ALG11 L86S

Stable Identifier
R-HSA-4570580
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Asparagine-linked glycosylation protein 11 homolog, ALG11_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
ALG11, GT8
Chain
chain:1-492
Reference Transcript
Other Identifiers
00510+2.4.1.131
00513+2.4.1.131
11722486_a_at
11722488_a_at
16774999
3490509
3490515
3490516
3490521
3490522
3490523
3490524
3490525
3490526
3490527
3490528
3490532
3490533
3490534
3490535
3490536
3490537
3490538
3990578
3990587
440138
47214
7969228
A_14_P115902
A_24_P102389
A_33_P3230876
AAH10857
AAH73862
AAI11023
AAI42999
AK296747
AL139082
ALG11
ALG11-202
BAG59331
BC010857
BC073862
BC111022
BC142998
CCDS31977
ENSG00000253710
ENSP00000430236
ENST00000521508
EntrezGene:440138
GO:0003674
GO:0004377
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005783
GO:0005789
GO:0005975
GO:0006464
GO:0006490
GO:0006629
GO:0008150
GO:0009058
GO:0016020
GO:0016021
GO:0016740
GO:0016757
GO:0033577
GO:0043226
GO:0097502
HGNC:32456
HPA047214
ILMN_1660856
IPR001296
IPR031814
MIM:613661
MIM:613666
NM_001004127
NP_001004127
PF00534
PF15924
PH_hs_0040378
TC13001098.hg
uc001vga.4
UPI000044C60E
Participant Of
Other forms of this molecule
Modified Residues
Name
L-leucine 86 replaced with L-serine
Coordinate
86
PsiMod HEY
A protein modification that effectively converts a source amino acid residue to L-serine.
A protein modification that effectively removes or replaces an L-leucine.
Disease
Name Identifier Synonyms
congenital disorder of glycosylation type I 0050570
Cross References
GeneCards
PRO
BRENDA (Homo sapiens)
Orphanet
HMDB Protein