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- accession：NM_001129731
- 基因别名：PLEKHG4
- 基因描述：Homo sapiens pleckstrin homology domain containing, family G (with RhoGef domain) member 4 (PLEKHG4), transcript variant 5, mRNA.
- 载体：现货载体
- CDS区长度：3333
- 翻译后氨基酸长度：1110
- TranscriptVariant：This variant (5) uses an alternative donor splice site at the 1st exon, and lacks the following coding exon compared to transcript variant 1. However, it maintains the reading frame and results in a shorter isoform (2) that is missing an internal protein segment compared to isoform 1.
- 基因简介：The protein encoded by this gene contains multiple domains suggestive of a role in intracellular signaling and cytoskeleton dynamics at the Golgi apparatus. Mutations in this gene are associated with spinocerebellar ataxia 16q22-linked. Several alternatively spliced transcript variants, differing only in the 5' UTR, or encoding a different isoform, have been found for this gene. [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
