• accession：NM_025136
• 基因别名：OPA3
• 基因描述：Homo sapiens optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) (OPA3), transcript variant 2, mRNA.
• 载体：现货载体
• CDS区长度：540
• 翻译后氨基酸长度：179
• TranscriptVariant：This variant (2) represents the longer transcript but encodes the shorter isoform (b).
• 基因简介：The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
• 规格：10ul 质粒

CDS区参考序列： 点击查看序列

ATGGTGGTGGGCGCGTTCCCTATGGCGAAGCTGCTATACTTGGGCATCCGGCAGGTCAGCAAGCCGCTTG
CCAACCGTATTAAGGAGGCCGCCCGCCGAAGCGAGTTCTTCAAGACCTATATCTGCCTCCCGCCGGCTCA
ACTGTATCACTGGGTGGAGATGCGGACCAAGATGCGCATCATGGGCTTCCGGGGCACGGTCATCAAGCCG
CTGAACGAGGAGGCGGCAGCTGAGCTGGGCGCAGAGCTGCTGGGCGAAGCCACCATCTTCATCGTGGGCG
GCGGCTGCCTAGTGCTGGAGTACTGGCGCCACCAGGCGCAGCAGCGCCACAAGGAGGAGGAGCAGCGTGC
TGCCTGGAACGCGCTGCGGGACGAGGTGGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCAGGCGCAGGTG
CAGGCGGCGCCGCCACAGGGCGCCCTGGAGGAACTGCGCACAGAGCTGCAAGAGGTGCGCGCCCAGCTCT
GCAATCCCGGCCGGTCCGCTTCCCACGCAGTGCCTGCGTCCAAGAAATAG

翻译后氨基酸参数序列： 点击查看序列

ATGGTGGTGGGCGCGTTCCCTATGGCGAAGCTGCTATACTTGGGCATCCGGCAGGTCAGCAAGCCGCTTG
CCAACCGTATTAAGGAGGCCGCCCGCCGAAGCGAGTTCTTCAAGACCTATATCTGCCTCCCGCCGGCTCA
ACTGTATCACTGGGTGGAGATGCGGACCAAGATGCGCATCATGGGCTTCCGGGGCACGGTCATCAAGCCG
CTGAACGAGGAGGCGGCAGCTGAGCTGGGCGCAGAGCTGCTGGGCGAAGCCACCATCTTCATCGTGGGCG
GCGGCTGCCTAGTGCTGGAGTACTGGCGCCACCAGGCGCAGCAGCGCCACAAGGAGGAGGAGCAGCGTGC
TGCCTGGAACGCGCTGCGGGACGAGGTGGGCCACCTGGCGCTGGCGCTGGAAGCGCTGCAGGCGCAGGTG
CAGGCGGCGCCGCCACAGGGCGCCCTGGAGGAACTGCGCACAGAGCTGCAAGAGGTGCGCGCCCAGCTCT
GCAATCCCGGCCGGTCCGCTTCCCACGCAGTGCCTGCGTCCAAGAAATAG