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GCLC mutants [cytosol]
Stable Identifier
R-HSA-5602923
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
cytosol
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective GCLC causes HAGGSD (Homo sapiens)
Defective GCLC does not ligate L-Glu to L-Cys (Homo sapiens)
GCLC mutants:GCLM [cytosol] (Homo sapiens)
GCLC mutants [cytosol] (Homo sapiens)
Participants
members
GCLC H370L [cytosol]
(Homo sapiens)
GCLC P185L [cytosol]
(Homo sapiens)
GCLC R127C [cytosol]
(Homo sapiens)
Participates
as a component of
GCLC mutants:GCLM [cytosol] (Homo sapiens)
Disease
Name
Identifier
Synonyms
hemolytic anemia
DOID:583
Hemolytic anemias (disorder), Hemolytic anemia (disorder), Hemolytic anemias NOS (disorder), hemolytic anemia, ANEMIA HEMOLYTIC
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