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
00510+2.4.1.259+2.4.1.261
00513+2.4.1.261
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
38575
55503_at
76266_at
7951633
79796
A0A087WTZ3
A0A087WVC0
A0A087WX16
A0A087WZY8
A_24_P795594
AAH09255
AAL25798
AAP97696
AF395532
AF454937
AK025498
AK172828
AL136927
ALG9
ALG9-201
ALG9-210
ALG9-214
ALG9-215
BAB15154
BAD18793
BC009255
CAB66861
CCDS41714
CCDS53709
CCDS73379
CCDS73380
ENSG00000086848
ENSP00000381090
ENSP00000435517
ENSP00000482437
ENSP00000484200
ENST00000398006
ENST00000398006.6
ENST00000531154
ENST00000531154.5
ENST00000614444
ENST00000614444.4
ENST00000616540
ENST00000616540.4
EntrezGene:79796
EntrezGene:ALG9
g13376061_3p_a_at
GE87114
GE87868
GO:0000026
GO:0000030
GO:0003674
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0006464
GO:0006486
GO:0006488
GO:0006629
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0016757
GO:0043226
GO:0052918
GO:0052926
GO:0097502
HGNC:15672
HPA038575
Hs.96918.0.A1_3p_at
ILMN_1732809
IPR005599
IPR039484
MIM:263210
MIM:606941
MIM:608776
NM_001077690
NM_001077691
NM_001077692
NM_001352409
NM_001352410
NM_001352411
NM_001352412
NM_001352413
NM_001352414
NM_001352415
NM_001352416
NM_001352417
NM_001352418
NM_001352419
NM_001352420
NM_001352421
NM_001352422
NM_001352423
NM_024740
NP_001071158
NP_001071159
NP_001071160
NP_001339338
NP_001339339
NP_001339340
NP_001339341
NP_001339342
NP_001339343
NP_001339344
NP_001339345
NP_001339346
NP_001339347
NP_001339348
NP_001339349
NP_001339350
NP_001339351
NP_001339352
NP_079016
NR_147984
PF03901
TC11003493.hg
UPI0000037C0B
UPI000006ED01
UPI000058E4AF
UPI000058E4B0
XM_005277723
XM_006718913
XM_011542992
XM_017018313
XM_017018314
XM_024448695
XP_005277780
XP_006718976
XP_011541294
XP_016873802
XP_016873803
XP_024304463
XR_001747967
XR_001747968
XR_001747969
XR_001747970
XR_001747971
XR_001747972
XR_001747973
XR_001747974
XR_001747975
XR_001747976
XR_001747979
XR_001747980
XR_947863
XR_947864
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