SLC17A9

SLC17A9
Identifiers
Aliases	SLC17A9, C20orf59, VNUT, POROK8, solute carrier family 17 member 9
External IDs	OMIM: 612107; MGI: 1919107; HomoloGene: 76562; GeneCards: SLC17A9; OMA:SLC17A9 - orthologs
Gene location (Human)
Chr.	Chromosome 20 (human)
End	62,969,585 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	180,384,073 bp
RNA expression pattern
	Top expressed in
	right lobe of liver; ; stromal cell of endometrium; ; tendon of biceps brachii; ; spleen; ; pylorus; ; bone marrow cells; ; body of stomach; ; pancreatic ductal cell; ; lymph node; ; ascending aorta;
	Top expressed in
	granulocyte; ; large intestine; ; colon; ; molar; ; left colon; ; mesenteric lymph nodes; ; embryo; ; spermatocyte; ; spleen; ; blood;
	More reference expression data
	n/a
Gene ontology
Molecular function	transmembrane transporter activity; transporter activity;
Cellular component	integral component of membrane; membrane;
Biological process	anion transport; transmembrane transport; exocytosis;
	Sources:Amigo / QuickGO
Orthologs
	63910
	228993
	ENSG00000101194
	ENSMUSG00000023393
	Q9BYT1
	Q8VCL5
	NM_001302643; NM_022082
	NM_183161
	NP_001289572; NP_071365
	NP_898984
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene.