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SLC16A1 mutants:BSG [plasma membrane]
Stable Identifier
R-HSA-9645219
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
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Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT) (Homo sapiens)
Defective SLC16A1 does not cotransport monocarboxylates, H+ from extracellular region to cytosol (Homo sapiens)
SLC16A1 mutants:BSG [plasma membrane] (Homo sapiens)
Participants
components
BSG [plasma membrane]
(Homo sapiens)
SLC16A1 mutants [plasma membrane]
(Homo sapiens)
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