CHST3 L259P

Stable Identifier
R-HSA-3636789
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
47523
55704
7928291
9469
A_14_P134605
AAH93690
AAI04857
AB012192
AB017915
BAA32576
BAA36348
BC093690
BC104856
CCDS7312
CHST3
CHST3-201
ENSG00000122863
ENSP00000362207
ENST00000373115
EntrezGene:9469
g4115403_3p_s_at
g4757985_3p_a_at
g4757985_3p_s_at
GE53432
GO:0000139
GO:0001517
GO:0003674
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005794
GO:0005975
GO:0006790
GO:0008146
GO:0008150
GO:0008459
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0030206
GO:0043226
GO:0044281
HGNC:1971
HPA047523
HPA055704
ILMN_1723481
IPR000863
IPR016469
IPR027417
MIM:143095
MIM:245600
MIM:603799
NM_004273
NP_004264
PF00685
PH_hs_0009584
TC10000445.hg
uc001jsn.4
UPI000013CB04
XM_006718075
XM_011540369
XP_006718138
XP_011538671
Participant Of
Other forms of this molecule
Modified Residues
Name
L-leucine 259 replaced with L-proline
Coordinate
259
PsiMod HEY
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 2256 Unspecified anomaly of cartilage (disorder), chondrodystrophy, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome (disorder), Cartilage Development disorder
Cross References
GeneCards
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein