Solute carrier family 38 member 5: Difference between revisions

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==Function==
==Function==


The protein encoded by this gene is a system N sodium-coupled [[amino acid transporter]]. The encoded protein transports [[glutamine]], [[asparagine]], [[histidine]], [[serine]], [[alanine]], and [[glycine]] across the [[cell membrane]], but does not transport charged amino acids, [[Imino acid|imino acids]], or [[N-alkylated amino acid|N-alkylated amino acids]]. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined.
The protein encoded by this gene is a system N sodium-coupled [[amino acid transporter]]. The encoded protein transports [[glutamine]], [[asparagine]], [[histidine]], [[serine]], [[alanine]], and [[glycine]] across the [[cell membrane]], but does not transport charged amino acids, [[imino acid]]s, or [[N-alkylated amino acid]]s. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined.


== References ==
== References ==
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Latest revision as of 10:12, 12 January 2019

VALUE_ERROR (nil)
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 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene. [1]

Function

The protein encoded by this gene is a system N sodium-coupled amino acid transporter. The encoded protein transports glutamine, asparagine, histidine, serine, alanine, and glycine across the cell membrane, but does not transport charged amino acids, imino acids, or N-alkylated amino acids. Alternative splicing results in multiple transcript variants, but the full-length nature of some of these variants has not been determined.

References

  1. "Entrez Gene: Solute carrier family 38 member 5". Retrieved 2017-10-07.

Further reading

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