SLC2A9 R198C [plasma membrane]

Stable Identifier
R-HSA-5638232
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
GLUT9, Solute carrier family 2, facilitated glucose transporter member 9, GTR9_HUMAN
Locations in the PathwayBrowser
External Reference Information
External Reference
Gene Names
SLC2A9, GLUT9
Chain
chain:1-540
Other Identifiers
0003800113
11734177_a_at
16974250
219991_at
2760229
2760230
2760231
2760232
2760234
2760251
2760254
2760255
2760263
2760271
2760287
2760298
2760299
2760301
2760314
2760317
2760322
2760329
2760330
56606
63024_at
8099326
A_23_P213014
A_24_P196318
GE82490
GO:0003674
GO:0005351
GO:0005355
GO:0005575
GO:0005886
GO:0006810
GO:0008150
GO:0008645
GO:0015143
GO:0015747
GO:0016020
GO:0016021
GO:0016323
GO:0016324
GO:0022857
GO:0034641
GO:0044281
GO:0046415
GO:0055085
GO:1902600
GO:1904659
ILMN_1668312
ILMN_1723803
ILMN_1738406
PH_hs_0005208
g9910553_3p_at
Participant Of
Other forms of this molecule
Modified Residues
Name
L-arginine 198 replaced with L-cysteine
Coordinate
198
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-cysteine.
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
renal tubular transport disease 447 inborn renal tubular transport disorder
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