SLC6A18 G79S [plasma membrane]

Stable Identifier
R-HSA-5659751
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:0005328
GO:0005575
GO:0005886
GO:0005887
GO:0006810
GO:0006836
GO:0006865
GO:0008150
GO:0015171
GO:0015293
GO:0016020
GO:0016021
GO:0016324
GO:0022857
GO:0031526
GO:0055085
Hs.213284.0.A1_3p_at
ILMN_1813964
PH_hs_0012330
TC05000017.hg
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 79 replaced with L-serine
Coordinate
79
PsiMod
A protein modification that effectively converts a source amino acid residue to L-serine.
A protein modification that effectively removes or replaces an glycine.
Disease
Name Identifier Synonyms
amino acid metabolic disorder 9252 inborn errors of amino acid metabolism
Cross References
RefSeq
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein
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