Solute carrier family 22 member 13 is a protein that in humans is encoded by the SLC22A13 gene. [5]

SLC22A13
Identifiers
AliasesSLC22A13, OAT10, OCTL1, OCTL3, ORCTL-3, ORCTL3, solute carrier family 22 member 13
External IDsOMIM: 604047; MGI: 2143107; HomoloGene: 3140; GeneCards: SLC22A13; OMA:SLC22A13 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004256

NM_133980

RefSeq (protein)

NP_004247

NP_598741

Location (UCSC)Chr 3: 38.27 – 38.28 MbChr 9: 119.02 – 119.04 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 4. The encoded protein is a transmembrane protein involved in the transport of small molecules. This protein can function to mediate urate uptake and is a high affinity nicotinate exchanger in the kidneys and the intestine.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000172940Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000074028Ensembl, 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. ^ "Entrez Gene: Solute carrier family 22 member 13". Retrieved 2017-10-05.

Further reading

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