Solute carrier family 9 member a4

SLC9A4
Identifiers
Aliases	SLC9A4, NHE4, solute carrier family 9 member A4
External IDs	OMIM: 600531 MGI: 105074 HomoloGene: 72232 GeneCards: SLC9A4
Gene location (Human)
Chr.	Chromosome 2 (human)[1]
End	102,533,972 bp[1]
Gene location (Mouse)
Chr.	Chromosome 1 (mouse)[2]
End	40,630,725 bp[2]
Gene ontology
Molecular function	• solute:proton antiporter activity; • antiporter activity; • sodium:proton antiporter activity; • potassium:proton antiporter activity;
Cellular component	• integral component of membrane; • basolateral plasma membrane; • apical plasma membrane; • membrane; • cell membrane;
Biological process	• gastric acid secretion; • hydrogen ion transmembrane transport; • epithelial cell development; • cation transport; • ion transport; • regulation of pH; • sodium ion transport; • regulation of intracellular pH; • sodium ion import across plasma membrane; • potassium ion transmembrane transport; • transmembrane transport; • anion transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	389015
	110895
	ENSG00000180251
	ENSMUSG00000026065
	Q6AI14
	Q8BUE1
	NM_001011552
	NM_177084
	NP_001011552
	NP_796058
	Wikidata
View/Edit Human	View/Edit Mouse

Solute carrier family 9 member A4 is a protein that in humans is encoded by the SLC9A4 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000180251 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000026065 - 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 9 member A4". Retrieved 2016-10-26.