SLC6A5

Solute carrier family 6 (neurotransmitter transporter, glycine), member 5
Identifiers
Symbols	SLC6A5 ; GLYT2; NET1
External IDs	Template:OMIM5 Template:MGI HomoloGene: 37901
Gene ontology Molecular function Template:GNF GO Template:GNF GO Template:GNF GO Cellular component Template:GNF GO Template:GNF GO Biological process Template:GNF GO Template:GNF GO
RNA expression pattern
File:PBB GE SLC6A5 210810 s at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Solute carrier family 6 (neurotransmitter transporter, glycine), member 5, also known as SLC6A5, is a human gene.

See also

• Sodium:neurotransmitter symporter
• Solute carrier family

Further reading

• López-Corcuera B, Aragón C, Geerlings A (2002). "Regulation of glycine transporters". Biochem. Soc. Trans. 29 (Pt 6): 742–5. PMID 11709067.CS1 maint: Multiple names: authors list (link)
• Morrow JA, Collie IT, Dunbar DR; et al. (1998). "Molecular cloning and functional expression of the human glycine transporter GlyT2 and chromosomal localisation of the gene in the human genome". FEBS Lett. 439 (3): 334–40. PMID 9845349.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gallagher MJ, Burgess LH, Brunden KR (1999). "Characterization of multiple forms of the human glycine transporter type-2". Brain Res. Mol. Brain Res. 70 (1): 101–15. PMID 10381548.CS1 maint: Multiple names: authors list (link)
• Evans J, Herdon H, Cairns W; et al. (2000). "Cloning, functional characterisation and population analysis of a variant form of the human glycine type 2 transporter". FEBS Lett. 463 (3): 301–6. PMID 10606742.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Martínez-Maza R, Poyatos I, López-Corcuera B; et al. (2001). "The role of N-glycosylation in transport to the plasma membrane and sorting of the neuronal glycine transporter GLYT2". J. Biol. Chem. 276 (3): 2168–73. doi:10.1074/jbc.M006774200. PMID 11036075.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Geerlings A, Núñez E, Rodenstein L; et al. (2002). "Glycine transporter isoforms show differential subcellular localization in PC12 cells". J. Neurochem. 82 (1): 58–65. PMID 12091465.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Mahendrasingam S, Wallam CA, Hackney CM (2003). "Two approaches to double post-embedding immunogold labeling of freeze-substituted tissue embedded in low temperature Lowicryl HM20 resin". Brain Res. Brain Res. Protoc. 11 (2): 134–41. PMID 12738009.CS1 maint: Multiple names: authors list (link)
• Baliova M, Betz H, Jursky F (2004). "Calpain-mediated proteolytic cleavage of the neuronal glycine transporter, GlyT2". J. Neurochem. 88 (1): 227–32. PMID 14675166.CS1 maint: Multiple names: authors list (link)
• Tsutsumi S, Kamata N, Vokes TJ; et al. (2004). "The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD)". Am. J. Hum. Genet. 74 (6): 1255–61. doi:10.1086/421527. PMID 15124103.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Jamra RA, Villela AW, Klein K; et al. (2006). "No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia". Psychiatr. Genet. 16 (3): 91. doi:10.1097/01.ypg.0000199450.07786.ab. PMID 16691125.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Rees MI, Harvey K, Pearce BR; et al. (2006). "Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease". Nat. Genet. 38 (7): 801–6. doi:10.1038/ng1814. PMID 16751771.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Eulenburg V, Becker K, Gomeza J; et al. (2006). "Mutations within the human GLYT2 (SLC6A5) gene associated with hyperekplexia". Biochem. Biophys. Res. Commun. 348 (2): 400–5. doi:10.1016/j.bbrc.2006.07.080. PMID 16884688.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)