人 ST7 (NM_018412) cDNA克隆

基本信息

Accession: NM_018412
基因名称: ST7
基因别名: HELG; RAY1; SEN4; TSG7; ETS7q; FAM4A; FAM4A1
基因描述: Homo sapiens suppression of tumorigenicity 7 (ST7), transcript variant a, mRNA.
种属: Human
CDS区长度: 1665 (查看编码区序列)
翻译后氨基酸长度: 554 (查看氨基酸序列)
Transcript Variant: This variant (a) lacks an alternate internal exon and contains an alternate 3' coding exon and 3'UTR, as compared to variant b. The resulting isoform (a) is shorter and has a distinct C-terminus, compared to isoform b.

订购信息

产品编号 产品名称 载体 规格 价格
G119065 人 ST7 (NM_018412) 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 ST7 (NM_018412) cDNA克隆 transcript variant a
人 ST7 (NM_021908) cDNA克隆 transcript variant b

基因简介

The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]

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