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- accession：NM_001257159
- 基因别名：JBTS15; TSGA14
- 基因描述：Homo sapiens centrosomal protein 41kDa (CEP41), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：858
- 翻译后氨基酸长度：285
- TranscriptVariant：This variant (3) lacks two in-frame exons in the coding region, compared to variant 1, which results in a shorter isoform (3), compared to isoform 1.
- 基因简介：This gene encodes a centrosomal and microtubule-binding protein which is predicted to have two coiled-coil domains and a rhodanese domain. In human retinal pigment epithelial cells the protein localized to centrioles and cilia. Mutations in this gene have been associated with Joubert Syndrome 15; an autosomal recessive ciliopathy and neurological disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]
- 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
