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- accession：NM_001083885
- 基因别名：DFNB31
- 基因描述：Homo sapiens deafness, autosomal recessive 31 (DFNB31), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1575
- 翻译后氨基酸长度：524
- TranscriptVariant：This variant (2) has multiple differences in the presence and absence of exons at its 5' end, compared to variant 1. These differences produce a unique 5' UTR and cause translation initiation at a downstream start codon, compared to variant 1. The encoded protein (isoform 2) is shorter than isoform 1.
- 基因简介：This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Mar 2010]
- 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
