SLC22A13: Difference between revisions

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{{cite web
{{cite web
| title = Entrez Gene: Solute carrier family 22 member 13
| title = Entrez Gene: Solute carrier family 22 member 13
| url = http://www.ncbi.nlm.nih.gov/gene/9390
| url = https://www.ncbi.nlm.nih.gov/gene/9390
| accessdate = 2017-10-05
| accessdate = 2017-10-05
}}</ref>
}}</ref>

Latest revision as of 12:47, 20 December 2017

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Solute carrier family 22 member 13 is a protein that in humans is encoded by the SLC22A13 gene. [1]

Function

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

  1. "Entrez Gene: Solute carrier family 22 member 13". Retrieved 2017-10-05.

Further reading


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