SLC2A2 R365* [plasma membrane]

Stable Identifier
R-HSA-5638277
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
GLUT2, Solute carrier family 2, facilitated glucose transporter, member 2, Glucose transporter type 2, liver
Icon
SLC2A2 R365* [plasma membrane] icon
SLC2A2 R365* [plasma membrane] icon
Locations in the PathwayBrowser
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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
UniProt:P11168 SLC2A2
Gene Names
SLC2A2, GLUT2
Chain
chain:1-524
Reference Genes
BioGPS Gene:6514 SLC2A2
COSMIC (genes):SLC2A2 SLC2A2
CTD Gene:6514 SLC2A2
dbSNP Gene:6514 SLC2A2
ENSEMBL:ENSG00000163581 SLC2A2
HGNC:11006 SLC2A2
KEGG:hsa:6514 SLC2A2
Monarch:6514 SLC2A2
NCBI Gene:6514 SLC2A2
OMIM:138160 SLC2A2
UCSC:P11168 SLC2A2
Reference Transcript
Other Identifiers
11733276_a_at
11733277_a_at
11733278_at
11748953_a_at
16961485
16961487
206535_PM_at
206535_at
2705213
2705214
2705216
2705217
2705218
2705219
2705221
2705222
2705223
2705224
2705225
2705226
2705227
2705228
2705229
2705232
2705233
2705238
2705240
38238_at
49807_at
6514
8092081
8092083
88058_s_at
A_23_P132569
A_24_P405705
GE58214
GO:0005215
GO:0005353
GO:0005354
GO:0005355
GO:0005737
GO:0005886
GO:0005903
GO:0005911
GO:0005975
GO:0015149
GO:0015755
GO:0015757
GO:0016020
GO:0016324
GO:0022857
GO:0033300
GO:0035774
GO:0046323
GO:0055056
GO:0055085
GO:0070837
GO:1904659
HMNXSV003030325
ILMN_1755720
J03810_at
PH_hs_0010057
TC03001996.hg
TC03001997.hg
g4557850_3p_at
Participates
as a member of
Other forms of this molecule
SLC2A2 R301* [plasma membrane]
SLC2A2 P417L [plasma membrane]
SLC2A2 V423E [plasma membrane]
SLC2A2 Q287* [plasma membrane]
SLC2A2 L46Wfs*29 [plasma membrane]
SLC2A2 L389P [plasma membrane]
SLC2A2 [plasma membrane]
Modified Residues
Name
Nonsense mutation at L-arginine 365
Coordinate
365
PsiMod
L-arginine removal [MOD:01632]
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
renal tubular transport disease DOID:447 inborn renal tubular transport disorder
Cross References
Guide to Pharmacology - Targets
876
ENSEMBL
OpenTargets
HPA
PRO
Pharos - Targets
Orphanet
HMDB Protein
Interactors (1)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q8WWH5 TRUB1      0.527 2
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