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- accession：NM_001243475
- 基因别名：B9D1
- 基因描述：Homo sapiens B9 protein domain 1 (B9D1), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：444
- 翻译后氨基酸长度：147
- TranscriptVariant：This variant (3) is different on both the 5' and 3' ends, compared to variant 1. The resulting protein (isoform c) is shorter and with different 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
