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CHST6 mutants [Golgi membrane]
Stable Identifier
R-HSA-3656442
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 CHST6 causes MCDC1 (Homo sapiens)
Defective CHST6 does not transfer SO4(2-) to GlcNAc residues on keratan-PG (Homo sapiens)
CHST6 mutants [Golgi membrane] (Homo sapiens)
Participants
members
CHST6 C102G [Golgi membrane]
(Homo sapiens)
CHST6 D203E [Golgi membrane]
(Homo sapiens)
CHST6 E274K [Golgi membrane]
(Homo sapiens)
CHST6 K174R [Golgi membrane]
(Homo sapiens)
CHST6 L200R [Golgi membrane]
(Homo sapiens)
CHST6 L276P [Golgi membrane]
(Homo sapiens)
CHST6 R211W [Golgi membrane]
(Homo sapiens)
CHST6 Y110C [Golgi membrane]
(Homo sapiens)
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