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EXT1:EXT2 mutants [Golgi membrane]
Stable Identifier
R-HSA-9036278
Type
Complex
Species
Homo sapiens
Compartment
Golgi membrane
Locations in the PathwayBrowser
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Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of glycosylation (Homo sapiens)
Diseases associated with glycosaminoglycan metabolism (Homo sapiens)
Defective EXT2 causes exostoses 2 (Homo sapiens)
Defective EXT2 (in EXT1:EXT2) does not transfer GlcA to heparan (Homo sapiens)
EXT1:EXT2 mutants [Golgi membrane] (Homo sapiens)
Defective EXT2 (in EXT1:EXT2) does not transfer GlcNAc to heparan (Homo sapiens)
EXT1:EXT2 mutants [Golgi membrane] (Homo sapiens)
Defective EXT2 (in EXT1:EXT2) does not transfer GlcNAc to the heparan chain (Homo sapiens)
EXT1:EXT2 mutants [Golgi membrane] (Homo sapiens)
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EXT1 [Golgi membrane] (Homo sapiens)
EXT2 mutants [Golgi membrane] (Homo sapiens)
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