SLC2A9 W23* [plasma membrane]

Stable Identifier
R-HSA-5638203
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
2760230
2760231
2760232
2760234
2760251
2760254
2760255
2760263
2760271
2760287
2760298
2760299
2760301
2760314
2760317
2760322
2760329
56606
63024_at
66229
8099326
A_23_P213014
A_24_P196318
AAF85942
AAH18897
AAI10415
AAL16939
AAY41052
AC005674
AC098976
AC108199
AF210317
AF421859
BC018897
BC110414
CCDS3406
CCDS3407
D6REK5
ENSG00000109667
ENSP00000264784
ENSP00000311383
ENSP00000422209
ENST00000264784
ENST00000309065
ENST00000506583
EntrezGene:56606
g9910553_3p_at
GE82490
GO:0003674
GO:0005215
GO:0005351
GO:0005355
GO:0005575
GO:0005623
GO:0005886
GO:0006810
GO:0008150
GO:0008643
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
HGNC:13446
HPA066229
ILMN_1668312
ILMN_1723803
ILMN_1738406
IPR003663
IPR005828
IPR005829
IPR020846
IPR036259
MIM:606142
MIM:612076
NM_001001290
NM_020041
NP_001001290
NP_064425
PF00083
PH_hs_0005208
PR00171
SLC2A9
SLC2A9-201
SLC2A9-202
SLC2A9-208
uc003gmc.4
uc003gmd.4
uc062vdm.1
UPI000013D56E
UPI000013EE1E
XM_006713968
XM_006713969
XM_011513856
XM_011513857
XM_011513858
XM_011513859
XM_011513860
XM_011513861
XM_011513862
XM_011513865
XM_011513866
XM_011513868
XM_017008457
XM_017008458
XM_017008460
XP_006714031
XP_006714032
XP_011512158
XP_011512159
XP_011512160
XP_011512161
XP_011512162
XP_011512163
XP_011512164
XP_011512167
XP_011512168
XP_011512170
XP_016863946
XP_016863947
XP_016863949
XR_001741290
XR_925341
Participant Of
Other forms of this molecule
Modified Residues
Name
L-tryptophan 23 replaced with unknown
Coordinate
23
PsiMod
A protein modification that effectively removes or replaces an L-tryptophan.
Disease
Name Identifier Synonyms
renal tubular transport disease 447 inborn renal tubular transport disorder
Cross References
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein