人 MLXIPL (NM_032953) cDNA克隆

基本信息

Accession: NM_032953
基因名称: MLXIPL
基因别名: MIO; CHREBP; MONDOB; WBSCR14; WS-bHLH; bHLHd14
基因描述: Homo sapiens MLX interacting protein-like (MLXIPL), transcript variant 3, mRNA.
种属: Human
CDS区长度: 2553 (查看编码区序列)
翻译后氨基酸长度: 850 (查看氨基酸序列)
Transcript Variant: This variant (3) uses an alternate in-frame splice site in the coding region, compared to variant 1, resulting in a shorter protein (isoform gamma).

订购信息

产品编号 产品名称 载体 规格 价格
G153861 人 MLXIPL (NM_032953) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 MLXIPL (NM_032951) cDNA克隆 transcript variant 1
人 MLXIPL (NM_032952) cDNA克隆 transcript variant 2
人 MLXIPL (NM_032953) cDNA克隆 transcript variant 3
人 MLXIPL (NM_032954) cDNA克隆 transcript variant 4

基因简介

This gene encodes a basic helix-loop-helix leucine zipper transcription factor of the Myc/Max/Mad superfamily. This protein forms a heterodimeric complex and binds and activates, in a glucose-dependent manner, carbohydrate response element (ChoRE) motifs in the promoters of triglyceride synthesis genes. The gene is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. [provided by RefSeq, Jul 2008]

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