Monocarboxylate transporter 6

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

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

AliasesSLC16A5, MCT5, MCT6, solute carrier family 16 member 5, Monocarboxylate transporter 6
End75,106,162 bp[1]
Quick facts SLC16A5, Identifiers ...
SLC16A5
Identifiers
AliasesSLC16A5, MCT5, MCT6, solute carrier family 16 member 5, Monocarboxylate transporter 6
External IDsOMIM: 603879; MGI: 2443515; HomoloGene: 20985; GeneCards: SLC16A5; OMA:SLC16A5 - orthologs
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 MbChr 11: 115.35 – 115.37 Mb
PubMed search[3][4]
Wikidata
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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].

References

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