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- accession：NM_001174151
- 基因别名：ARL13B
- 基因描述：Homo sapiens ADP-ribosylation factor-like 13B (ARL13B), transcript variant 4, mRNA.
- 载体：现货载体
- CDS区长度：978
- 翻译后氨基酸长度：325
- TranscriptVariant：This variant (4) differs in the 3' UTR, lacks an in-frame exon in the 5' coding region and uses a downstream start codon, compared to variant 1. The encoded isoform 3 has a shorter N-terminus, compared to 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
