SLC22A9

Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene.^[5][6][7]

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)[1] Band 11q12.3 Start 63,369,785 bp[1] End 63,410,294 bp[1]
Gene location (Mouse) Chr. Chromosome 19 (mouse)[2] Band 19|19 A Start 7,841,753 bp[2] End 7,943,392 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) 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 BioGPS 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 Species Human Mouse Entrez 114571 171405 Ensembl ENSG00000149742 ENSMUSG00000067656 UniProt Q8IVM8 Q76M72 RefSeq (mRNA) NM_080866 NM_134256 NM_001361980 RefSeq (protein) NP_543142 NP_599017 NP_001348909 Location (UCSC) Chr 11: 63.37 – 63.41 Mb Chr 19: 7.84 – 7.94 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

See also

• SLC22A9+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)