| SLC6A5 | 
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| Identifiers | 
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| Aliases | SLC6A5, GLYT-2, GLYT2, HKPX3, NET1, Glycine transporter 2, solute carrier family 6 member 5 | 
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| External IDs | OMIM: 604159; MGI: 105090; HomoloGene: 37901; GeneCards: SLC6A5; OMA:SLC6A5 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 7 (mouse) | 
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 |  |  | Band | 7|7 B4 | Start | 49,559,894 bp | 
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 | End | 49,613,604 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | secondary oocyte
 testicle
 superior vestibular nucleus
 metencephalon
 Cerebellum
 spinal cord
 cerebellar cortex
 cerebellar hemisphere
 right hemisphere of cerebellum
 left testis
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 | | Top expressed in |  | medial vestibular nucleus
 pontine nuclei
 spinal cord
 Gray matter of spinal cord
 anterior horn of spinal cord
 deep cerebellar nuclei
 lumbar subsegment of spinal cord
 posterior horn of spinal cord
 gray matter layer of cerebellum
 neural layer of retina
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Sodium- and chloride-dependent glycine transporter 2, also known as glycine transporter 2 (GlyT2), is a protein that in humans is encoded by the SLC6A5 gene.
The glycine transporter 2 is a membrane protein which recaptures glycine, a major inhibitory transmitter in the spinal cord and brainstem.  GlyT2 is a specific marker of glycinergic neurons and a member of the Na+ and Cl−-coupled transporter family SLC6. Glycine uptake mediated by GlyT2 is electrogenic, coupled to three Na+ and one Cl− (i.e. two positive charges per glycine). In humans, GlyT2 is encoded by the SLC6A5 gene. Inactivation of GlyT2 in knockout mice is lethal during the second post-natal week as the absence of GlyT2 disrupts inhibitory transmission by reducing glycine release. Mutations in SLC6A5 gene are responsible for a presynaptic form of hyperekplexia, a genetic disease causing increased startle reflex. GlyT2 main physiological role is to recapture glycine released in the synaptic cleft and to maintain high glycine concentration in the presynaptic neuron. Therefore, chronic inhibition of GlyT2 will deplete intracellular storage of glycine and limit its accumulation in synaptic vesicles.