SLC22A11

SLC22A11
Identifiers
Aliases	SLC22A11, OAT4, hOAT4, solute carrier family 22 member 11
External IDs	OMIM: 607097; HomoloGene: 81863; GeneCards: SLC22A11; OMA:SLC22A11 - orthologs
Gene location (Human)
Chr.	Chromosome 11 (human)
End	64,572,875 bp
RNA expression pattern
	Top expressed in
	placenta; ; kidney tubule; ; metanephric glomerulus; ; human kidney; ; testicle; ; corpus epididymis; ; caput epididymis; ; tail of epididymis; ; renal medulla; ; right adrenal cortex;
	n/a
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	organic anion transmembrane transporter activity; protein binding; inorganic anion exchanger activity; transmembrane transporter activity; sodium-independent organic anion transmembrane transporter activity; urate transmembrane transporter activity;
Cellular component	integral component of membrane; plasma membrane; integral component of plasma membrane; extracellular exosome; apical plasma membrane; external side of plasma membrane; membrane;
Biological process	sodium-independent organic anion transport; ion transport; urate metabolic process; organic anion transport; transmembrane transport; inorganic anion transport; urate transport; organic acid transmembrane transport; transport;
	Sources:Amigo / QuickGO
Orthologs
	55867
	n/a
	ENSG00000168065
	n/a
	Q9NSA0
	n/a
	NM_001307985; NM_018484
	n/a
	NP_001294914; NP_060954
	n/a
	Wikidata
View/Edit Human

Solute carrier family 22 member 11 is a protein that in humans is encoded by the SLC22A11 gene.

The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus.