This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and mental retardation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011]
人 WDR62 (NM_001083961) cDNA克隆
| Accession: | NM_001083961 |
|---|---|
| 基因名称: | WDR62 |
| 基因别名: | MCPH2; C19orf14 |
| 基因描述: | Homo sapiens WD repeat domain 62 (WDR62), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 4572 (查看编码区序列) |
| 翻译后氨基酸长度: | 1523 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) represents the longer transcript and encodes the longer isoform (1). |
| 人 WDR62 (NM_001083961) cDNA克隆 | transcript variant 1 |
| 人 WDR62 (NM_173636) cDNA克隆 | transcript variant 2 |
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