人 TBL1X (NM_001139467) cDNA克隆

Accession: NM_001139467
基因名称: TBL1X
基因别名: EBI; TBL1; SMAP55
基因描述: Homo sapiens transducin (beta)-like 1X-linked (TBL1X), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1581 (查看编码区序列)
翻译后氨基酸长度: 526 (查看氨基酸序列)
Transcript Variant: This variant (3) differs in the 5' UTR and lacks the alternate first coding exon compared to variant 1. The resulting isoform (b) is shorter at the N-terminus compared to isoform a. Variants 3 and 4 both encode isoform b.
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G119449 人 TBL1X (NM_001139467) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene has sequence similarity with members of the WD40 repeat-containing protein family. The WD40 group is a large family of proteins, which appear to have a regulatory function. It is believed that the WD40 repeats mediate protein-protein interactions and members of the family are involved in signal transduction, RNA processing, gene regulation, vesicular trafficking, cytoskeletal assembly and may play a role in the control of cytotypic differentiation. This encoded protein is found as a subunit in corepressor SMRT (silencing mediator for retinoid and thyroid receptors) complex along with histone deacetylase 3 protein. This gene is located adjacent to the ocular albinism gene and it is thought to be involved in the pathogenesis of the ocular albinism with late-onset sensorineural deafness phenotype. Four transcript variants encoding two different isoforms have been found for this gene. This gene is highly similar to the Y chromosome TBL1Y gene. [provided by RefSeq, Nov 2008]