SLC2A9 W23* [plasma membrane]

Stable Identifier
R-HSA-5638203
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
plasma membrane
Synonyms
GLUT9, Solute carrier family 2, facilitated glucose transporter member 9, GTR9_HUMAN
Locations in the PathwayBrowser
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External Reference Information
External Reference
UniProt:Q9NRM0 SLC2A9
Gene Names
SLC2A9, GLUT9
Chain
chain:1-540
Reference Genes
BioGPS Gene:56606 SLC2A9
COSMIC - genes:SLC2A9 SLC2A9
CTD Gene:56606 SLC2A9
dbSNP Gene:56606 SLC2A9
ENSEMBL:ENSG00000109667 SLC2A9
HGNC:13446 SLC2A9
KEGG:hsa:56606 SLC2A9
Monarch:56606 SLC2A9
NCBI Gene:56606 SLC2A9
OMIM:606142 SLC2A9
UCSC:Q9NRM0 SLC2A9
Reference Transcript
Participates
as a member of
Other forms of this molecule
SLC2A9 [plasma membrane]
SLC2A9 R380W [plasma membrane]
SLC2A9 L75R [plasma membrane]
SLC2A9 T125M [plasma membrane]
SLC2A9 G216R [plasma membrane]
SLC2A9 R198C [plasma membrane]
SLC2A9 R171C [plasma membrane]
Modified Residues
Name
Nonsense mutation at L-tryptophan 23
Coordinate
23
PsiMod
L-tryptophan removal [MOD:01648]
A protein modification that effectively removes or replaces an L-tryptophan.
Disease
Name Identifier Synonyms
renal tubular transport disease DOID:447 inborn renal tubular transport disorder
Cross References
RefSeq
Guide to Pharmacology - Targets
882
OpenTargets
ENSEMBL
Mondo
PRO
GlyGen
PDB
HPA
GeneCards
Pharos - Targets
Orphanet
HMDB Protein
Interactors (3)
Accession #Entities Entities Confidence Score Evidence (IntAct)
 UniProt:Q9UI26 IPO11      0.527 2
 UniProt:Q9Y6D6 BIG1      0.527 2
 UniProt:Q5VYK3 ECM29      0.527 2
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