KCNT1

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KCNT1
Identifiers
AliasesKCNT1, EIEE14, ENFL5, KCa4.1, SLACK, bA100C15.2, Slo2.2, potassium sodium-activated channel subfamily T member 1
External IDsOMIM: 608167 MGI: 1924627 HomoloGene: 11055 GeneCards: KCNT1
Gene location (Human)
Chromosome 9 (human)
Chr.Chromosome 9 (human)[1]
Chromosome 9 (human)
Genomic location for KCNT1
Genomic location for KCNT1
Band9q34.3Start135,702,185 bp[1]
End135,795,508 bp[1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001272003
NM_020822

NM_001145403
NM_175462
NM_001302351

RefSeq (protein)

NP_001258932
NP_065873

NP_001138875
NP_001289280
NP_780671

Location (UCSC)Chr 9: 135.7 – 135.8 MbChr 2: 25.86 – 25.92 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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[edit]

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

See also[edit]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000107147 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000058740 - Ensembl, 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". Missing or empty |url= (help)

Further reading[edit]