KCNT1

Potassium channel, sodium activated subfamily T, member 1
Identifiers
Symbols KCNT1 ; EIEE14; ENFL5; KCa4.1; SLACK; Slo2.2; bA100C15.2
External IDs OMIM: 608167 MGI: 1924627 HomoloGene: 11055 IUPHAR: 385 GeneCards: KCNT1 Gene
Orthologs
Species Human Mouse
Entrez 57582 227632
Ensembl ENSG00000107147 ENSMUSG00000058740
UniProt Q5JUK3 Q6ZPR4
RefSeq (mRNA) NM_001272003 NM_001145403
RefSeq (protein) NP_001258932 NP_001138875
Location (UCSC) Chr 9:
135.7 – 135.8 Mb
Chr 2:
25.86 – 25.92 Mb
PubMed search

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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