SLC2A9 T125M [plasma membrane]

Stable Identifier
R-HSA-5638188
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
11734177_a_at
16974250
219991_PM_at
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:0005215
GO:0005351
GO:0005353
GO:0005355
GO:0005515
GO:0005886
GO:0008645
GO:0015143
GO:0015149
GO:0015747
GO:0015749
GO:0015755
GO:0016020
GO:0016323
GO:0016324
GO:0022857
GO:0046415
GO:0055085
GO:1902600
GO:1904659
HMNXSV003004503
HMNXSV003030607
ILMN_1668312
ILMN_1723803
ILMN_1738406
PH_hs_0005208
g9910553_3p_at
Participates
Other forms of this molecule
Modified Residues
Name
L-threonine 125 replaced with L-methionine
Coordinate
125
PsiMod
A protein modification that effectively converts a source amino acid residue to L-methionine.
A protein modification that effectively removes or replaces an L-threonine.
Disease
Name Identifier Synonyms
renal tubular transport disease DOID:447 inborn renal tubular transport disorder
Cross References
Guide to Pharmacology - Targets
882
OpenTargets
GeneCards
PRO
Pharos - Targets
Orphanet
HMDB Protein
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