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SLC34A2 mutants [plasma membrane]
Stable Identifier
R-HSA-5651683
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 SLC34A2 causes pulmonary alveolar microlithiasis (PALM) (Homo sapiens)
Defective SLC34A2 does not cotransport Pi, 3Na+ (Homo sapiens)
SLC34A2 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC34A2 G106R [plasma membrane]
(Homo sapiens)
SLC34A2 K304* [plasma membrane]
(Homo sapiens)
SLC34A2 Q76* [plasma membrane]
(Homo sapiens)
SLC34A2 N38Tfs*8 [plasma membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
pulmonary alveolar microlithiasis
DOID:12117
pulmonary alveolar microlithiasis (disorder)
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