人 OPA1 (NM_015560) cDNA克隆

基本信息

Accession: NM_015560
基因名称: OPA1
基因别名: NPG; NTG; MGM1; largeG
基因描述: Homo sapiens optic atrophy 1 (autosomal dominant) (OPA1), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2883 (查看编码区序列)
翻译后氨基酸长度: 960 (查看氨基酸序列)
Transcript Variant: This variant (1) is the original transcript identified. It contains 29 exons and encodes an isoform (1) of 960 aa.

订购信息

产品编号 产品名称 载体 规格 价格
G153152 人 OPA1 (NM_015560) 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 OPA1 (NM_015560) cDNA克隆 transcript variant 1
人 OPA1 (NM_130831) cDNA克隆 transcript variant 2
人 OPA1 (NM_130832) cDNA克隆 transcript variant 3
人 OPA1 (NM_130833) cDNA克隆 transcript variant 4
人 OPA1 (NM_130834) cDNA克隆 transcript variant 5
人 OPA1 (NM_130835) cDNA克隆 transcript variant 6
人 OPA1 (NM_130836) cDNA克隆 transcript variant 7
人 OPA1 (NM_130837) cDNA克隆 transcript variant 8

基因简介

This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

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