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SLC26A2 mutants [plasma membrane]
Stable Identifier
R-HSA-3621736
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of glycosylation (Homo sapiens)
Diseases associated with glycosaminoglycan metabolism (Homo sapiens)
Defective SLC26A2 causes chondrodysplasias (Homo sapiens)
Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol (Homo sapiens)
SLC26A2 mutants [plasma membrane] (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective SLC26A2 causes chondrodysplasias (Homo sapiens)
Defective SLC26A2 does not cotransport extracellular SO4(2-), H+ to cytosol (Homo sapiens)
SLC26A2 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC26A2 N425D [plasma membrane]
(Homo sapiens)
SLC26A2 R178* [plasma membrane]
(Homo sapiens)
SLC26A2 G255E [plasma membrane]
(Homo sapiens)
SLC26A2 L483P [plasma membrane]
(Homo sapiens)
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