CHST3 R222W [Golgi membrane]

Stable Identifier
R-HSA-3636785
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Carbohydrate sulfotransferase 3, CHST3_HUMAN
CHST3 R222W [Golgi membrane] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CHST3
Chain
chain:1-479
Other Identifiers
11721191_at
11721192_at
11721193_at
16705934
208252_PM_s_at
208252_s_at
209834_PM_at
209834_at
32094_PM_at
32094_at
3251299
3251308
3251309
3251310
3251311
3251312
3251313
7928291
9469
A_14_P134605
GE53432
GO:0000139
GO:0001517
GO:0002376
GO:0003824
GO:0005794
GO:0005802
GO:0005975
GO:0006044
GO:0006790
GO:0008146
GO:0008459
GO:0016020
GO:0016740
GO:0030206
GO:0043029
GO:0043226
GO:0050698
GO:1901135
HMNXSV003020538
ILMN_1723481
PH_hs_0009584
TC10000445.hg
g4115403_3p_s_at
g4757985_3p_a_at
g4757985_3p_s_at
Participates
Other forms of this molecule
Modified Residues
Name
L-arginine 222 replaced with L-tryptophan
Coordinate
222
PsiMod
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
osteochondrodysplasia DOID:2256 Unspecified anomaly of cartilage (disorder), chondrodystrophy, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome (disorder), Cartilage Development disorder
Cross References
OpenTargets
GeneCards
PRO
Pharos - Targets
Orphanet
HMDB Protein
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