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SLC22A9

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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)
Chromosome 11 (human)Genomic location for SLC22A9Genomic location for SLC22A9
Band11q12.3Start63,369,785 bp
End63,410,294 bp
Gene location (Mouse)
Chromosome 19 (mouse)
Chr.Chromosome 19 (mouse)
Chromosome 19 (mouse)Genomic location for SLC22A9Genomic location for SLC22A9
Band19|19 AStart7,841,753 bp
End7,943,392 bp
RNA expression pattern
Bgee
HumanMouse (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
Cellular component
Biological process
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
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene.

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000149742Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000067656Ensembl, 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

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

Membrane proteins, carrier proteins: membrane transport proteins solute carrier (TC 2A)
By group
SLC1–10
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SLC11–20
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SLC21–30
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SLC31–40
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SLC41–48
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SLCO1–4
Ion pumps
Symporter, Cotransporter
Antiporter (exchanger)
see also solute carrier disorders


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