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GALNT12 mutants [Golgi membrane]
Stable Identifier
R-HSA-5138165
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 O-glycosylation of proteins (Homo sapiens)
Defective GALNT12 causes CRCS1 (Homo sapiens)
Defective GALNT12 does not transfer GalNAc to mucins (Homo sapiens)
GALNT12 mutants [Golgi membrane] (Homo sapiens)
Participants
members
GALNT12 M1I [Golgi membrane]
(Homo sapiens)
GALNT12 T491M [Golgi membrane]
(Homo sapiens)
GALNT12 Y395* [Golgi membrane]
(Homo sapiens)
GALNT12 D303N [Golgi membrane]
(Homo sapiens)
GALNT12 Y396C [Golgi membrane]
(Homo sapiens)
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