人 DNM1L (NM_005690) cDNA克隆

基本信息

Accession: NM_005690
基因名称: DNM1L
基因别名: DLP1; DRP1; DVLP; EMPF; DYMPLE; HDYNIV
基因描述: Homo sapiens dynamin 1-like (DNM1L), transcript variant 3, mRNA.
种属: Human
CDS区长度: 2100 (查看编码区序列)
翻译后氨基酸长度: 699 (查看氨基酸序列)
Transcript Variant: This variant (3) lacks two consecutive in-frame exons in the 3' coding region, compared to variant 1. The encoded isoform (3) is shorter, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G112716 人 DNM1L (NM_005690) 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 DNM1L (NM_012062) cDNA克隆 transcript variant 1
人 DNM1L (NM_012063) cDNA克隆 transcript variant 2
人 DNM1L (NM_005690) cDNA克隆 transcript variant 3
人 DNM1L (NM_001278463) cDNA克隆 transcript variant 4
人 DNM1L (NM_001278464) cDNA克隆 transcript variant 5
人 DNM1L (NM_001278465) cDNA克隆 transcript variant 6
人 DNM1L (NM_001278466) cDNA克隆 transcript variant 7

基因简介

This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]

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