| SLC12A5 | 
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| Identifiers | 
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| Aliases | SLC12A5, KCC2, Chloride potassium symporter 5, EIEE34, EIG14, hKCC2, solute carrier family 12 member 5, DEE34 | 
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| External IDs | OMIM: 606726; MGI: 1862037; HomoloGene: 10665; GeneCards: SLC12A5; OMA:SLC12A5 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 2 (mouse) | 
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 |  |  | Band | 2|2 H3 | Start | 164,802,722 bp | 
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 | End | 164,841,651 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | right hemisphere of cerebellum
 lateral nuclear group of thalamus
 Brodmann area 23
 Brodmann area 10
 primary visual cortex
 dorsolateral prefrontal cortex
 Brodmann area 9
 frontal pole
 orbitofrontal cortex
 superior frontal gyrus
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 | | Top expressed in |  | dorsal tegmental nucleus
 anterior amygdaloid area
 medial geniculate nucleus
 globus pallidus
 lateral hypothalamus
 subiculum
 olfactory tubercle
 paraventricular nucleus of hypothalamus
 medial dorsal nucleus
 dorsomedial hypothalamic nucleus
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Potassium-chloride transporter member 5 (aka: KCC2 and SLC12A5) is a neuron-specific chloride potassium symporter responsible for establishing the chloride ion gradient in neurons through the maintenance of low intracellular chloride concentrations. It is a critical mediator of synaptic inhibition, cellular protection against excitotoxicity and may also act as a modulator of neuroplasticity. Potassium-chloride transporter member 5 is also known by the names: KCC2 (potassium chloride cotransporter 2) for its ionic substrates, and SLC12A5 for its genetic origin from the SLC12A5 gene in humans.
Animals with reduced expression of this transporter exhibit severe motor deficits, epileptiform activity, and spasticity. KCC2 knockout animals, in which KCC2 is completely absent, die postnatally due to respiratory failure.