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- accession：NM_015560
- 基因别名：OPA1
- 基因描述：Homo sapiens optic atrophy 1 (autosomal dominant) (OPA1), transcript variant 1, mRNA.
- 载体：现货载体
- CDS区长度：2883
- 翻译后氨基酸长度：960
- TranscriptVariant：This variant (1) is the original transcript identified. It contains 29 exons and encodes an isoform (1) of 960 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
