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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 [5]

Associated Conditions

Mutations in the KCNT1 gene has been shown to be a cause of Early Infantile Epileptic Encephalopathy. [6]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000107147Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000058740Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: KCNT1 potassium channel, subfamily T, member 1".
  6. ^ "OMIM: 614959". {{cite web}}: Missing or empty |url= (help)

Further reading

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