Homo sapiens Gene: KCNT1 | |||||||
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Summary | |||||||
InnateDB Gene | IDBG-92102.6 | ||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||
Gene Symbol | KCNT1 | ||||||
Gene Name | potassium channel, subfamily T, member 1 | ||||||
Synonyms | |||||||
Species | Homo sapiens | ||||||
Ensembl Gene | ENSG00000107147 | ||||||
Encoded Proteins |
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
potassium channel, subfamily T, member 1
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Protein Structure | |||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||
Entrez Gene | |||||||
Summary |
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] |
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Gene Information | |||||||
Type | Protein coding | ||||||
Genomic Location | Chromosome 9:135702185-135793150 | ||||||
Strand | Forward strand | ||||||
Band | q34.3 | ||||||
Transcripts | |||||||
Interactions | |||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Cross-References | |||||||
SwissProt | |||||||
TrEMBL | |||||||
UniProt Splice Variant | |||||||
Entrez Gene | |||||||
UniGene | Hs.104950 | ||||||
RefSeq | NM_001272003 NM_020822 XM_006717193 XM_006717194 | ||||||
HUGO | |||||||
OMIM | |||||||
CCDS | CCDS35175 CCDS65188 | ||||||
HPRD | |||||||
IMGT | |||||||
EMBL | |||||||
GenPept | |||||||
RNA Seq Atlas | |||||||