This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
人 DCAF17 (NM_025000) cDNA克隆
| Accession: | NM_025000 |
|---|---|
| 基因名称: | DCAF17 |
| 基因别名: | C2orf37 |
| 基因描述: | Homo sapiens DDB1 and CUL4 associated factor 17 (DCAF17), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 1563 (查看编码区序列) |
| 翻译后氨基酸长度: | 520 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) represents the longest transcript and encodes the longer isoform (1). |
| 人 DCAF17 (NM_025000) cDNA克隆 | transcript variant 1 |
| 人 DCAF17 (NM_001164821) cDNA克隆 | transcript variant 2 |
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