SLC22A9

Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene.[3][4][5]

SLC22A9
Identifiers
Aliases	SLC22A9, HOAT4, OAT4, OAT7, UST3H, ust3, solute carrier family 22 member 9
External IDs	OMIM: 607579 HomoloGene: 137850 GeneCards: SLC22A9
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11q12.3 Start 63,369,785 bp[1] End 63,410,294 bp[1]
Gene ontology Molecular function • sodium-independent organic anion transmembrane transporter activity • short-chain fatty acid uptake transporter activity • anion:anion antiporter activity • inorganic anion exchanger activity • urate transmembrane transporter activity Cellular component • integral component of membrane • cell 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	n/a
Ensembl	ENSG00000149742	n/a
UniProt	Q8IVM8	n/a
RefSeq (mRNA)	NM_080866	n/a
RefSeq (protein)	NP_543142	n/a
Location (UCSC)	Chr 11: 63.37 – 63.41 Mb	n/a
PubMed search	[2]	n/a
Wikidata
View/Edit Human

See also

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

References

1. GRCh38: Ensembl release 89: ENSG00000149742 - Ensembl, May 2017
2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
3. Sun W, Wu RR, van Poelje PD, Erion MD (Apr 2001). "Isolation of a family of organic anion transporters from human liver and kidney". Biochem Biophys Res Commun. 283 (2): 417–22. doi:10.1006/bbrc.2001.4774. PMID 11327718.
4. Shin HJ, Anzai N, Enomoto A, He X, Kim do K, Endou H, Kanai Y (Apr 2007). "Novel liver-specific organic anion transporter OAT7 that operates the exchange of sulfate conjugates for short chain fatty acid butyrate". Hepatology. 45 (4): 1046–55. doi:10.1002/hep.21596. PMID 17393504. S2CID 42571618.
5. "Entrez Gene: SLC22A9 solute carrier family 22 (organic anion/cation transporter), member 9".

Further reading

• Zhou F, Hong M, You G (2007). "Regulation of human organic anion transporter 4 by progesterone and protein kinase C in human placental BeWo cells". Am. J. Physiol. Endocrinol. Metab. 293 (1): E57–61. doi:10.1152/ajpendo.00696.2006. PMID 17341544.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Ekaratanawong S, Anzai N, Jutabha P, et al. (2005). "Human organic anion transporter 4 is a renal apical organic anion/dicarboxylate exchanger in the proximal tubules". J. Pharmacol. Sci. 94 (3): 297–304. doi:10.1254/jphs.94.297. PMID 15037815.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Ugele B, St-Pierre MV, Pihusch M, et al. (2003). "Characterization and identification of steroid sulfate transporters of human placenta". Am. J. Physiol. Endocrinol. Metab. 284 (2): E390–8. doi:10.1152/ajpendo.00257.2002. PMID 12409283.
• Cha SH, Sekine T, Kusuhara H, et al. (2000). "Molecular cloning and characterization of multispecific organic anion transporter 4 expressed in the placenta". J. Biol. Chem. 275 (6): 4507–12. doi:10.1074/jbc.275.6.4507. PMID 10660625.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.