| 释义 |
- Clinical relevance
- References
- Further reading
{{Infobox_gene}}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] References 1. ^{{cite web | title = Entrez Gene: solute carrier family 16| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=220963| accessdate = }}
2. ^{{cite journal |vauthors=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 | title = Human metabolic individuality in biomedical and pharmaceutical research | journal = Nature | volume = 477 | issue = 7362 | pages = 54–60 |date=September 2011 | pmid = 21886157 | doi = 10.1038/nature10354 | pmc = 3832838 }}
Further reading {{refbegin | 2}}- {{cite journal |vauthors=Kolz M, Johnson T, Sanna S, etal |title=Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. |journal=PLoS Genet. |volume=5 |issue= 6 |pages= e1000504 |year= 2009 |pmid= 19503597 |doi= 10.1371/journal.pgen.1000504 |pmc=2683940}}
- {{cite journal |author1=Gunjaca G |author2=Boban M |author3=Pehlić M |title=Predictive value of 8 genetic loci for serum uric acid concentration. |journal=Croat. Med. J. |volume=51 |issue= 1 |pages= 23–31 |year= 2010 |pmid= 20162742 |doi= 10.3325/cmj.2010.51.23|pmc=2829178|display-authors=etal}}
- {{cite journal |vauthors=Grupe A, Li Y, Rowland C, etal |title=A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease. |journal=Am. J. Hum. Genet. |volume=78 |issue= 1 |pages= 78–88 |year= 2006 |pmid= 16385451 |doi= 10.1086/498851 |pmc=1380225}}
- {{cite journal |author1=Polasek O |author2=Jeroncić I |author3=Mulić R |title=Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series. |journal=Croat. Med. J. |volume=51 |issue= 1 |pages= 32–9 |year= 2010 |pmid= 20162743 |doi= 10.3325/cmj.2010.51.32|pmc=2829186|display-authors=etal}}
- {{cite journal |vauthors=Stark K, Reinhard W, Grassl M, etal |title=Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease. |journal=PLoS ONE |volume=4 |issue= 11 |pages= e7729 |year= 2009 |pmid= 19890391 |doi= 10.1371/journal.pone.0007729 |pmc=2766838}}
- {{cite journal |vauthors=van der Harst P, Bakker SJ, de Boer RA, etal |title=Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms. |journal=Hum. Mol. Genet. |volume=19 |issue= 2 |pages= 387–95 |year= 2010 |pmid= 19861489 |doi= 10.1093/hmg/ddp489 }}
- {{cite journal |vauthors=Illig T, Gieger C, Zhai G, etal |title=A genome-wide perspective of genetic variation in human metabolism. |journal=Nat. Genet. |volume=42 |issue= 2 |pages= 137–41 |year= 2010 |pmid= 20037589 |doi= 10.1038/ng.507 |pmc=3773904 }}
- {{cite journal |vauthors=Halestrap AP, Meredith D |title=The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond. |journal=Pflügers Arch. |volume=447 |issue= 5 |pages= 619–28 |year= 2004 |pmid= 12739169 |doi= 10.1007/s00424-003-1067-2 }}
{{refend}}{{Membrane transport proteins}}{{membrane-protein-stub}} 2 : Human proteins|Solute carrier family |