EXT2 Y222* [Golgi membrane]

Stable Identifier
R-HSA-3731060
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Exostosin-2, EXT2_HUMAN
EXT2 Y222* [Golgi membrane] icon
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
EXT2
Chain
chain:1-718
Other Identifiers
11723014_a_at
11723015_s_at
11752434_a_at
11752435_s_at
16724031
202012_PM_s_at
202012_s_at
202013_PM_s_at
202013_s_at
2132
235685_PM_at
235685_at
236483_PM_at
236483_at
3328390
3328391
3328392
3328393
3328394
3328396
3328397
3328400
3328401
3328402
3328403
3328404
3328405
3328409
3328410
3328415
3328416
3328420
3328427
3328428
3328429
3328431
3328432
3328433
3328434
3328454
3328455
3328456
3328457
3328458
3328460
3328462
36593_at
36594_s_at
54876_at
57976_at
7939524
A_14_P102151
A_14_P103622
A_14_P104744
A_23_P13183
A_32_P27373
GE58218
GE854284
GE870432
GO:0000139
GO:0000271
GO:0001503
GO:0001707
GO:0002062
GO:0003013
GO:0003824
GO:0005515
GO:0005576
GO:0005615
GO:0005783
GO:0005789
GO:0005794
GO:0005975
GO:0006024
GO:0006486
GO:0006487
GO:0006790
GO:0007165
GO:0008217
GO:0008375
GO:0010467
GO:0015012
GO:0015014
GO:0015020
GO:0016020
GO:0016740
GO:0016757
GO:0016758
GO:0023052
GO:0030154
GO:0030210
GO:0036211
GO:0042044
GO:0042311
GO:0042328
GO:0043226
GO:0043541
GO:0044344
GO:0046872
GO:0046982
GO:0048856
GO:0050508
GO:0050509
GO:0050891
GO:0051923
GO:0055065
GO:0055078
GO:0060047
GO:0060350
GO:0070062
GO:1901135
HMNXSV003043488
Hs.100265.0.A1_3p_at
Hs.103682.0.A1_3p_at
Hs.75334.0.S1_3p_a_at
ILMN_1761259
ILMN_2328029
PH_hs_0004312
TC11003446.hg
U67368_s_at
U72263_s_at
g4557572_3p_a_at
Participates
Other forms of this molecule
Modified Residues
Name
Nonsense mutation at L-tyrosine 222
Coordinate
222
PsiMod
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name Identifier Synonyms
hereditary multiple exostoses DOID:206 Osteochondromatosis syndrome (disorder) [Ambiguous], Multiple exostosis syndromes, Multiple congenital exostosis
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