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KCNT1

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Identifiers
SymbolsKCNT1 ; EIEE14; ENFL5; KCa4.1; SLACK; bA100C15.2
External IDsOMIM608167 MGI1924627 HomoloGene11055 IUPHAR: 385 GeneCards: KCNT1 Gene
Orthologs
SpeciesHumanMouse
Entrez57582227632
EnsemblENSG00000107147ENSMUSG00000058740
UniProtQ5JUK3Q6ZPR4
RefSeq (mRNA)NM_001272003NM_001145403
RefSeq (protein)NP_001258932NP_001138875
Location (UCSC)Chr 9:
138.59 – 138.68 Mb
Chr 2:
25.86 – 25.92 Mb
PubMed search[1][2]

Potassium channel subfamily T, member 1, also known as KCNT1 is a human gene that encodes the KCa4.1 protein. KCa4.1 is a member of the calcium-activated potassium channel protein family [1]

Associated Conditions

Mutations in the KCNT1 gene has been shown to be a cause of Early Infantile Epileptic Encephalopathy. [2]

See also

References

  1. "Entrez Gene: KCNT1 potassium channel, subfamily T, member 1". 
  2. "OMIM: 614959". 

Further reading

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