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SLC3A1 mutants [plasma membrane]
Stable Identifier
R-HSA-5655729
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 SLC3A1 causes cystinuria (CSNU) (Homo sapiens)
Defective SLC3A1 (in SLC7A9:SLC3A1) does not exchange L-Arg, CySS-, L-Lys for L-Leu (Homo sapiens)
SLC3A1 mutants:SLC7A9 [plasma membrane] (Homo sapiens)
SLC3A1 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC3A1 L678P [plasma membrane]
(Homo sapiens)
SLC3A1 M467K [plasma membrane]
(Homo sapiens)
SLC3A1 M467T [plasma membrane]
(Homo sapiens)
SLC3A1 P615T [plasma membrane]
(Homo sapiens)
SLC3A1 R181Q [plasma membrane]
(Homo sapiens)
SLC3A1 Y533N [plasma membrane]
(Homo sapiens)
Participates
as a component of
SLC3A1 mutants:SLC7A9 [plasma membrane] (Homo sapiens)
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