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- 商品货号：G113035
- accession：NM_015681
- 基因别名：B9D1
- 基因描述：Homo sapiens B9 protein domain 1 (B9D1), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：615
- 翻译后氨基酸长度：204
- TranscriptVariant：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.
- 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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
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