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SLC27A4 mutants [plasma membrane]
Stable Identifier
R-HSA-5627903
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 SLC27A4 causes ichthyosis prematurity syndrome (IPS) (Homo sapiens)
Defective SLC27A4 does not transport LCFAs from extracellular region to cytosol (Homo sapiens)
SLC27A4 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC27A4 A92T [plasma membrane]
(Homo sapiens)
SLC27A4 C168* [plasma membrane]
(Homo sapiens)
SLC27A4 Q300R [plasma membrane]
(Homo sapiens)
SLC27A4 R583H [plasma membrane]
(Homo sapiens)
SLC27A4 S247P [plasma membrane]
(Homo sapiens)
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