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CUBN P1297L:AMN [plasma membrane]
Stable Identifier
R-HSA-5654976
Type
Complex
Species
Homo sapiens
Compartment
plasma membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Defects in vitamin and cofactor metabolism (Homo sapiens)
Defects in cobalamin (B12) metabolism (Homo sapiens)
Defective CUBN causes MGA1 (Homo sapiens)
Defective CUBN does not transport GIF:Cbl (Homo sapiens)
CUBN P1297L:AMN [plasma membrane] (Homo sapiens)
Participants
components
AMN [plasma membrane]
(Homo sapiens)
CUBN P1297L [plasma membrane]
(Homo sapiens)
Participates
as an input of
Defective CUBN does not transport GIF:Cbl (Homo sapiens)
Disease
Name
Identifier
Synonyms
megaloblastic anemia
DOID:13382
megaloblastic anemia, Megaloblastic anemia (disorder), Anaemia - megaloblastic, Megaloblastic anemia NOS (disorder), Megaloblastic anaemia, ANEMIA MEGALOBLASTIC, Megaloblastic anemia NOS, Megaloblastic Anemia, Megaloblastic anemia NOS (disorder), Anaemia - megaloblastic, Megaloblastic anemia, NOS, Megaloblastic anemia NOS
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