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ST3GAL3 mutants [Golgi membrane]
Stable Identifier
R-HSA-3702117
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Golgi membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of glycosylation (Homo sapiens)
Diseases associated with glycosaminoglycan metabolism (Homo sapiens)
Defective ST3GAL3 causes MCT12 and EIEE15 (Homo sapiens)
Defective ST3GAL3 does not transfer SA to keratan (Homo sapiens)
ST3GAL3 mutants [Golgi membrane] (Homo sapiens)
Participants
members
ST3GAL3 A13D [Golgi membrane]
(Homo sapiens)
ST3GAL3 D370Y [Golgi membrane]
(Homo sapiens)
ST3GAL3 A320P [Golgi membrane]
(Homo sapiens)
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