Monocarboxylate transporter 9

SLC16A9
Identifiers
Aliases	SLC16A9, C10orf36, MCT9, solute carrier family 16 member 9
External IDs	OMIM: 614242; MGI: 1914109; HomoloGene: 32642; GeneCards: SLC16A9; OMA:SLC16A9 - orthologs
Gene location (Human)
Chr.	Chromosome 10 (human)
End	59,736,002 bp
Gene location (Mouse)
Chr.	Chromosome 10 (mouse)
End	70,121,798 bp
RNA expression pattern
	Top expressed in
	left adrenal cortex; ; right adrenal cortex; ; nasal epithelium; ; mucosa of colon; ; mucosa of sigmoid colon; ; mucosa of ileum; ; human kidney; ; gums; ; gingival epithelium; ; ventricular zone;
	Top expressed in
	retinal pigment epithelium; ; meninges; ; right lung; ; human kidney; ; right kidney; ; right lung lobe; ; proximal tubule; ; ciliary body; ; lumbar spinal ganglion; ; aortic valve;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding; symporter activity; monocarboxylic acid transmembrane transporter activity;
Cellular component	plasma membrane; membrane; integral component of membrane; integral component of plasma membrane;
Biological process	urate metabolic process; transmembrane transport; monocarboxylic acid transport;
	Sources:Amigo / QuickGO
Orthologs
	220963
	66859
	ENSG00000165449
	ENSMUSG00000037762
	Q7RTY1
	Q7TM99
NM_194298; NM_001323977; NM_001323978; NM_001323979; NM_001323980;
	NM_001323981
	NM_025807
NP_001310906; NP_001310907; NP_001310908; NP_001310909; NP_001310910;
	NP_919274
	NP_080083
	Wikidata
View/Edit Human	View/Edit Mouse

Monocarboxylate transporter 9 (MCT9, solute carrier family 16, member 9, SLC16A9) is a protein that in humans is encoded by the SLC16A9 gene.^[5]