SLC22A9

Protein-coding gene in the species Homo sapiens
SLC22A9
Identifiers
AliasesSLC22A9, HOAT4, OAT4, OAT7, UST3H, ust3, solute carrier family 22 member 9
External IDsOMIM: 607579; MGI: 3042283; HomoloGene: 137850; GeneCards: SLC22A9; OMA:SLC22A9 - orthologs
Gene location (Human)
Chromosome 11 (human)
Chr.Chromosome 11 (human)[1]
Chromosome 11 (human)
Genomic location for SLC22A9
Genomic location for SLC22A9
Band11q12.3Start63,369,785 bp[1]
End63,410,294 bp[1]
Gene location (Mouse)
Chromosome 19 (mouse)
Chr.Chromosome 19 (mouse)[2]
Chromosome 19 (mouse)
Genomic location for SLC22A9
Genomic location for SLC22A9
Band19|19 AStart7,841,753 bp[2]
End7,943,392 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • Brodmann area 9

  • gallbladder

  • prefrontal cortex

  • amygdala

  • islet of Langerhans

  • superior frontal gyrus

  • lymph node

  • putamen

  • hippocampal formation
Top expressed in
  • proximal tubule

  • liver

  • metanephros

  • 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
SpeciesHumanMouse
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 MbChr 19: 7.84 – 7.94 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000149742 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000067656 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ 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.
  6. ^ 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.
  7. ^ "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. Bibcode:2002PNAS...9916899M. 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. S2CID 348962.
  • 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.

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By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
  • Na+/Ca2+ exchanger
(9):
(10):
SLC11–20
(11):
(12):
(13):
(14):
(15):
(16):
(17):
(18):
(19):
(20):
SLC21–30
(21):
(22):
(23):
  • Na+-dependent ascorbic acid transporter
(24):
  • Na+/(Ca2+-K+) exchanger
(25):
(26):
(27):
(28):
(29):
(30):
SLC31–40
(31):
(32):
(33):
(34):
(35):
(36):
(37):
(38):
(39):
(40):
  • basolateral iron transporter
SLC41–48
(41):
(42):
(43):
  • Na+-independent, system-L like amino-acid transporter
(44):
(45):
(46):
(47):
(48):
SLCO1–4
Symporter, Cotransporter
  • Na+/K+,Cl
  • Na+/Pi3
  • Na+/Cl
  • Na+/glucose
  • Na+/I
  • Cl/K+
Antiporter (exchanger)
  • Na+/H+
  • Na+/Ca2+
    • Na+/(Ca2+-K+) - Cl/HCO
      3
      (Band 3)
  • Cl-formate
  • Cl-oxalate
see also solute carrier disorders


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