SLC22A13

SLC22A13
Identifiers
Aliases	SLC22A13, OAT10, OCTL1, OCTL3, ORCTL-3, ORCTL3, solute carrier family 22 member 13
External IDs	OMIM: 604047; MGI: 2143107; HomoloGene: 3140; GeneCards: SLC22A13; OMA:SLC22A13 - orthologs
Gene location (Human)
Chr.	Chromosome 3 (human)
End	38,278,757 bp
Gene location (Mouse)
Chr.	Chromosome 9 (mouse)
End	119,038,164 bp
RNA expression pattern
	Top expressed in
	renal cortex; ; stromal cell of endometrium; ; metanephros; ; human kidney; ; apex of heart; ; muscle of thigh; ; blood; ; mucosa of transverse colon; ; Cerebellum; ; cerebellar cortex;
	Top expressed in
	right kidney; ; human kidney; ; proximal tubule; ; proximal straight tubule; ; morula; ; ganglion of vagus nerve; ; thyroid gland; ; embryo; ; convoluted tubule; ; blastocyst;
	More reference expression data
	n/a
Gene ontology
Molecular function	transmembrane transporter activity; organic cation transmembrane transporter activity; nicotinate transmembrane transporter activity; inorganic anion exchanger activity; sodium-independent organic anion transmembrane transporter activity;
Cellular component	integral component of plasma membrane; apical plasma membrane; membrane; extracellular exosome; integral component of membrane; plasma membrane;
Biological process	nicotinate transport; transmembrane transport; urate transport; organic cation transport; NAD biosynthesis via nicotinamide riboside salvage pathway; inorganic anion transport; sodium-independent organic anion transport;
	Sources:Amigo / QuickGO
Orthologs
	9390
	102570
	ENSG00000172940
	ENSMUSG00000074028
	Q9Y226
	Q6A4L0
	NM_004256
	NM_133980
	NP_004247
	NP_598741
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 22 member 13 is a protein that in humans is encoded by the SLC22A13 gene.