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- accession：NM_001164720
- 基因别名：CC2D2A
- 基因描述：Homo sapiens coiled-coil and C2 domain containing 2A (CC2D2A), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：336
- 翻译后氨基酸长度：111
- TranscriptVariant：This variant (3) differs in the presence and absence of exons at its 3' end, compared to variant 1. The encoded isoform (c) has a distinct and significantly shorter C-terminus, compared to isoform a.
- 基因简介：This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
- 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
