Entity Details

Primary name SLC2A9
Entity type gene
Source Source Link

Details

PrimaryID56606
RefseqGeneNG_011540
SymbolSLC2A9
Namesolute carrier family 2 member 9
Chromosome4
Location4p16.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-09-08
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsGTR9_HUMAN

GO terms

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GOName
GO:0005351 carbohydrate:proton symporter activity
GO:0005355 glucose transmembrane transporter activity
GO:0005886 plasma membrane
GO:0008645 hexose transmembrane transport
GO:0015143 urate transmembrane transporter activity
GO:0015747 urate transport
GO:0015755 fructose transmembrane transport
GO:0016021 integral component of membrane
GO:0016323 basolateral plasma membrane
GO:0016324 apical plasma membrane
GO:0046415 urate metabolic process
GO:1904659 glucose transmembrane transport

Diseases

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Disease IDSourceNameDescription
612076 OMIMHypouricemia renal 2 (RHUC2)A disorder characterized by impaired uric acid reabsorption at the apical membrane of proximal renal tubule cells, and high urinary urate excretion. Patients often appear asymptomatic, but may be subject to exercise-induced acute renal failure, chronic renal dysfunction and nephrolithiasis. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
SLC2A9ITM2BUniProt31695625 details
SLC2A9EMC4UniProt31695625 details
SLC2A9TKTBioGRID26344197 details