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- accession：NM_001265594
- 基因别名：PLEKHG5
- 基因描述：Homo sapiens pleckstrin homology domain containing, family G (with RhoGef domain) member 5 (PLEKHG5), transcript variant 8, mRNA.
- 载体：现货载体
- CDS区长度：2793
- 翻译后氨基酸长度：930
- TranscriptVariant：This variant (8) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at an alternate start codon, and uses an alternate splice site in the 3' coding region which results in a frameshift compared to variant 1. The encoded protein (isoform f) is shorter and has distinct N- and C-termini compared to isoform b.
- 基因简介：This gene encodes a protein that activates the nuclear factor kappa B (NFKB1) signaling pathway. Mutations in this gene are associated with autosomal recessive distal spinal muscular atrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]
- 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
