SLC2A12

Last updated
SLC2A12
Identifiers
Aliases SLC2A12 , GLUT12, GLUT8, solute carrier family 2 member 12
External IDs OMIM: 610372 MGI: 3052471 HomoloGene: 59263 GeneCards: SLC2A12
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_145176

NM_178934

RefSeq (protein)

NP_660159

NP_849265

Location (UCSC) Chr 6: 133.99 – 134.05 Mb Chr 10: 22.52 – 22.58 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 2, facilitated glucose transporter member 12 is a protein that in humans is encoded by the SLC2A12 gene. [5] [6] [7]

Contents

See also

Related Research Articles

Glucose transporter 3, also known as solute carrier family 2, facilitated glucose transporter member 3 (SLC2A3) is a protein that in humans is encoded by the SLC2A3 gene. GLUT3 facilitates the transport of glucose across the plasma membranes of mammalian cells. GLUT3 is most known for its specific expression in neurons and has originally been designated as the neuronal GLUT. GLUT3 has been studied in other cell types with specific glucose requirements, including sperm, preimplantation embryos, circulating white blood cells and carcinoma cell lines.

<span class="mw-page-title-main">Thiamine transporter 2</span> Protein-coding gene in the species Homo sapiens

Thiamine transporter 2 (ThTr-2), also known as solute carrier family 19 member 3, is a protein that in humans is encoded by the SLC19A3 gene. SLC19A3 is a thiamine transporter.

<span class="mw-page-title-main">GLUT5</span> Protein-coding gene in the species Homo sapiens

GLUT5 is a fructose transporter expressed on the apical border of enterocytes in the small intestine. GLUT5 allows for fructose to be transported from the intestinal lumen into the enterocyte by facilitated diffusion due to fructose's high concentration in the intestinal lumen. GLUT5 is also expressed in skeletal muscle, testis, kidney, fat tissue (adipocytes), and brain.

<span class="mw-page-title-main">Sodium-coupled neutral amino acid transporter 2</span> Protein-coding gene in the species Homo sapiens

Sodium-coupled neutral amino acid transporter 2 is a protein that in humans is encoded by the SLC38A2 gene.

<span class="mw-page-title-main">SLC26A6</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 26 member 6 is a protein that in humans is encoded by the SLC26A6 gene. It is an anion-exchanger expressed in the apical membrane of the kidney proximal tubule, the apical membranes of the duct cells in the pancreas, and the villi of the duodenum.

<span class="mw-page-title-main">SLC2A10</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 2, facilitated glucose transporter member 10 is a protein that in humans is encoded by the SLC2A10 gene.

<span class="mw-page-title-main">Multidrug and toxin extrusion protein 1</span> Protein-coding gene in the species Homo sapiens

Multidrug and toxin extrusion protein 1 (MATE1), also known as solute carrier family 47 member 1, is a protein that in humans is encoded by the SLC47A1 gene. SLC47A1 belongs to the MATE family of transporters that are found in bacteria, archaea and eukaryotes.

<span class="mw-page-title-main">Urea transporter 2</span> Protein-coding gene in the species Homo sapiens

Urea transporter 2 is a protein that in humans is encoded by the SLC14A2 gene.

<span class="mw-page-title-main">SLC2A6</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 2, facilitated glucose transporter member 6 is a protein that in humans is encoded by the SLC2A6 gene.

<span class="mw-page-title-main">SLC6A14</span> Protein-coding gene in the species Homo sapiens

Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) (SLC6A14) is a protein that in humans is encoded by the SLC6A14 gene.

<span class="mw-page-title-main">Solute carrier organic anion transporter family member 2B1</span> Protein-coding gene in the species Homo sapiens

Solute carrier organic anion transporter family member 2B1 also known as organic anion-transporting polypeptide 2B1 (OATP2B1) is a protein that in humans is encoded by the gene SLCO2B1.

<span class="mw-page-title-main">Sodium-coupled monocarboxylate transporter 1</span> Protein-coding gene in the species Homo sapiens

Sodium-coupled monocarboxylate transporter 1 is a protein that in humans is encoded by the SLC5A8 gene.

<span class="mw-page-title-main">SLC2A9</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 2, facilitated glucose transporter member 9 is a protein that in humans is encoded by the SLC2A9 gene.

<span class="mw-page-title-main">SLC13A3</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 13 member 3 also called sodium-dependent dicarboxylate transporter (NaDC3) is a protein that in humans is encoded by the SLC13A3 gene.

<span class="mw-page-title-main">SLC22A9</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene.

<span class="mw-page-title-main">SLC2A7</span> Protein-coding gene in the species Homo sapiens

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.

<span class="mw-page-title-main">Asc-type amino acid transporter 1</span> Protein-coding gene in the species Homo sapiens

Asc-type amino acid transporter 1 (Asc-1) is a protein that in humans is encoded by the SLC7A10 gene.

<span class="mw-page-title-main">SLC22A25</span> Protein-coding gene in the species Homo sapiens

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.

<span class="mw-page-title-main">Monocarboxylate transporter 10</span> Protein-coding gene in the species Homo sapiens

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">SLC2A14</span> Protein-coding gene in the species Homo sapiens

Solute carrier family 2, member 14 is a protein that in humans is encoded by the SLC2A14 gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000146411 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000037490 - 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. Joost HG, Thorens B (Jan 2002). "The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review)". Mol Membr Biol. 18 (4): 247–56. doi: 10.1080/09687680110090456 . PMID   11780753. S2CID   22667943.
  6. Rogers S, Macheda ML, Docherty SE, Carty MD, Henderson MA, Soeller WC, Gibbs EM, James DE, Best JD (Feb 2002). "Identification of a novel glucose transporter-like protein-GLUT-12". Am J Physiol Endocrinol Metab. 282 (3): E733–8. doi:10.1152/ajpendo.2002.282.3.E733. PMID   11832379. S2CID   22919544.
  7. "Entrez Gene: SLC2A12 solute carrier family 2 (facilitated glucose transporter), member 12".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.