ALG9 E523K [endoplasmic reticulum membrane]

Stable Identifier
R-HSA-4720482
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Alpha-1,2-mannosyltransferase ALG9, ALG9_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ALG9, DIBD1
Chain
chain:1-611
Other Identifiers
0006290025
11726400_a_at
11726401_a_at
11726402_s_at
11747122_x_at
16744322
219374_s_at
228817_at
3391086
3391090
3391092
3391094
3391095
3391096
3391097
3391098
3391104
3391105
3391113
3391114
3391115
3391116
3391117
3391120
3391121
3391124
3391126
3391127
3391130
3391131
3391132
3391133
3391134
3391135
3391136
3391137
55503_at
76266_at
7951633
79796
A_24_P795594
GE87114
GE87868
GO:0000026
GO:0000030
GO:0003674
GO:0005575
GO:0005622
GO:0005737
GO:0005783
GO:0005789
GO:0006464
GO:0006486
GO:0006487
GO:0006488
GO:0006629
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0016757
GO:0043226
GO:0052918
GO:0052926
GO:0097502
Hs.96918.0.A1_3p_at
ILMN_1732809
TC11003493.hg
g13376061_3p_a_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-glutamic acid 523 replaced with L-lysine
Coordinate
523
PsiMod
A protein modification that effectively removes or replaces an L-glutamic acid.
A protein modification that effectively converts a source amino acid residue to L-lysine.
Disease
Name Identifier Synonyms
congenital disorder of glycosylation type I 0050570
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