人 CEP41 (NM_001257160) cDNA克隆

基本信息

Accession: NM_001257160
基因名称: CEP41
基因别名: JBTS15; TSGA14
基因描述: Homo sapiens centrosomal protein 41kDa (CEP41), transcript variant 4, mRNA.
种属: Human
CDS区长度: 165 (查看编码区序列)
翻译后氨基酸长度: 54 (查看氨基酸序列)
Transcript Variant: This variant (4) lacks multiple exons in the 3' coding region and has a novel 3' terminus, compared to variant 1, which results in an isoform (4; also known as short (S) type) which has a severely truncated and distinct C-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G167754 人 CEP41 (NM_001257160) 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 CEP41 (NM_018718) cDNA克隆 transcript variant 1
人 CEP41 (NM_001257158) cDNA克隆 transcript variant 2
人 CEP41 (NM_001257159) cDNA克隆 transcript variant 3
人 CEP41 (NM_001257160) cDNA克隆 transcript variant 4

基因简介

This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]

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