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- accession：NM_001198543
- 基因别名：HYDIN
- 基因描述：Homo sapiens HYDIN, axonemal central pair apparatus protein (HYDIN), transcript variant 4, mRNA.
- 载体：现货载体
- CDS区长度：2823
- 翻译后氨基酸长度：940
- TranscriptVariant：This variant (4) differs in the 5' UTR and initiates translation at an alternate upstream start codon, compared to variant 1. This variant also differs in the 3' coding region and 3' UTR, compared to variant 1. The resulting isoform (d) has distinct N- and C-termini and is shorter than isoform a.
- 基因简介：This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]
- 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
