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SLC5A1 mutants [plasma membrane]
Stable Identifier
R-HSA-5656360
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) (Homo sapiens)
Defective SLC5A1 does not cotransport Glc and Na+ (Homo sapiens)
SLC5A1 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC5A1 D28G [plasma membrane]
(Homo sapiens)
SLC5A1 D28N [plasma membrane]
(Homo sapiens)
SLC5A1 G100V [plasma membrane]
(Homo sapiens)
SLC5A1 Q457R [plasma membrane]
(Homo sapiens)
SLC5A1 R135W [plasma membrane]
(Homo sapiens)
SLC5A1 R379* [plasma membrane]
(Homo sapiens)
SLC5A1 Y191* [plasma membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
glucose intolerance
DOID:10603
Malabsorption of glucose (disorder), Glucose: [intolerance] or [malabsorption]
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