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sucrase-isomaltase Q1098P [plasma membrane]
Stable Identifier
R-HSA-5659906
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of carbohydrate metabolism (Homo sapiens)
Intestinal saccharidase deficiencies (Homo sapiens)
Defective SI does not hydrolyze Mal (Homo sapiens)
SI mutant dimers [plasma membrane] (Homo sapiens)
sucrase-isomaltase dimer Q1098P [plasma membrane] (Homo sapiens)
sucrase-isomaltase Q1098P [plasma membrane] (Homo sapiens)
Defective SI does not hydrolyze Suc (Homo sapiens)
SI mutant dimers [plasma membrane] (Homo sapiens)
sucrase-isomaltase dimer Q1098P [plasma membrane] (Homo sapiens)
sucrase-isomaltase Q1098P [plasma membrane] (Homo sapiens)
Defective SI does not hydrolyze iMal (Homo sapiens)
SI mutant dimers [plasma membrane] (Homo sapiens)
sucrase-isomaltase dimer Q1098P [plasma membrane] (Homo sapiens)
sucrase-isomaltase Q1098P [plasma membrane] (Homo sapiens)
Defective SI does not hydrolyze maltotriose (Homo sapiens)
SI mutant dimers [plasma membrane] (Homo sapiens)
sucrase-isomaltase dimer Q1098P [plasma membrane] (Homo sapiens)
sucrase-isomaltase Q1098P [plasma membrane] (Homo sapiens)
Participants
components
SI(1-1006) [plasma membrane]
(Homo sapiens)
SI(1007-1826) Q1098P [plasma membrane]
(Homo sapiens)
Participates
as a component of
sucrase-isomaltase dimer Q1098P [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
intestinal disaccharidase deficiency
DOID:9868
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