SLC17A9

SLC17A9
Identifiers
Aliases	SLC17A9 , C20orf59, VNUT, POROK8, solute carrier family 17 member 9
External IDs	OMIM: 612107 MGI: 1919107 HomoloGene: 76562 GeneCards: SLC17A9
Gene location (Human)
Chr.	Chromosome 20 (human)
End	62,969,585 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	180,384,073 bp
RNA expression pattern
	Top expressed in
	right lobe of liver; ; stromal cell of endometrium; ; spleen; ; pylorus; ; bone marrow cells; ; body of stomach; ; pancreatic ductal cell; ; lymph node; ; ascending aorta; ; fundus;
	Top expressed in
	large intestine; ; colon; ; molar; ; left colon; ; spermatocyte; ; spleen; ; blood; ; yolk sac; ; duodenum; ; thymus;
	More reference expression data
	n/a
Gene ontology
Molecular function	transmembrane transporter activity ; transporter activity ;
Cellular component	integral component of membrane ; membrane ;
Biological process	anion transport ; transmembrane transport ; exocytosis ;
	Sources:Amigo / QuickGO
Orthologs
	63910
	228993
	ENSG00000101194
	ENSMUSG00000023393
	Q9BYT1
	Q8VCL5
	NM_001302643 ; NM_022082
	NM_183161
	NP_001289572 ; NP_071365
	NP_898984
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated October 18, 2022

Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. ^[5]

Function

This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants.

Related Research Articles

UDP-xylose and UDP-N-acetylglucosamine transporter is a protein that in humans is encoded by the SLC35B4 gene.

Vesicular inhibitory amino acid transporter is a protein that in humans is encoded by the SLC32A1 gene.

Vesicular glutamate transporter 1 (VGLUT1) is a protein that in humans is encoded by the SLC17A7 gene.

Zinc transporter ZIP10, also known as solute carrier family 39 member 10, is a protein that in humans is encoded by the SLC39A10 gene. ZIP10 belongs to a subfamily of proteins that show structural characteristics of zinc transporters, and have 14 members in the human genome: ZIP1, ZIP2, ZIP3, ZIP4, ZIP5, ZIP6, ZIP7, ZIP8, ZIP9, ZIP10, ZIP11, ZIP12, ZIP13 and ZIP14.

Sodium/hydrogen exchanger 10, also known as solute carrier family 9 member 10, is a protein that in humans is encoded by the SLC9A10 gene.

Sodium/hydrogen exchanger 11, also known as solute carrier family 9, member 11, is a protein that in humans is encoded by the SLC9A11 gene. SLC9A11 is a member of the sodium-hydrogen exchanger (NHE) family.

Vesicular glutamate transporter 3 (VGLUT3) is a protein that in humans is encoded by the SLC17A8 gene.

Solute carrier family 25, member 16 is a protein in humans that is encoded by the SLC25A16 gene.

Monocarboxylate transporter 6 (MCT6) is a protein in humans that is encoded by the SLC16A5 gene.

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

Solute carrier family 7, member 14 is a protein that in humans is encoded by the SLC7A14 gene.

Glucose-6-phosphate exchanger SLC37A2 is a protein that in humans is encoded by the SLC37A2 gene.

Sodium-dependent phosphate transport protein 2A, also known as Na⁺-P_i cotransporter 2a (NaPi-2a), is a protein in humans that is encoded by the SLC34A1 gene. This gene encodes a member of the type II sodium-phosphate cotransporter family.

Solute carrier family 17, member 6 is a protein that in humans is encoded by the SLC17A6 gene.

Solute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene.

Solute carrier family 22 member 24 is a protein that in humans is encoded by the SLC22A24 gene.

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

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

Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.

Solute carrier family 22 member 14 is a protein that in humans is encoded by the SLC22A14 gene.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000101194 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000023393 - 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 17 member 9" . Retrieved 2016-07-27.

SLC17A9

Contents

Function

Related Research Articles

References

Further reading