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- accession：NM_001278190
- 基因别名：TPM3
- 基因描述：Homo sapiens tropomyosin 3 (TPM3), transcript variant 8, mRNA.
- 载体：现货载体
- CDS区长度：684
- 翻译后氨基酸长度：227
- TranscriptVariant：This variant (8) lacks an alternate exon in the central coding region, but maintains the reading frame, compared to variant 2. The encoded isoform (8) is shorter than isoform 2.
- 基因简介：This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 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
