Solute carrier family 38 member 5: Difference between revisions

Jump to navigation Jump to search
VisualWikitext
m (links)
 
imported>KolbertBot
m (Bot: HTTP→HTTPS (v478))
Line 5: Line 5:
{{cite web
{{cite web
| title = Entrez Gene: Solute carrier family 38 member 5
| title = Entrez Gene: Solute carrier family 38 member 5
| url = http://www.ncbi.nlm.nih.gov/gene/92745
| url = https://www.ncbi.nlm.nih.gov/gene/92745
| accessdate = 2017-10-07
| accessdate = 2017-10-07
}}</ref>
}}</ref>

Revision as of 14:13, 20 December 2017

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

n/a

n/a

Ensembl

n/a

n/a

UniProt

n/a

n/a

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.

Retrieved from "https://www.wikidoc.org/index.php?title=Solute_carrier_family_38_member_5&oldid=1534487"