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LCT mutant dimers [plasma membrane]
Stable Identifier
R-HSA-5657985
Type
Set [DefinedSet]
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 LCT does not hydrolyze Lac (Homo sapiens)
LCT mutant dimers [plasma membrane] (Homo sapiens)
Participants
members
LCT G1363S dimer [plasma membrane]
(Homo sapiens)
LCT R1587H dimer [plasma membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
lactose intolerance
DOID:10604
LM - Lactose malabsorption
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