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- accession：NM_015922
- 基因别名：NSDHL
- 基因描述：Homo sapiens NAD(P) dependent steroid dehydrogenase-like (NSDHL), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：1122
- 翻译后氨基酸长度：373
- TranscriptVariant：This variant (1) represents the more predominant transcript. Transcript variants 1 and 2 encode the same protein.
- 基因简介：The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq, Jul 2008]
- 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
