SLC6A18 G496R [plasma membrane]

Stable Identifier
R-HSA-5659726
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
Sodium- and chloride-dependent transporter XTRP2
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC6A18, XTRP2
Chain
chain:1-628
Reference Transcript
Other Identifiers
0000070441
11732930_a_at
16982717
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:0003333
GO:0003674
GO:0005575
GO:0005886
GO:0005887
GO:0006810
GO:0006836
GO:0006865
GO:0008150
GO:0015293
GO:0016020
GO:0016021
GO:0016324
GO:0022857
GO:0031526
GO:0035725
GO:0055085
GO:1905039
HMNXSV003041959
Hs.213284.0.A1_3p_at
ILMN_1813964
PH_hs_0012330
TC05000017.hg
Participates
Other forms of this molecule
Modified Residues
Name
glycine 496 replaced with L-arginine
Coordinate
496
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
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
GeneCards
PRO
Pharos - Targets
Orphanet
GlyGen
HMDB Protein
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