Gene: KCNT1 (potassium sodium-activated channel subfamily T member 1) Homo sapiens
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Symbol: KCNT1
Name: potassium sodium-activated channel subfamily T member 1
Description: Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a sodium-activated potassium channel subunit which is thought to function in ion conductance and developmental signaling pathways. Mutations in this gene cause the early-onset epileptic disorders, malignant migrating partial seizures of infancy and autosomal dominant nocturnal frontal lobe epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: bA100C15.2; EIEE14; ENFL5; FLJ41282; KCa4.1; OTTHUMP00000022558; OTTHUMP00000215618; OTTHUMP00000215619; OTTHUMP00000215620; OTTHUMP00000215622; OTTHUMP00000215624; potassium channel subfamily T member 1; potassium channel subunit (slack); potassium channel, sodium activated subfamily T, member 1; potassium channel, subfamily T, member 1; Sequence like a calcium-activated K+ channel; SLACK; Slo2.2
Orthologs:
Mus musculus (house mouse) : Kcnt1 (potassium channel, subfamily T, member 1)  MGI
Rattus norvegicus (Norway rat) : Kcnt1 (potassium sodium-activated channel subfamily T member 1)
Chinchilla lanigera (long-tailed chinchilla) : Kcnt1 (potassium sodium-activated channel subfamily T member 1)
Pan paniscus (bonobo/pygmy chimpanzee) : KCNT1 (potassium sodium-activated channel subfamily T member 1)
Canis lupus familiaris (dog) : KCNT1 (potassium sodium-activated channel subfamily T member 1)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Kcnt1 (potassium sodium-activated channel subfamily T member 1)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh389135,700,807 - 135,793,147 (+)NCBIGRCh38hg38GRCh38
GRCh379138,594,031 - 138,684,993 (+)NCBIGRCh37hg19GRCh37
Build 369137,733,859 - 137,824,813 (+)NCBINCBI36hg18NCBI36
Build 349135,819,982 - 135,904,199NCBI
Celera9109,111,863 - 109,202,929 (+)NCBI
Cytogenetic Map9q34.3NCBImapview
HuRef9108,055,583 - 108,146,760 (+)NCBI
CHM1_19138,742,378 - 138,833,497 (+)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

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Nomenclature History
 
More on KCNT1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
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RGD Object Information
RGD ID: 734382
Created: 2004-01-12
Species: Homo sapiens
Last Modified: 2017-06-13
Status: ACTIVE