CHST3 L307P [Golgi membrane]

Stable Identifier
R-HSA-3636832
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Carbohydrate sulfotransferase 3, CHST3_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
CHST3
Chain
chain:1-479
Other Identifiers
0006290132
11721191_at
11721192_at
11721193_at
16705934
208252_s_at
209834_at
32094_at
3251299
3251308
3251309
3251310
3251311
3251312
3251313
7928291
9469
A_14_P134605
GE53432
GO:0000139
GO:0001517
GO:0003674
GO:0005575
GO:0005622
GO:0005737
GO:0005794
GO:0005802
GO:0005975
GO:0006044
GO:0006790
GO:0008146
GO:0008150
GO:0008459
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0030206
GO:0043226
GO:0044281
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-leucine 307 replaced with L-proline
Coordinate
307
PsiMod
A protein modification that effectively converts a source amino acid residue to L-proline.
A protein modification that effectively removes or replaces an L-leucine.
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
GlyGen
HMDB Protein
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