Entity Details

Primary name SLC26A3
Entity type gene
Source Source Link

Details

PrimaryID1811
RefseqGeneNG_008046
SymbolSLC26A3
Namesolute carrier family 26 member 3
Chromosome7
Location7q22.3-q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-01-09
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsS26A3_HUMAN

GO terms

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GOName
GO:0005215 transporter activity
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0006811 ion transport
GO:0006820 anion transport
GO:0007588 excretion
GO:0008271 secondary active sulfate transmembrane transporter activity
GO:0015106 bicarbonate transmembrane transporter activity
GO:0015108 chloride transmembrane transporter activity
GO:0015116 sulfate transmembrane transporter activity
GO:0015301 anion:anion antiporter activity
GO:0016020 membrane
GO:0016324 apical plasma membrane
GO:0019531 oxalate transmembrane transporter activity
GO:0031526 brush border membrane
GO:0048240 sperm capacitation
GO:0051454 intracellular pH elevation
GO:0060081 membrane hyperpolarization
GO:0071320 cellular response to cAMP
GO:0097225 sperm midpiece

Diseases

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Disease IDSourceNameDescription
214700 OMIMDiarrhea 1, secretory chloride, congenital (DIAR1)A disease characterized by voluminous watery stools containing an excess of chloride. The children with this disease are often premature. The disease is caused by variants affecting the gene represented in this entry.

Interactions

2 interactions

InteractorPartnerSourcesPublicationsLink
SLC26A3SLC9A3R2BioGRID, MINT12369822 details
SLC26A3SLC9A3R1HPRD12369822 details