• accession：NM_183059
• 基因别名：RD3
• 基因描述：Homo sapiens retinal degeneration 3 (RD3), transcript variant 1, mRNA.
• 载体： 现货载体
• CDS区长度：588
• 翻译后氨基酸长度：195
• TranscriptVariant：This variant (1) represents the longer transcript. Both variants 1 and 2 encode the same protein.
• 基因简介：This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
• 载体信息：自有图片地址
• 规格：10ul 质粒

CDS区参考序列： 点击查看序列

ATGTCTCTCATCTCATGGCTTCGGTGGAACGAGGCCCCATCCCGGCTGTCCACCAGGAGCCCTGCTGAGATGGTGCTGGAGACGCTTATGATGGAGCTGACGGGGCAGATGCGAGAGGCTGAGAGGCAGCAGCGGGAGCGCAGCAATGCGGTCAGAAAGGTCTGCACCGGTGTGGACTACAGCTGGCTGGCCAGCACACCCCGGTCCACCTATGACCTCAGCCCCATTGAGCGGTTGCAGCTGGAAGATGTCTGCGTTAAGATCCACCCATCCTATTGTGGGCCTGCTATCCTCAGGTTCCGGCAGCTGCTGGCGGAGCAGGAGCCCGAGGTGCAGGAGGTGTCCCAGCTCTTCCGCTCGGTGCTGCAGGAGGTCCTGGAGAGGATGAAGCAGGAAGAGGAGGCCCACAAGCTGACGCGCCAGTGGAGCCTGCGGCCCCGCGGCAGCCTGGCCACCTTCAAGACCCGCGCGCGCATCTCGCCCTTCGCCAGCGACATCAGGACCATCTCCGAGGACGTGGAGCGGGACACACCGCCGCCACTGCGGTCCTGGAGCATGCCCGAATTCCGGGCGCCCAAAGCCGACTGA

翻译后氨基酸参数序列： 点击查看序列

ATGTCTCTCATCTCATGGCTTCGGTGGAACGAGGCCCCATCCCGGCTGTCCACCAGGAGCCCTGCTGAGATGGTGCTGGAGACGCTTATGATGGAGCTGACGGGGCAGATGCGAGAGGCTGAGAGGCAGCAGCGGGAGCGCAGCAATGCGGTCAGAAAGGTCTGCACCGGTGTGGACTACAGCTGGCTGGCCAGCACACCCCGGTCCACCTATGACCTCAGCCCCATTGAGCGGTTGCAGCTGGAAGATGTCTGCGTTAAGATCCACCCATCCTATTGTGGGCCTGCTATCCTCAGGTTCCGGCAGCTGCTGGCGGAGCAGGAGCCCGAGGTGCAGGAGGTGTCCCAGCTCTTCCGCTCGGTGCTGCAGGAGGTCCTGGAGAGGATGAAGCAGGAAGAGGAGGCCCACAAGCTGACGCGCCAGTGGAGCCTGCGGCCCCGCGGCAGCCTGGCCACCTTCAAGACCCGCGCGCGCATCTCGCCCTTCGCCAGCGACATCAGGACCATCTCCGAGGACGTGGAGCGGGACACACCGCCGCCACTGCGGTCCTGGAGCATGCCCGAATTCCGGGCGCCCAAAGCCGACTGA