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- accession：NM_001127454
- 基因别名：DFNA5
- 基因描述：Homo sapiens deafness, autosomal dominant 5 (DFNA5), transcript variant 3, mRNA.
- 载体：现货载体
- CDS区长度：999
- 翻译后氨基酸长度：332
- TranscriptVariant：This variant (3) lacks an alternate exon compared to variant 1, resulting in an isoform (b) that uses a downstream start site compared to isoform a.
- 基因简介：Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
- 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
