Entity Details

Primary name SLC34A3
Entity type gene
Source Source Link

Details

PrimaryID142680
RefseqGeneNG_017008
SymbolSLC34A3
Namesolute carrier family 34 member 3
Chromosome9
Location9q34.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-19
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsNPT2C_HUMAN

GO terms

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GOName
GO:0005436 sodium:phosphate symporter activity
GO:0005886 plasma membrane
GO:0005903 brush border
GO:0006814 sodium ion transport
GO:0006817 phosphate ion transport
GO:0016021 integral component of membrane
GO:0016324 apical plasma membrane
GO:0030643 cellular phosphate ion homeostasis
GO:0031526 brush border membrane
GO:0031982 vesicle
GO:0044341 sodium-dependent phosphate transport

Diseases

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Disease IDSourceNameDescription
241530 OMIMHereditary hypophosphatemic rickets with hypercalciuria (HHRH)Autosomal recessive form of hypophosphatemia characterized by reduced renal phosphate reabsorption and rickets. Increased serum levels of 1,25-dihydroxyvitamin D lead to increase in urinary calcium excretion. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
SLC34A3CLRN1BioGRID, IntAct32296183 details
SLC34A3TMEM234BioGRID, IntAct32296183 details
SLC34A3GPX8BioGRID, IntAct32296183 details
SLC34A3TMEM167BBioGRID, IntAct32296183 details
SLC34A3SNTA1BioGRID, IntAct18468998 details