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- accession：NM_178335
- 基因别名：CCDC50
- 基因描述：Homo sapiens coiled-coil domain containing 50 (CCDC50), transcript variant 2, mRNA.
- 载体：现货载体
- CDS区长度：1449
- 翻译后氨基酸长度：482
- TranscriptVariant：This variant (2) represents the longer transcript and encodes the long isoform.
- 基因简介：This gene encodes a soluble, cytoplasmic, tyrosine-phosphorylated protein with multiple ubiquitin-interacting domains. Mutations in this gene cause nonsyndromic, postlingual, progressive sensorineural DFNA44 hearing loss. In mouse, the protein is expressed in the inner ear during development and postnatal maturation and associates with microtubule-based structures. This protein may also function as a negative regulator of NF-kB signaling and as an effector of epidermal growth factor (EGF)-mediated cell signaling. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 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
