SLC16A9

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Solute carrier family 16, member 9 (monocarboxylic acid transporter 9)
Identifiers
Symbols SLC16A9 ; C10orf36; MCT9
External IDs OMIM614242 MGI1914109 HomoloGene32642 GeneCards: SLC16A9 Gene
Orthologs
Species Human Mouse
Entrez 220963 66859
Ensembl ENSG00000165449 ENSMUSG00000037762
UniProt Q7RTY1 Q7TM99
RefSeq (mRNA) NM_194298 NM_025807
RefSeq (protein) NP_919274 NP_080083
Location (UCSC) Chr 10:
61.41 – 61.5 Mb
Chr 10:
70.25 – 70.29 Mb
PubMed search [1] [2]

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

Clinical relevance[edit]

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

References[edit]

  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. doi:10.1038/nature10354. PMID 21886157. 

Further reading[edit]