SLC6A18 G79S

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
11885
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
AAH56757
AC114291
AK055798
BAB71018
BC056757
CCDS3860
ENSG00000164363
ENSP00000323549
ENST00000324642
EntrezGene:348932
GO:0003333
GO:0003674
GO:0005215
GO:0005328
GO:0005575
GO:0005623
GO:0005886
GO:0005887
GO:0006810
GO:0006836
GO:0006865
GO:0008150
GO:0015171
GO:0015175
GO:0015293
GO:0015804
GO:0016020
GO:0016021
GO:0022857
GO:0031526
GO:0055085
HGNC:26441
HPA011885
Hs.213284.0.A1_3p_at
ILMN_1813964
IPR000175
IPR002438
IPR037272
MIM:610300
NM_182632
NP_872438
PF00209
PH_hs_0012330
PR00176
PR01206
SLC6A18
SLC6A18-201
TC05000017.hg
uc003jby.2
UPI0000197EA2
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 79 replaced with L-serine
Coordinate
79
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 glycine.
Disease
Name Identifier Synonyms
amino acid metabolic disorder 9252 inborn errors of amino acid metabolism
Cross References
RefSeq
GeneCards
PRO
Orphanet
HMDB Protein