人 MAPT (NM_016835) cDNA克隆

基本信息

Accession: NM_016835
基因名称: MAPT
基因别名: TAU; MSTD; PPND; DDPAC; MAPTL; MTBT1; MTBT2; FTDP-17
基因描述: Homo sapiens microtubule-associated protein tau (MAPT), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2277 (查看编码区序列)
翻译后氨基酸长度: 758 (查看氨基酸序列)
Transcript Variant: This variant (1) lacks one internal coding exons, as compared to variant 6. The reading frame is not affected, and the resulting isoform (1) has identical N- and C-termini but lacks one segment, as compared to isoform 6.

订购信息

产品编号 产品名称 载体 规格 价格
G124039 人 MAPT (NM_016835) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 MAPT (NM_016835) cDNA克隆 transcript variant 1
人 MAPT (NM_005910) cDNA克隆 transcript variant 2
人 MAPT (NM_016834) cDNA克隆 transcript variant 3
人 MAPT (NM_016841) cDNA克隆 transcript variant 4
人 MAPT (NM_001123067) cDNA克隆 transcript variant 5
人 MAPT (NM_001123066) cDNA克隆 transcript variant 6
人 MAPT (NM_001203251) cDNA克隆 transcript variant 7
人 MAPT (NM_001203252) cDNA克隆 transcript variant 8

基因简介

This gene encodes the microtubule-associated protein tau (MAPT) whose transcript undergoes complex, regulated alternative splicing, giving rise to several mRNA species. MAPT transcripts are differentially expressed in the nervous system, depending on stage of neuronal maturation and neuron type. MAPT gene mutations have been associated with several neurodegenerative disorders such as Alzheimer's disease, Pick's disease, frontotemporal dementia, cortico-basal degeneration and progressive supranuclear palsy. [provided by RefSeq, Jul 2008]

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