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- accession：NM_130836
- 基因别名：OPA1
- 基因描述：Homo sapiens optic atrophy 1 (autosomal dominant) (OPA1), transcript variant 7, mRNA.
- 载体：现货载体
- CDS区长度：2994
- 翻译后氨基酸长度：997
- TranscriptVariant：This variant (7) contains an additional exon 5b, compared to transcript variant 1. It however, maintains the same reading frame and encodes an isoform (7) of 997 aa.
- 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]
- 规格：10ul 质粒
CDS区参考序列： 点击查看序列翻译后氨基酸参数序列： 点击查看序列
