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- accession：NM_144596
- 基因别名：TTC8
- 基因描述：Homo sapiens tetratricopeptide repeat domain 8 (TTC8), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：1548
- 翻译后氨基酸长度：515
- TranscriptVariant：This variant (1) represents the longest transcript and encodes the longest isoform (A). Variants lacking the second exon of this transcript have been associated with nonsyndromic retinitis pigmentosa.
- 基因简介：This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. Alternate transcriptional splice variants have been characterized. [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
