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SLC22A18 mutants [plasma membrane]
Stable Identifier
R-HSA-5625599
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 SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1) (Homo sapiens)
Defective SLC22A18 does not exchange extracellular organic cations for cytosolic H+ (Homo sapiens)
SLC22A18 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC22A18 R286H [plasma membrane] (Homo sapiens)
SLC22A18 S233F [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
rhabdomyosarcoma
3247
Rhabdomyosarcoma NOS (morphologic abnormality), rhabdomyosarcoma, Rhabdomyosarcoma, no subtype (morphologic abnormality), rhabdomyoblastoma, Rhabdomyosarcoma (disorder)
lung cancer
1324
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