人 GTF2I (NM_001280800) cDNA克隆

基本信息

Accession: NM_001280800
基因名称: GTF2I
基因别名: WBS; DIWS; SPIN; IB291; BAP135; BTKAP1; TFII-I; WBSCR6; GTFII-I
基因描述: Homo sapiens general transcription factor IIi (GTF2I), transcript variant 6, mRNA.
种属: Human
CDS区长度: 825 (查看编码区序列)
翻译后氨基酸长度: 274 (查看氨基酸序列)
Transcript Variant: This variant (6) lacks multiple coding exons and its transcription extends past a splice site used in variant 1, resulting in a distinct 3' coding region and 3' UTR. The encoded isoform (6) is shorter and has a distinct C-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G146962 人 GTF2I (NM_001280800) 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 GTF2I (NM_032999) cDNA克隆 transcript variant 1
人 GTF2I (NM_033000) cDNA克隆 transcript variant 2
人 GTF2I (NM_033001) cDNA克隆 transcript variant 3
人 GTF2I (NM_001518) cDNA克隆 transcript variant 4
人 GTF2I (NM_001163636) cDNA克隆 transcript variant 5
人 GTF2I (NM_001280800) cDNA克隆 transcript variant 6

基因简介

This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013]

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