人 CACNB2 (NM_001167945) cDNA克隆

基本信息

Accession: NM_001167945
基因名称: CACNB2
基因别名: MYSB; CAVB2; CACNLB2
基因描述: Homo sapiens calcium channel, voltage-dependent, beta 2 subunit (CACNB2), transcript variant 9, mRNA.
种属: Human
CDS区长度: 1785 (查看编码区序列)
翻译后氨基酸长度: 594 (查看氨基酸序列)
Transcript Variant: This variant (9) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, and has multiple coding region differences compared to variant 1. The encoded isoform (9) has a distinct N-terminus and is shorter than isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G165060 人 CACNB2 (NM_001167945) 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 CACNB2 (NM_000724) cDNA克隆 transcript variant 1
人 CACNB2 (NM_201596) cDNA克隆 transcript variant 2
人 CACNB2 (NM_201590) cDNA克隆 transcript variant 3
人 CACNB2 (NM_201597) cDNA克隆 transcript variant 4
人 CACNB2 (NM_201593) cDNA克隆 transcript variant 5
人 CACNB2 (NM_201571) cDNA克隆 transcript variant 6
人 CACNB2 (NM_201570) cDNA克隆 transcript variant 7
人 CACNB2 (NM_201572) cDNA克隆 transcript variant 8
人 CACNB2 (NM_001167945) cDNA克隆 transcript variant 9

基因简介

This gene encodes a subunit of a voltage-dependent calcium channel protein that is a member of the voltage-gated calcium channel superfamily. The gene product was originally identified as an antigen target in Lambert-Eaton myasthenic syndrome, an autoimmune disorder. Mutations in this gene are associated with Brugada syndrome. Alternatively spliced variants encoding different isoforms have been described. [provided by RefSeq, Feb 2013]

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