- accession:NM_004403
- 基因别名:DFNA5
- 基因描述:Homo sapiens deafness, autosomal dominant 5 (DFNA5), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1491
- 翻译后氨基酸长度:496
- TranscriptVariant:This variant (1) represents the longest transcript and encodes the longer isoform (a). Variants 1 and 2 both encode 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]
- 载体信息:自有图片地址
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列