SLC6A18 G79S [plasma membrane]

Stable Identifier
R-HSA-5659751
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
Sodium- and chloride-dependent transporter XTRP2
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:Q96N87 SLC6A18
Gene Names
SLC6A18, B0AT3, XTRP2
Chain
chain:1-628
Reference Genes
BioGPS Gene:348932 SLC6A18
COSMIC (genes):SLC6A18 SLC6A18
CTD Gene:348932 SLC6A18
dbSNP Gene:348932 SLC6A18
ENSEMBL:ENSG00000164363 SLC6A18
ENSEMBL_homo_sapiens_GENE:ENSG00000164363.10 SLC6A18
HGNC:26441 SLC6A18
KEGG Gene (Homo sapiens):348932 SLC6A18
Monarch:348932 SLC6A18
NCBI Gene:348932 SLC6A18
OMIM:610300 SLC6A18
UCSC:Q96N87 SLC6A18
Reference Transcript
Other Identifiers
11732930_a_at
16982717
238215_PM_at
238215_at
2799057
2799058
2799059
2799065
2799066
2799067
2799068
2799069
2799070
2799071
2799073
2799075
2799076
2799078
2799079
2799081
2799082
2799084
2799085
2799086
348932
71308_at
8104281
A_24_P212234
GO:0003014
GO:0003333
GO:0005215
GO:0005886
GO:0006836
GO:0006865
GO:0015171
GO:0015293
GO:0015804
GO:0016020
GO:0016324
GO:0022857
GO:0031526
GO:0035725
GO:0055085
GO:0071702
GO:0071705
GO:0140931
GO:1990297
HMNXSV003041959
Hs.213284.0.A1_3p_at
ILMN_1813964
PH_hs_0012330
TC05000017.hg
Participates
as a member of
Other forms of this molecule
SLC6A18 G496R [plasma membrane]
SLC6A18 [plasma membrane]
Modified Residues
Name
glycine 79 replaced with L-serine
Coordinate
79
PsiMod
glycine removal [MOD:01638]
A protein modification that effectively removes or replaces an glycine.
L-serine residue [MOD:00025]
A protein modification that effectively converts a source amino acid residue to L-serine.
Disease
Name Identifier Synonyms
amino acid metabolic disorder DOID:9252 inborn errors of amino acid metabolism
Cross References
RefSeq
Guide to Pharmacology - Targets
941
OpenTargets
HPA
GeneCards
Ensembl
PRO
Pharos - Targets
Orphanet
HMDB Protein
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