMA (Homo sapiens)
FMO3 mutants:FAD [endoplasmic reticulum membrane] (Homo sapiens)
FMO3 mutants [endoplasmic reticulum membrane] (Homo sapiens)
Participants
members
FMO3 E32K [endoplasmic reticulum membrane]
(Homo sapiens)
FMO3 M66I [endoplasmic reticulum membrane]
(Homo sapiens)
FMO3 N61S [endoplasmic reticulum membrane]
(Homo sapiens)
FMO3 P153L [endoplasmic reticulum membrane]
(Homo sapiens)
FMO3 R492W [endoplasmic reticulum membrane]
(Homo sapiens)
Participates
as a component of
FMO3 mutants:FAD [endoplasmic reticulum membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
inherited metabolic disorder
DOID:655
Metabolic hereditary disorder, Inborn Errors of Metabolism, inborn metabolism disorder
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