人 BTBD9 (NM_152733) cDNA克隆

基本信息

Accession: NM_152733
基因名称: BTBD9
基因别名: dJ322I12.1
基因描述: Homo sapiens BTB (POZ) domain containing 9 (BTBD9), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1635 (查看编码区序列)
翻译后氨基酸长度: 544 (查看氨基酸序列)
Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (b) is shorter than isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G124395 人 BTBD9 (NM_152733) 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 BTBD9 (NM_052893) cDNA克隆 transcript variant 1
人 BTBD9 (NM_001099272) cDNA克隆 transcript variant 2
人 BTBD9 (NM_152733) cDNA克隆 transcript variant 3
人 BTBD9 (NM_001172418) cDNA克隆 transcript variant 4

基因简介

This locus encodes a BTB/POZ domain-containing protein. This domain is known to be involved in protein-protein interactions. Polymorphisms at this locus have been reported to be associated with susceptibility to Restless Legs Syndrome and may also be associated with Tourette Syndrome. Alternatively spliced transcript variants have been described. [provided by RefSeq, Aug 2011]

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