SLC22A9

SLC22A9
Identifiers
Aliases	SLC22A9, HOAT4, OAT4, OAT7, UST3H, ust3, solute carrier family 22 member 9
External IDs	OMIM: 607579; MGI: 3042283; HomoloGene: 137850; GeneCards: SLC22A9; OMA:SLC22A9 - orthologs
Gene location (Human)
Chr.	Chromosome 11 (human)
End	63,410,294 bp
Gene location (Mouse)
Chr.	Chromosome 19 (mouse)
End	7,943,392 bp
RNA expression pattern
	Top expressed in
	right lobe of liver; ; Brodmann area 9; ; right frontal lobe; ; skin of thigh; ; anterior cingulate cortex; ; gallbladder; ; prefrontal cortex; ; primary visual cortex; ; Amygdala; ; islet of Langerhans;
	Top expressed in
	proximal tubule; ; liver; ; right kidney; ; metanephros; ; human kidney;
	More reference expression data
	n/a
Gene ontology
Molecular function	sodium-independent organic anion transmembrane transporter activity; short-chain fatty acid transmembrane transporter activity; inorganic anion exchanger activity; urate transmembrane transporter activity;
Cellular component	integral component of membrane; plasma membrane; basolateral plasma membrane; integral component of plasma membrane; membrane;
Biological process	sodium-independent organic anion transport; hormone transport; short-chain fatty acid import; transmembrane transport; anion transmembrane transport; inorganic anion transport; urate transport; organic anion transport;
	Sources:Amigo / QuickGO
Orthologs
	114571
	171405
	ENSG00000149742
	ENSMUSG00000067656
	Q8IVM8
	Q76M72
	NM_080866
	NM_134256; NM_001361980
	NP_543142
	NP_599017; NP_001348909
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene.