人 SEPT9 (NM_001113494) cDNA克隆

基本信息

Accession: NM_001113494
基因名称: SEPT9
基因别名: MSF; MSF1; NAPB; SINT1; PNUTL4; SeptD1; AF17q25
基因描述: Homo sapiens septin 9 (SEPT9), transcript variant 6, mRNA.
种属: Human
CDS区长度: 1269 (查看编码区序列)
翻译后氨基酸长度: 422 (查看氨基酸序列)
Transcript Variant: This variant (6) lacks two 5' exons but has an alternate 5' exon, which results in a downstream AUG start codon, as compared to variant 1. The resulting isoform (e) has a shorter N-terminus,as compared to isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G107011 人 SEPT9 (NM_001113494) 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 SEPT9 (NM_001113491) cDNA克隆 transcript variant 1
人 SEPT9 (NM_001113493) cDNA克隆 transcript variant 2
人 SEPT9 (NM_006640) cDNA克隆 transcript variant 3
人 SEPT9 (NM_001113495) cDNA克隆 transcript variant 4
人 SEPT9 (NM_001113492) cDNA克隆 transcript variant 5
人 SEPT9 (NM_001113494) cDNA克隆 transcript variant 6
人 SEPT9 (NM_001113496) cDNA克隆 transcript variant 7

基因简介

This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2009]

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