SLC2A2 L389P [plasma membrane]

Stable Identifier
R-HSA-5638294
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
GLUT2, Solute carrier family 2, facilitated glucose transporter, member 2, Glucose transporter type 2, liver
SLC2A2 L389P [plasma membrane] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
1562197 Mammalian facilitative glucose transporter family: structure and molecular regulation.

Pessin, JE, Bell, GI

Annu Rev Physiol 1992
External Reference Information
External Reference
Gene Names
SLC2A2, GLUT2
Chain
chain:1-524
Other Identifiers
0002350551
10444
11733276_a_at
11733277_a_at
11733278_at
11748953_a_at
16961487
206535_at
2705218
2705219
2705221
2705222
2705223
2705225
2705226
2705227
2705229
2705232
2705233
2705238
2705240
28997
28998
6514
8092083
A0A0C4DH64
A_23_P132569
A_24_P405705
AAA59514
AC061708
AC092918
AK290846
AK298418
AK313622
BAF83535
BAG36383
BAH12783
C9J0E8
CAB010444
CCDS3215
CH471052
EAW78499
ENSG00000163581
ENSP00000323568
ENST00000314251
EntrezGene:6514
F8WBJ2
g4557850_3p_at
GE58214
GO:0003674
GO:0005215
GO:0005355
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005886
GO:0005887
GO:0005903
GO:0005911
GO:0005975
GO:0006810
GO:0007267
GO:0008150
GO:0008643
GO:0008645
GO:0015149
GO:0016020
GO:0016021
GO:0016324
GO:0022857
GO:0033300
GO:0050796
GO:0055056
GO:0055085
GO:0070837
GO:0106001
GO:1904659
HGNC:11006
HPA028997
HPA028998
ILMN_1755720
IPR002440
IPR003663
IPR005828
IPR005829
IPR020846
IPR036259
J03810
J03810_at
MIM:125853
MIM:138160
MIM:227810
NM_000340
NM_001278658
NM_001278659
NP_000331
NP_001265587
NP_001265588
PF00083
PH_hs_0010057
PR00171
PR01191
SLC2A2
SLC2A2-201
TC03001997.hg
uc003fhe.2
UPI000004EC97
XM_011513087
XM_011513089
XP_011511389
Participant Of
Other forms of this molecule
Modified Residues
Name
L-leucine 389 replaced with L-proline
Coordinate
389
PsiMod
A protein modification that effectively converts a source amino acid residue to L-proline.
A protein modification that effectively removes or replaces an L-leucine.
Disease
Name Identifier Synonyms
renal tubular transport disease 447 inborn renal tubular transport disorder
Cross References
OpenTargets
GeneCards
PRO
Orphanet
HMDB Protein