SLC2A10 W170* [plasma membrane]

Stable Identifier
R-HSA-5632790
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
GLUT10, Solute carrier family 2, facilitated glucose transporter member 10, GTR10_HUMAN
Locations in the PathwayBrowser
Expand all
External Reference Information
External Reference
UniProt:O95528 SLC2A10
Gene Names
SLC2A10, GLUT10
Chain
chain:1-541
Reference Genes
BioGPS Gene:81031 SLC2A10
COSMIC (genes):SLC2A10 SLC2A10
CTD Gene:81031 SLC2A10
dbSNP Gene:81031 SLC2A10
ENSEMBL:ENSG00000197496 SLC2A10
HGNC:13444 SLC2A10
KEGG Gene (Homo sapiens):81031 SLC2A10
Monarch:81031 SLC2A10
NCBI Gene:81031 SLC2A10
OMIM:606145 SLC2A10
UCSC:O95528 SLC2A10
Reference Transcript
Other Identifiers
0000510301
11744516_a_at
11744517_a_at
11744518_a_at
16914469
221024_s_at
3887455
3887456
3887464
3887465
3887466
3887467
3887468
3887469
3887470
3887471
3887472
3887473
41015
48553_at
48554_at
8063177
81031
A_23_P210521
A_24_P271323
AAI01658
AAI13424
AAK26294
AAK31911
AF248053
AF321240
AK290961
AL031055
AL137188
BAF83650
BC101657
BC113423
CAB69822
CCDS13402
CH471077
EAW75724
ENSG00000197496
ENSP00000352216
ENST00000359271
ENST00000359271.3
EntrezGene:81031
EntrezGene:SLC2A10
g13540546_3p_s_at
GE62735
GO:0003674
GO:0005215
GO:0005351
GO:0005575
GO:0005622
GO:0005623
GO:0005737
GO:0005886
GO:0005887
GO:0006810
GO:0008150
GO:0008643
GO:0008645
GO:0012505
GO:0016020
GO:0016021
GO:0022857
GO:0046323
GO:0048471
GO:0055085
GO:1902600
GO:1904659
HGNC:13444
HPA041015
ILMN_1663351
ILMN_2120247
IPR003663
IPR005828
IPR005829
IPR020846
IPR036259
MIM:208050
MIM:606145
NM_030777
NP_110404
PF00083
PH_hs_0015715
PR00171
SLC2A10
SLC2A10-201
TC20000366.hg
TC20001244.hg
UPI000012BC8D
XM_011529060
XM_011529061
XM_017028087
XP_011527362
XP_011527363
XP_016883576
Participant Of
hasMember
Other forms of this molecule
SLC2A10 [plasma membrane]
SLC2A10 G445Efs*40 [plasma membrane]
SLC2A10 V321Cfs*71 [plasma membrane]
SLC2A10 G426W [plasma membrane]
SLC2A10 S81R [plasma membrane]
SLC2A10 R132W [plasma membrane]
Modified Residues
Name
L-tryptophan 170 replaced with unknown
Coordinate
170
PsiMod
L-tryptophan removal [MOD:01648]
A protein modification that effectively removes or replaces an L-tryptophan.
Disease
Name Identifier Synonyms
arterial tortuosity syndrome 0050645
Cross References
RefSeq
OpenTargets
GeneCards
HPA
Ensembl
PRO
Orphanet
HMDB Protein
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