This gene a protein plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]
人 C21orf59 (NM_021254) cDNA克隆
| Accession: | NM_021254 |
|---|---|
| 基因名称: | C21orf59 |
| 基因别名: | FBB18; CILD26; C21orf48 |
| 基因描述: | Homo sapiens chromosome 21 open reading frame 59 (C21orf59), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 873 (查看编码区序列) |
| 翻译后氨基酸长度: | 290 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) represents the longer transcript and encodes the functional protein. |
| 人 C21orf59 (NM_021254) cDNA克隆 | transcript variant 1 |
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