SLC2A9 G216R [plasma membrane]

Stable Identifier
R-HSA-5638184
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
XM_024454150
XM_024454151
XM_024454152
XM_024454153
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
XP_024309918
XP_024309919
XP_024309920
XP_024309921
XR_001741290
XR_925341
Participant Of
Other forms of this molecule
Modified Residues
Name
glycine 216 replaced with L-arginine
Coordinate
216
PsiMod
A protein modification that effectively converts a source amino acid residue to an L-arginine.
A protein modification that effectively removes or replaces an glycine.
Disease
Name Identifier Synonyms
renal tubular transport disease 447 inborn renal tubular transport disorder
Cross References
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein