Solute carrier family 10 member 4

SLC10A4
Identifiers
Aliases	SLC10A4, P4, solute carrier family 10 member 4
External IDs	MGI: 3606480 HomoloGene: 15495 GeneCards: SLC10A4
Gene location (Human)
Chr.	Chromosome 4 (human)[1]
End	48,489,196 bp[1]
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)[2]
End	73,012,955 bp[2]
Gene ontology
Molecular function	• symporter activity; • bile acid:sodium symporter activity;
Cellular component	• integral component of membrane; • plasma membrane; • membrane;
Biological process	• ion transport; • transmembrane transport; • sodium ion transport; • bile acid and bile salt transport;
	Sources:Amigo / QuickGO
Orthologs
	201780
	231290
	ENSG00000145248
	ENSMUSG00000029219
	Q96EP9
	Q3UEZ8
	NM_152679
	NM_173403
	NP_689892
	NP_775579
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 10 member 4 is a protein that in humans is encoded by the SLC10A4 gene.^[5] In mice, it appears to promote acidification of synaptic vesicles containing monoamines, enhancing their uptake, and is co-expressed with VMAT2 and VAChT.^[6]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000145248 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000029219 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ "Entrez Gene: Solute carrier family 10 member 4". Retrieved 2016-04-17.
↑ Larhammar M, Patra K, Blunder M, Emilsson L, Peuckert C, Arvidsson E, Rönnlund D, Preobraschenski J, Birgner C, Limbach C, Widengren J, Blom H, Jahn R, Wallén-Mackenzie Å, Kullander K (March 2015). "SLC10A4 is a vesicular amine-associated transporter modulating dopamine homeostasis". Biological Psychiatry. 77 (6): 526–36. doi:10.1016/j.biopsych.2014.07.017. PMID 25176177.