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SLC1A1 mutants [plasma membrane]
Stable Identifier
R-HSA-5625024
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 SLC1A1 is implicated in schizophrenia 18 (SCZD18) and dicarboxylic aminoaciduria (DCBXA) (Homo sapiens)
SLC1A1 does not cotransport L-Glu,L-Asp,D-Asp,H+,3Na+ from extracellular region to cytosol (Homo sapiens)
SLC1A1 mutants [plasma membrane] (Homo sapiens)
Participants
members
SLC1A1 84kb_del [plasma membrane]
(Homo sapiens)
SLC1A1 I395del [plasma membrane]
(Homo sapiens)
SLC1A1 R445W [plasma membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
schizophrenia
DOID:5419
schizophrenia-1
amino acid metabolic disorder
DOID:9252
inborn errors of amino acid metabolism
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