人 ST3GAL3 (NM_001270464) cDNA克隆

基本信息

Accession: NM_001270464
基因名称: ST3GAL3
基因别名: ST3N; MRT12; SIAT6; EIEE15; ST3GALII; ST3GalIII
基因描述: Homo sapiens ST3 beta-galactoside alpha-2,3-sialyltransferase 3 (ST3GAL3), transcript variant 16, mRNA.
种属: Human
CDS区长度: 561 (查看编码区序列)
翻译后氨基酸长度: 186 (查看氨基酸序列)
Transcript Variant: This variant (16) uses an alternate in-frame splice site in the 5' coding region and lacks five alternate in-frame exon compared to variant 1. The resulting isoform (p, also called C5) is shorter compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G116653 人 ST3GAL3 (NM_001270464) 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 ST3GAL3 (NM_174963) cDNA克隆 transcript variant 1
人 ST3GAL3 (NM_006279) cDNA克隆 transcript variant 10
人 ST3GAL3 (NM_001270459) cDNA克隆 transcript variant 11
人 ST3GAL3 (NM_001270460) cDNA克隆 transcript variant 12
人 ST3GAL3 (NM_001270461) cDNA克隆 transcript variant 13
人 ST3GAL3 (NM_001270462) cDNA克隆 transcript variant 14
人 ST3GAL3 (NM_001270463) cDNA克隆 transcript variant 15
人 ST3GAL3 (NM_001270464) cDNA克隆 transcript variant 16
人 ST3GAL3 (NM_001270465) cDNA克隆 transcript variant 17
人 ST3GAL3 (NM_001270466) cDNA克隆 transcript variant 18
人 ST3GAL3 (NM_174964) cDNA克隆 transcript variant 2
人 ST3GAL3 (NM_174965) cDNA克隆 transcript variant 3
人 ST3GAL3 (NM_174966) cDNA克隆 transcript variant 4
人 ST3GAL3 (NM_174967) cDNA克隆 transcript variant 5
人 ST3GAL3 (NM_174968) cDNA克隆 transcript variant 6
人 ST3GAL3 (NM_174969) cDNA克隆 transcript variant 7
人 ST3GAL3 (NM_174970) cDNA克隆 transcript variant 8
人 ST3GAL3 (NM_174971) cDNA克隆 transcript variant 9

基因简介

The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with autosomal recessive nonsymdromic mental retardation-12 (MRT12). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2012]

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