Monocarboxylate transporter 9: Difference between revisions
Jump to navigation
Jump to search
m Bot: HTTP→HTTPS |
imported>JCW-CleanerBot m →Further reading: task, replaced: Pflugers Arch → Pflügers Arch using AWB |
||
| Line 5: | Line 5: | ||
== Clinical relevance == | == Clinical relevance == | ||
Mutations in the SLC16A9 gene have been associated with [[carnitine]] levels in blood.<ref name="pmid21886157">{{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 }}</ref> | Mutations in the SLC16A9 gene have been associated with [[carnitine]] levels in blood.<ref name="pmid21886157">{{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 }}</ref> | ||
== References == | == References == | ||
| Line 18: | Line 18: | ||
*{{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=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=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 }} | *{{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= | *{{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}} | {{refend}} | ||
Latest revision as of 16:05, 29 June 2018
| VALUE_ERROR (nil) | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Aliases | |||||||
| External IDs | GeneCards: [1] | ||||||
| Orthologs | |||||||
| Species | Human | Mouse | |||||
| Entrez |
|
| |||||
| Ensembl |
|
| |||||
| UniProt |
|
| |||||
| RefSeq (mRNA) |
|
| |||||
| RefSeq (protein) |
|
| |||||
| Location (UCSC) | n/a | n/a | |||||
| PubMed search | n/a | n/a | |||||
| Wikidata | |||||||
| |||||||
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
- ↑ "Entrez Gene: solute carrier family 16".
- ↑ 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. PMC 3832838. PMID 21886157.
Further reading
- Kolz M, Johnson T, Sanna S, et al. (2009). "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations". PLoS Genet. 5 (6): e1000504. doi:10.1371/journal.pgen.1000504. PMC 2683940. PMID 19503597.
- Gunjaca G; Boban M; Pehlić M; et al. (2010). "Predictive value of 8 genetic loci for serum uric acid concentration". Croat. Med. J. 51 (1): 23–31. doi:10.3325/cmj.2010.51.23. PMC 2829178. PMID 20162742.
- Grupe A, Li Y, Rowland C, et al. (2006). "A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease". Am. J. Hum. Genet. 78 (1): 78–88. doi:10.1086/498851. PMC 1380225. PMID 16385451.
- Polasek O; Jeroncić I; Mulić R; et al. (2010). "Common variants in SLC17A3 gene affect intra-personal variation in serum uric acid levels in longitudinal time series". Croat. Med. J. 51 (1): 32–9. doi:10.3325/cmj.2010.51.32. PMC 2829186. PMID 20162743.
- Stark K, Reinhard W, Grassl M, et al. (2009). "Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease". PLoS ONE. 4 (11): e7729. doi:10.1371/journal.pone.0007729. PMC 2766838. PMID 19890391.
- van der Harst P, Bakker SJ, de Boer RA, et al. (2010). "Replication of the five novel loci for uric acid concentrations and potential mediating mechanisms". Hum. Mol. Genet. 19 (2): 387–95. doi:10.1093/hmg/ddp489. PMID 19861489.
- Illig T, Gieger C, Zhai G, et al. (2010). "A genome-wide perspective of genetic variation in human metabolism". Nat. Genet. 42 (2): 137–41. doi:10.1038/ng.507. PMC 3773904. PMID 20037589.
- Halestrap AP, Meredith D (2004). "The SLC16 gene family-from monocarboxylate transporters (MCTs) to aromatic amino acid transporters and beyond". Pflügers Arch. 447 (5): 619–28. doi:10.1007/s00424-003-1067-2. PMID 12739169.
| Stub icon | This membrane protein–related article is a stub. You can help Wikipedia by expanding it. |
