Monocarboxylate transporter 6

Last updated
SLC16A5
Identifiers
Aliases SLC16A5 , MCT5, MCT6, solute carrier family 16 member 5, Monocarboxylate transporter 6
External IDs OMIM: 603879 MGI: 2443515 HomoloGene: 20985 GeneCards: SLC16A5
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001271765
NM_004695
NM_001369668

NM_001080934
NM_001359606
NM_001359608
NM_001359609

RefSeq (protein)

NP_001258694
NP_004686
NP_001356597

NP_001074403
NP_001346535
NP_001346537
NP_001346538

Location (UCSC) Chr 17: 75.09 – 75.11 Mb Chr 11: 115.35 – 115.37 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Monocarboxylate transporter 6 (MCT6) is a protein in humans that is encoded by the SLC16A5 gene. [5]

This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012].

Related Research Articles

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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.

<span class="mw-page-title-main">Mitochondrial glycine transporter</span>

Mitochondrial glycine transporter is a protein that in humans is encoded by the SLC25A38 gene. SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.

<span class="mw-page-title-main">Monocarboxylate transporter 10</span>

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.

<span class="mw-page-title-main">Monocarboxylate transporter 9</span>

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<span class="mw-page-title-main">Glucose-6-phosphate exchanger SLC37A2</span> Biological protein

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<span class="mw-page-title-main">Monocarboxylate transporter 2</span>

Monocarboxylate transporter 2 (MCT2) also known as solute carrier family 16 member 7 (SLC16A7) is a protein that in humans is encoded by the SLC16A7 gene. MCT2 is a proton-coupled monocarboxylate transporter. It catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate and beta-hydroxybutyrate. It also functions as high-affinity pyruvate transporter.

<span class="mw-page-title-main">Monocarboxylate transporter 3</span>

Monocarboxylate transporter 3 (MCT3) also known as solute carrier family 16 member 8 is a protein that in humans is encoded by the SLC16A8 gene. MCT is a proton-coupled monocarboxylate transporter. It catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactate, pyruvate, branched-chain oxo acids derived from leucine, valine and isoleucine, and the ketone bodies acetoacetate, beta-hydroxybutyrate and acetate. It also functions as high-affinity pyruvate transporter.

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<span class="mw-page-title-main">Solute carrier family 17 (vesicular glutamate transporter), member 6</span>

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<span class="mw-page-title-main">Solute carrier family 22 member 15</span> Protein-coding gene in the species Homo sapiens

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

<span class="mw-page-title-main">SLC17A9</span>

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

<span class="mw-page-title-main">SLC22A13</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">SLC38A5</span> Protein-coding gene in the species Homo sapiens

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

<span class="mw-page-title-main">SLC22A14</span>

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References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000170190 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000045775 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Solute carrier family 16, member 5 (monocarboxylic acid transporter 6)".