Solute carrier family 22 member 15

SLC22A15
Identifiers
Aliases	SLC22A15, FLIPT1, PRO34686, solute carrier family 22 member 15
External IDs	OMIM: 608275; MGI: 3607704; HomoloGene: 41263; GeneCards: SLC22A15; OMA:SLC22A15 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)
End	116,070,054 bp
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)
End	101,924,453 bp
RNA expression pattern
	Top expressed in
	corpus callosum; ; monocyte; ; inferior ganglion of vagus nerve; ; bone marrow; ; C1 segment; ; subthalamic nucleus; ; Brodmann area 46; ; trabecular bone; ; bone marrow cells; ; right lung;
	Top expressed in
	granulocyte; ; spermatid; ; spermatocyte; ; epithelium of lens; ; substantia nigra; ; trigeminal ganglion; ; urethra; ; genital tubercle; ; Paneth cell; ; lip;
	More reference expression data
	n/a
Gene ontology
Molecular function	transmembrane transporter activity; organic anion transmembrane transporter activity;
Cellular component	integral component of membrane; membrane;
Biological process	ion transport; transmembrane transport; organic anion transport;
	Sources:Amigo / QuickGO
Orthologs
	55356
	242126
	ENSG00000163393
	ENSMUSG00000033147
	Q8IZD6
	Q504N2
	NM_018420
	NM_001039371
	NP_060890
	NP_001034460
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene.