SLC22A15 | |||||||||||||||||||||||||
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Identifiers | |||||||||||||||||||||||||
Aliases | SLC22A15 , FLIPT1, PRO34686, solute carrier family 22 member 15 | ||||||||||||||||||||||||
External IDs | OMIM: 608275 MGI: 3607704 HomoloGene: 41263 GeneCards: SLC22A15 | ||||||||||||||||||||||||
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Orthologs | |||||||||||||||||||||||||
Species | Human | Mouse | |||||||||||||||||||||||
Entrez | |||||||||||||||||||||||||
Ensembl | |||||||||||||||||||||||||
UniProt | |||||||||||||||||||||||||
RefSeq (mRNA) | |||||||||||||||||||||||||
RefSeq (protein) | |||||||||||||||||||||||||
Location (UCSC) | Chr 1: 115.98 – 116.07 Mb | Chr 3: 101.86 – 101.92 Mb | |||||||||||||||||||||||
PubMed search | [3] | [4] | |||||||||||||||||||||||
Wikidata | |||||||||||||||||||||||||
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Solute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene. [5]
Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, hormones, neurotransmitters, and cellular metabolites. These transporters are also referred to as amphiphilic solute facilitators (ASFs).
Zinc transporter ZIP4 is a transmembrane protein which in humans is encoded by the SLC39A4 gene. It is associated with acrodermatitis enteropathica.
Probable low affinity copper uptake protein 2 is a protein that in humans is encoded by the SLC31A2 gene.
Solute carrier family 2, facilitated glucose transporter member 6 is a protein that in humans is encoded by the SLC2A6 gene.
Solute carrier family 6, member 18 also known as SLC6A18 is a protein which in humans is encoded by the SLC6A18 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.
Solute carrier family 2, facilitated glucose transporter member 7 also known as glucose transporter 7 (GLUT7) is a protein that in humans is encoded by the SLC2A7 gene.
Solute carrier family 22 member 25 (SLC22A25), also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC22A25 gene.
Monocarboxylate transporter 10, also known as aromatic amino acid transporter 1 and T-type amino acid transporter 1 (TAT1) and solute carrier family 16 member 10 (SLC16A10), is a protein that in humans is encoded by the SLC16A10 gene. SLC16A10 is a member of the solute carrier family.
Zinc transporter 3 also known as solute carrier family 30 member 3 is a protein in humans that is encoded by the SLC30A3 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+-Pi 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 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene.
Solute carrier family 22 member 13 is a protein that in humans is encoded by the SLC22A13 gene.
Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene.
SLC45A1 is a member of the SLC45 family of solute carriers. Analysis of the protein function in a recombinant yeast expression assay show that it can: (i) transport a disaccharide, such as glucose and sucrose (ii) perform secondary active transport in a proton-dependent manner.
Solute carrier family 22 member 14 is a protein that in humans is encoded by the SLC22A14 gene.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.