人 B9D1 (NM_015681) cDNA克隆

基本信息

Accession: NM_015681
基因名称: B9D1
基因别名: B9; MKS9; EPPB9; MKSR1
基因描述: Homo sapiens B9 protein domain 1 (B9D1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 615 (查看编码区序列)
翻译后氨基酸长度: 204 (查看氨基酸序列)
Transcript Variant: This variant (2) uses different splicing at both ends, which results in the use of a different downstream start codon, compared to variant 1. The resulting protein (isoform b) has different N- and C-termini when it is compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G113035 人 B9D1 (NM_015681) 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 B9D1 (NM_001243473) cDNA克隆 transcript variant 1
人 B9D1 (NM_015681) cDNA克隆 transcript variant 2
人 B9D1 (NM_001243475) cDNA克隆 transcript variant 3

基因简介

This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Aug 2011]

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