The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
人 ZNF778 (NM_001201407) cDNA克隆
| Accession: | NM_001201407 |
|---|---|
| 基因名称: | ZNF778 |
| 基因描述: | Homo sapiens zinc finger protein 778 (ZNF778), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 2274 (查看编码区序列) |
| 翻译后氨基酸长度: | 757 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) encodes the longer isoform (1). |
| 人 ZNF778 (NM_001201407) cDNA克隆 | transcript variant 1 |
| 人 ZNF778 (NM_182531) cDNA克隆 | transcript variant 2 |
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