This gene encodes a protein that is thought to be involved with centrosome function. Mutations in this gene have been associated with primary microcephaly (MCPH4). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]
人 CEP152 (NM_001194998) cDNA克隆
| Accession: | NM_001194998 |
|---|---|
| 基因名称: | CEP152 |
| 基因别名: | MCPH4; MCPH9; SCKL5 |
| 基因描述: | Homo sapiens centrosomal protein 152kDa (CEP152), transcript variant 1, mRNA. |
| 种属: | Human |
| CDS区长度: | 5133 (查看编码区序列) |
| 翻译后氨基酸长度: | 1710 (查看氨基酸序列) |
| Transcript Variant: | This variant (1) represents the longer variant and encodes the longer isoform (1). |
| 人 CEP152 (NM_001194998) cDNA克隆 | transcript variant 1 |
| 人 CEP152 (NM_014985) cDNA克隆 | transcript variant 2 |
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