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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
Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective SLC2A10 causes arterial tortuosity syndrome (ATS) (Homo sapiens)
Defective SLC2A10 does not transport Glc from extracellular region to cytosol (Homo sapiens)
SLC2A10 mutants [plasma membrane] (Homo sapiens)
SLC2A10 W170* [plasma membrane] (Homo sapiens)
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
ENSEMBL_homo_sapiens_GENE: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
RefSeq:NM_030777.3 SLC2A10
Other Identifiers
0000510301
11744516_a_at
11744517_a_at
11744518_a_at
16914469
221024_s_at
3887454
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
EntrezGene:81031
g13540546_3p_s_at
GE62735
GO:0003674
GO:0005215
GO:0005351
GO:0005355
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:0048471
GO:0055056
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
uc002xsl.4
UPI000012BC8D
XM_011529060
XM_011529061
XM_017028087
XP_011527362
XP_011527363
XP_016883576
Participant Of
hasMember
SLC2A10 mutants [plasma membrane]
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
NP_110404.1
OpenTargets
ENSG00000197496
GeneCards
O95528
PRO
O95528
Orphanet
15318
HMDB Protein
HMDBP11760
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