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- accession：NM_001281447
- 基因别名：GTF2IRD2
- 基因描述：Homo sapiens GTF2I repeat domain containing 2 (GTF2IRD2), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：327
- 翻译后氨基酸长度：108
- TranscriptVariant：This variant (2) lacks multiple 3' coding exons and its transcription extends past a splice site used in the variant 1, resulting in a distinct 3' coding region and 3' UTR. The encoded isoform (2) is shorter and has a distinct C-terminus, compared to isoform 1.
- 基因简介：This gene is one of several closely related genes on chromosome 7 encoding proteins containing helix-loop-helix motifs. These proteins may function as regulators of transcription. The encoded protein is unique in that its C-terminus is derived from CHARLIE8 transposable element sequence. This gene is located in a region of chromosome 7 that is deleted in Williams-Beuren syndrome, and loss of this locus may contribute to the cognitive phenotypes observed in this disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
