人 CLN3 (NM_001286109) cDNA克隆

基本信息

Accession: NM_001286109
基因名称: CLN3
基因别名: BTS; JNCL
基因描述: Homo sapiens ceroid-lipofuscinosis, neuronal 3 (CLN3), transcript variant 5, mRNA.
种属: Human
CDS区长度: 1083 (查看编码区序列)
翻译后氨基酸长度: 360 (查看氨基酸序列)
Transcript Variant: This variant (5) differs in the 5' UTR and coding sequence, the 3' UTR, and lacks an alternate in-frame exon compared to variant 1. These differences cause translation initiation at a downstream AUG and result in an isoform (d) with a shorter N-terminus and missing an alternate internal segment compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G101924 人 CLN3 (NM_001286109) 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 CLN3 (NM_001042432) cDNA克隆 transcript variant 1
人 CLN3 (NM_000086) cDNA克隆 transcript variant 2
人 CLN3 (NM_001286104) cDNA克隆 transcript variant 3
人 CLN3 (NM_001286105) cDNA克隆 transcript variant 4
人 CLN3 (NM_001286109) cDNA克隆 transcript variant 5
人 CLN3 (NM_001286110) cDNA克隆 transcript variant 6

基因简介

This gene encodes a protein that is involved in lysosomal function. Mutations in this, as well as other neuronal ceroid-lipofuscinosis (CLN) genes, cause neurodegenerative diseases commonly known as Batten disease or collectively known as neuronal ceroid lipofuscinoses (NCLs). Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]

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