人 TTC8 (NM_198310) cDNA克隆

Accession: NM_198310
基因名称: TTC8
基因别名: BBS8; RP51
基因描述: Homo sapiens tetratricopeptide repeat domain 8 (TTC8), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1428 (查看编码区序列)
翻译后氨基酸长度: 475 (查看氨基酸序列)
Transcript Variant: This variant (3) lacks two in-frame exons, compared to variant 1, resulting in a shorter protein (isoform C), as compared to isoform A.
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G112054 人 TTC8 (NM_198310) cDNA克隆 pDONR223 2ug质粒 点击询价

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]