Monocarboxylate transporter 9

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Aliases SLC16A9, C10orf36, MCT9, solute carrier family 16 member 9
External IDs MGI: 1914109 HomoloGene: 32642 GeneCards: SLC16A9
Species Human Mouse
RefSeq (mRNA)


RefSeq (protein)


Location (UCSC) Chr 10: 59.65 – 59.74 Mb Chr 10: 70.25 – 70.29 Mb
PubMed search [1] [2]
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Monocarboxylate transporter 9 (MCT9, solute carrier family 16, member 9, SLC16A9) is a protein that in humans is encoded by the SLC16A9 gene.[3]

Clinical relevance[edit]

Mutations in the SLC16A9 gene have been associated with carnitine levels in blood.[4]


  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ "Entrez Gene: solute carrier family 16". 
  4. ^ Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Römisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C, Assimes TL, Deloukas P, Erdmann J, Holm H, Kathiresan S, König IR, McPherson R, Reilly MP, Roberts R, Samani NJ, Schunkert H, Stewart AF (September 2011). "Human metabolic individuality in biomedical and pharmaceutical research". Nature. 477 (7362): 54–60. PMID 21886157. doi:10.1038/nature10354. 

Further reading[edit]