SLC15A4

SLC15A4
Identifiers
Aliases	SLC15A4, PHT1, PTR4, FP12591, solute carrier family 15 member 4
External IDs	OMIM: 615806 MGI: 2140796 HomoloGene: 26432 GeneCards: SLC15A4
Gene location (Human)
Chr.	Chromosome 12 (human)[1]
End	128,823,958 bp[1]
Gene location (Mouse)
Chr.	Chromosome 5 (mouse)[2]
End	127,632,897 bp[2]
Gene ontology
Molecular function	• symporter activity; • transporter activity; • peptide:proton symporter activity; • GO:0001948 protein binding; • GO:0022891 transmembrane transporter activity; • L-histidine transmembrane transporter activity; • oligopeptide transmembrane transporter activity; • peptide transmembrane transporter activity;
Cellular component	• lysosomal membrane; • membrane; • integral component of membrane; • cell membrane; • specific granule membrane;
Biological process	• oligopeptide transport; • protein transport; • ion transport; • peptide transport; • transmembrane transport; • neutrophil degranulation; • hydrogen ion transmembrane transport; • histidine transport; • oligopeptide transmembrane transport; • L-histidine transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	121260
	100561
	ENSG00000139370
	ENSMUSG00000029416
	Q8N697
	Q91W98
	NM_145648
	NM_133895
	NP_663623
	NP_598656
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 15, member 4 is a protein in humans that is encoded by the SLC15A4 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000139370 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000029416 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: Solute carrier family 15, member 4". Retrieved 2013-07-08.