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TPST1,2 [Golgi membrane]
Stable Identifier
R-HSA-8954265
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Golgi membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of hemostasis (Homo sapiens)
Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) (Homo sapiens)
Defective factor VIII causes hemophilia A (Homo sapiens)
Defective F8 sulfation at Y1699 (Homo sapiens)
F8 variant is not sulfonated at Y1699 (Homo sapiens)
TPST1,2 [Golgi membrane] (Homo sapiens)
Metabolism (Homo sapiens)
Biological oxidations (Homo sapiens)
Phase II - Conjugation of compounds (Homo sapiens)
Cytosolic sulfonation of small molecules (Homo sapiens)
TPST1,2 transfer SO4(2-) from PAPS to PODXL2 (Homo sapiens)
TPST1,2 [Golgi membrane] (Homo sapiens)
Metabolism of proteins (Homo sapiens)
Post-translational protein modification (Homo sapiens)
Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation (Homo sapiens)
TPST1,2 transfer SO4(2-) from PAPS to FVIII (Homo sapiens)
TPST1,2 [Golgi membrane] (Homo sapiens)
Participants
members
TPST1 [Golgi membrane]
(Homo sapiens)
TPST2 [Golgi membrane]
(Homo sapiens)
Inferred To
TPST1,2 [Golgi membrane]
(Bos taurus)
TPST1,2 [Golgi membrane]
(Canis familiaris)
TPST1,2 [Golgi membrane]
(Gallus gallus)
TPST1,2 [Golgi membrane]
(Mus musculus)
TPST1,2 [Golgi membrane]
(Rattus norvegicus)
TPST1,2 [Golgi membrane]
(Sus scrofa)
TPST1,2 [Golgi membrane]
(Xenopus tropicalis)
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