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- accession：NM_031992
- 基因别名：EIF4H
- 基因描述：Homo sapiens eukaryotic translation initiation factor 4H (EIF4H), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：687
- 翻译后氨基酸长度：228
- TranscriptVariant：This variant (2) lacks an in-frame exon in the coding region, compared to variant 1. This variant encodes isoform 2 which is shorter, compared to isoform 1.
- 基因简介：This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants. [provided by RefSeq, Jul 2008]
- 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
