人 SLC26A7 (NM_001282357) cDNA克隆

基本信息

Accession: NM_001282357
基因名称: SLC26A7
基因别名: SUT2
基因描述: Homo sapiens solute carrier family 26 (anion exchanger), member 7 (SLC26A7), transcript variant 4, mRNA.
种属: Human
CDS区长度: 1068 (查看编码区序列)
翻译后氨基酸长度: 355 (查看氨基酸序列)
Transcript Variant: This variant (4) has multiple differences, compared to variant 3. This variant represents translation initiation at a downstream AUG; the 5'-most initiation codon, as used in variant 3, is associated with a truncated ORF that would render the transcript a candidate for nonsense-mediated decay (NMD). Leaky scanning may allow translation initiation at the downstream AUG to encode isoform c.

订购信息

产品编号 产品名称 载体 规格 价格
G123057 人 SLC26A7 (NM_001282357) 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 SLC26A7 (NM_052832) cDNA克隆 transcript variant 1
人 SLC26A7 (NM_134266) cDNA克隆 transcript variant 2
人 SLC26A7 (NM_001282356) cDNA克隆 transcript variant 3
人 SLC26A7 (NM_001282357) cDNA克隆 transcript variant 4

基因简介

This gene is one member of a family of sulfate/anion transporter genes. Family members are well conserved in gene structure and protein length yet have markedly different tissue expression patterns. This gene has abundant and specific expression in the kidney. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Aug 2013]

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