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SLC2A9 mutants [plasma membrane]
Stable Identifier
R-HSA-5638215
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 SLC2A9 causes hypouricemia renal 2 (RHUC2) (Homo sapiens)
Defective SLC2A9 does not transport Fru, Glc, urate (Homo sapiens)
SLC2A9 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC2A9 G216R [plasma membrane]
(Homo sapiens)
SLC2A9 L75R [plasma membrane]
(Homo sapiens)
SLC2A9 R171C [plasma membrane]
(Homo sapiens)
SLC2A9 R198C [plasma membrane]
(Homo sapiens)
SLC2A9 R380W [plasma membrane]
(Homo sapiens)
SLC2A9 T125M [plasma membrane]
(Homo sapiens)
SLC2A9 W23* [plasma membrane]
(Homo sapiens)
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