The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
Gene Review

TRL-AAG2-1  -  transfer RNA-Leu (AAG) 2-1

Homo sapiens

Synonyms: TRL1, TRNAL1, TRNP1
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.

Disease relevance of TRNAL1


High impact information on TRNAL1


Anatomical context of TRNAL1

  • This reflected common interaction at receptors that probably included both beta-VLDL and B/E receptors, since: (1) in fresh macrophages, VLDL from hypertriglyceridemic subjects partially displaced beta-VLDL; (2) in B/E receptor-repressed macrophages, TRL1 maintained capacity to totally displace beta-VLDL [9].

Other interactions of TRNAL1

  • Degradation of 125I-labeled TRL1 was greater than that of 125I-labeled TRL2 [9].


  1. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation. Smith, P.R., Bain, S.C., Good, P.A., Hattersley, A.T., Barnett, A.H., Gibson, J.M., Dodson, P.M. Ophthalmology (1999) [Pubmed]
  2. A new approach to apple proliferation detection: a highly sensitive real-time PCR assay. Baric, S., Dalla-Via, J. J. Microbiol. Methods (2004) [Pubmed]
  3. A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy. Garcia-Lozano, J.R., Aguilera, I., Bautista, J., Nuñez-Roldan, A. Hum. Mutat. (2000) [Pubmed]
  4. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Reardon, W., Ross, R.J., Sweeney, M.G., Luxon, L.M., Pembrey, M.E., Harding, A.E., Trembath, R.C. Lancet (1992) [Pubmed]
  5. Role of mitochondrial DNA tRNA leucine and glucagon receptor missense mutations in Utah white diabetic patients. Elbein, S.C., Hoffman, M.D. Diabetes Care (1996) [Pubmed]
  6. Links between plant and rhizoplane bacterial communities in grassland soils, characterized using molecular techniques. Nunan, N., Daniell, T.J., Singh, B.K., Papert, A., McNicol, J.W., Prosser, J.I. Appl. Environ. Microbiol. (2005) [Pubmed]
  7. A molecular phylogeny of the hawkmoth genus Hyles (Lepidoptera: Sphingidae, Macroglossinae). Hundsdoerfer, A.K., Kitching, I.J., Wink, M. Mol. Phylogenet. Evol. (2005) [Pubmed]
  8. Amino acid pools in cultured muscle cells. Low, R.B., Stirewalt, W.S., Rittling, S.R., Woodworth, R.C. J. Cell. Biochem. (1984) [Pubmed]
  9. Metabolism of human plasma triacylglycerol-rich lipoproteins in rodent macrophages: capacity for interaction at beta-VLDL receptor. Nestel, P.J., Billington, T., Bazelmans, J. Biochim. Biophys. Acta (1985) [Pubmed]
WikiGenes - Universities