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- accession：NM_182896
- 基因别名：ARL13B
- 基因描述：Homo sapiens ADP-ribosylation factor-like 13B (ARL13B), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：1287
- 翻译后氨基酸长度：428
- TranscriptVariant：This variant (1) encodes the longest isoform (1). Both variants 1 and 2 encode the same isoform (1).
- 基因简介：This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
- 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
