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.