Anion exchange transporter

SLC26A7
Identifiers
Aliases	SLC26A7, SUT2, solute carrier family 26 member 7
External IDs	OMIM: 608479; MGI: 2384791; HomoloGene: 13770; GeneCards: SLC26A7; OMA:SLC26A7 - orthologs
Gene location (Human)
Chr.	Chromosome 8 (human)
End	91,398,155 bp
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)
End	14,621,805 bp
RNA expression pattern
	Top expressed in
	thyroid gland; ; right lobe of thyroid gland; ; left lobe of thyroid gland; ; retinal pigment epithelium; ; renal medulla; ; human kidney; ; testicle; ; endometrium; ; lymph node; ; placenta;
	Top expressed in
	vestibular membrane of cochlear duct; ; retinal pigment epithelium; ; ciliary body; ; iris; ; olfactory epithelium; ; renal corpuscle; ; vestibular sensory epithelium; ; pineal gland; ; lumbar spinal ganglion; ; molar;
	More reference expression data
	n/a
Gene ontology
Molecular function	anion channel activity; anion transmembrane transporter activity; sulfate transmembrane transporter activity; secondary active sulfate transmembrane transporter activity; bicarbonate transmembrane transporter activity; oxalate transmembrane transporter activity; chloride channel activity; chloride transmembrane transporter activity;
Cellular component	cytoplasm; integral component of membrane; endosome; membrane; plasma membrane; integral component of plasma membrane; recycling endosome membrane; basolateral plasma membrane;
Biological process	oxalate transport; sulfate transport; gastric acid secretion; regulation of membrane potential; regulation of intracellular pH; ion transport; anion transport; bicarbonate transport; chloride transport; chloride transmembrane transport; anion transmembrane transport; sulfate transmembrane transport; transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	115111
	208890
	ENSG00000147606
	ENSMUSG00000040569
	Q8TE54
	Q8R2Z3
	NM_134266; NM_001282356; NM_001282357; NM_052832
	NM_145947
	NP_001269285; NP_001269286; NP_439897; NP_599028
	NP_666059
	Wikidata
View/Edit Human	View/Edit Mouse

Anion exchange transporter is a protein that in humans is encoded by the SLC26A7 gene.^[5]^[6]^[7]^[8]

Function

This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in their genomic (number and size of exons) and protein (aa length among species) structures yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Splice variants that use both alternate transcription initiation and polyadenylation sites have been described for this gene.^[8]

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Anion exchange transporter

Contents

Function

See also

References

Further reading