KCNT1

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Potassium channel, subfamily T, member 1
Identifiers
Symbols KCNT1 ; EIEE14; ENFL5; KCa4.1; SLACK; bA100C15.2
External IDs OMIM608167 MGI1924627 HomoloGene11055 IUPHAR: KCa4.1 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:
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[edit]

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

See also[edit]

References[edit]

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

Further reading[edit]