Open Access Articles- Top Results for Monocarboxylate transporter 9

Monocarboxylate transporter 9

SymbolsSLC16A9 ; C10orf36; MCT9
External IDsOMIM614242 MGI1914109 HomoloGene32642 IUPHAR: 997 GeneCards: SLC16A9 Gene
RefSeq (mRNA)NM_194298NM_025807
RefSeq (protein)NP_919274NP_080083
Location (UCSC)Chr 10:
61.41 – 61.5 Mb
Chr 10:
70.25 – 70.29 Mb
PubMed search[1][2]

Monocarboxylate transporter 9 (MCT9, solute carrier family 16, member 9, SLC16A9) is a protein that in humans is encoded by the SLC16A9 gene.[1]

Clinical relevance

Mutations in the SLC16A9 gene have been associated with carnitine levels in blood.[2]


  1. ^ "Entrez Gene: solute carrier family 16". 
  2. ^ 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


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