Chloride potassium symporter 5

SLC12A5
Identifiers
AliasesSLC12A5, KCC2, Chloride potassium symporter 5, EIEE34, EIG14, hKCC2, solute carrier family 12 member 5, DEE34
External IDsOMIM: 606726; MGI: 1862037; HomoloGene: 10665; GeneCards: SLC12A5; OMA:SLC12A5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

57468

57138

Ensembl

ENSG00000124140

ENSMUSG00000017740

UniProt

Q9H2X9

Q91V14

RefSeq (mRNA)

NM_020708
NM_001134771

NM_020333
NM_001355480
NM_001355481

RefSeq (protein)

NP_001128243
NP_065759

NP_065066
NP_001342409
NP_001342410

Location (UCSC)Chr 20: 46.02 – 46.06 MbChr 2: 164.8 – 164.84 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

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.