Monocarboxylate transporter 2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

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.[5] MCT2 is a proton-coupled monocarboxylate transporter. It catalyzes the rapid transport across the plasma membrane of many monocarboxylates such as lactic acid, 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.

AliasesSLC16A7, MCT2, solute carrier family 16 member 7
End59,789,855 bp[1]
Quick facts SLC16A7, Identifiers ...
SLC16A7
Identifiers
AliasesSLC16A7, MCT2, solute carrier family 16 member 7
External IDsOMIM: 603654; MGI: 1330284; HomoloGene: 20990; GeneCards: SLC16A7; OMA:SLC16A7 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001270622
NM_001270623
NM_004731

NM_011391
NM_001358496
NM_001358915

RefSeq (protein)

NP_001257551
NP_001257552
NP_004722

NP_035521
NP_001345425
NP_001345844

Location (UCSC)Chr 12: 59.6 – 59.79 MbChr 10: 125.06 – 125.23 Mb
PubMed search[3][4]
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Both Northern blot analysis and inspection of the human expressed sequence tag (EST) database suggest relatively little expression of MCT2 in human tissues. As well, the sequence of MCT2 is far less conserved across species than that of MCT1 or MCT4 and there also appear to be considerable species differences in the tissue expression profile of this isoform.

Of the four known mammalian lactate transporters (MCTs 1-4), MCT2 harbors the highest affinity for lactate.[6] In parallel, MCT2 gene transcription has been demonstrated to respond with high-sensitivity to hypoxia, intracellular pH, and, to lactate.[7]

See also

References

Further reading

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