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- accession：NM_001127897
- 基因别名：RPGRIP1L
- 基因描述：Homo sapiens RPGRIP1-like (RPGRIP1L), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：3708
- 翻译后氨基酸长度：1235
- TranscriptVariant：This variant (2) lacks two alternate in-frame exons compared to variant 1. The resulting isoform (b) has the same N- and C-termini but is shorter compared to isoform a.
- 基因简介：The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms 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
