人 KCNT1 (NM_001272003) cDNA克隆

Accession: NM_001272003
基因名称: KCNT1
基因别名: ENFL5; SLACK; EIEE14; KCa4.1; bA100C15.2
基因描述: Homo sapiens potassium channel, subfamily T, member 1 (KCNT1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 3636 (查看编码区序列)
翻译后氨基酸长度: 1211 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks an alternate exon in the 5' coding region, uses an alternate splice site in the 5' region and contains an additional exon in the 3' coding region, compared to variant 1. The encoded isoform (2) is shorter than isoform 1.
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G156572 人 KCNT1 (NM_001272003) cDNA克隆 pDONR223 2ug质粒 点击询价

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]