人 ARL13B (NM_001174151) cDNA克隆

基本信息

Accession: NM_001174151
基因名称: ARL13B
基因别名: JBTS8; ARL2L1
基因描述: Homo sapiens ADP-ribosylation factor-like 13B (ARL13B), transcript variant 4, mRNA.
种属: Human
CDS区长度: 978 (查看编码区序列)
翻译后氨基酸长度: 325 (查看氨基酸序列)
Transcript Variant: 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.

订购信息

产品编号 产品名称 载体 规格 价格
G123439 人 ARL13B (NM_001174151) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 ARL13B (NM_182896) cDNA克隆 transcript variant 1
人 ARL13B (NM_144996) cDNA克隆 transcript variant 2
人 ARL13B (NM_001174150) cDNA克隆 transcript variant 3
人 ARL13B (NM_001174151) cDNA克隆 transcript variant 4

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]

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