SLC6A5

SLC6A5

Solute carrier family 6 (neurotransmitter transporter, glycine), member 5, also known as SLC6A5, is a human gene.cite web | title = Entrez Gene: SLC6A5 solute carrier family 6 (neurotransmitter transporter, glycine), member 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9152| accessdate = ]

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ee also

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* Solute carrier family

References

Further reading

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*cite journal | author=López-Corcuera B, Aragón C, Geerlings A |title=Regulation of glycine transporters. |journal=Biochem. Soc. Trans. |volume=29 |issue= Pt 6 |pages= 742–5 |year= 2002 |pmid= 11709067 |doi=
*cite journal | author=Morrow JA, Collie IT, Dunbar DR, "et al." |title=Molecular cloning and functional expression of the human glycine transporter GlyT2 and chromosomal localisation of the gene in the human genome. |journal=FEBS Lett. |volume=439 |issue= 3 |pages= 334–40 |year= 1998 |pmid= 9845349 |doi=
*cite journal | author=Gallagher MJ, Burgess LH, Brunden KR |title=Characterization of multiple forms of the human glycine transporter type-2. |journal=Brain Res. Mol. Brain Res. |volume=70 |issue= 1 |pages= 101–15 |year= 1999 |pmid= 10381548 |doi=
*cite journal | author=Evans J, Herdon H, Cairns W, "et al." |title=Cloning, functional characterisation and population analysis of a variant form of the human glycine type 2 transporter. |journal=FEBS Lett. |volume=463 |issue= 3 |pages= 301–6 |year= 2000 |pmid= 10606742 |doi=
*cite journal | author=Martínez-Maza R, Poyatos I, López-Corcuera B, "et al." |title=The role of N-glycosylation in transport to the plasma membrane and sorting of the neuronal glycine transporter GLYT2. |journal=J. Biol. Chem. |volume=276 |issue= 3 |pages= 2168–73 |year= 2001 |pmid= 11036075 |doi= 10.1074/jbc.M006774200
*cite journal | author=Geerlings A, Núñez E, Rodenstein L, "et al." |title=Glycine transporter isoforms show differential subcellular localization in PC12 cells. |journal=J. Neurochem. |volume=82 |issue= 1 |pages= 58–65 |year= 2002 |pmid= 12091465 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Mahendrasingam S, Wallam CA, Hackney CM |title=Two approaches to double post-embedding immunogold labeling of freeze-substituted tissue embedded in low temperature Lowicryl HM20 resin. |journal=Brain Res. Brain Res. Protoc. |volume=11 |issue= 2 |pages= 134–41 |year= 2003 |pmid= 12738009 |doi=
*cite journal | author=Baliova M, Betz H, Jursky F |title=Calpain-mediated proteolytic cleavage of the neuronal glycine transporter, GlyT2. |journal=J. Neurochem. |volume=88 |issue= 1 |pages= 227–32 |year= 2004 |pmid= 14675166 |doi=
*cite journal | author=Tsutsumi S, Kamata N, Vokes TJ, "et al." |title=The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD). |journal=Am. J. Hum. Genet. |volume=74 |issue= 6 |pages= 1255–61 |year= 2004 |pmid= 15124103 |doi= 10.1086/421527
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Jamra RA, Villela AW, Klein K, "et al." |title=No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia. |journal=Psychiatr. Genet. |volume=16 |issue= 3 |pages= 91 |year= 2006 |pmid= 16691125 |doi= 10.1097/01.ypg.0000199450.07786.ab
*cite journal | author=Rees MI, Harvey K, Pearce BR, "et al." |title=Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease. |journal=Nat. Genet. |volume=38 |issue= 7 |pages= 801–6 |year= 2006 |pmid= 16751771 |doi= 10.1038/ng1814
*cite journal | author=Eulenburg V, Becker K, Gomeza J, "et al." |title=Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia. |journal=Biochem. Biophys. Res. Commun. |volume=348 |issue= 2 |pages= 400–5 |year= 2006 |pmid= 16884688 |doi= 10.1016/j.bbrc.2006.07.080

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