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人 WHSC1 (NM_133330) ORF克隆产品信息
订购信息
| 货号 | 种属 | 载体 | 描述 | 价格 | 周期 |
| QHO00036 | Human ORF | pMD19-T Simple Vector | Homo sapiens Wolf-Hirschhorn syndrome candidate 1 (WHSC1，MMSET，NSD2，REIIBP，TRX5，WHS),transcript variant 1, mRNANM_133330 1-2个工作日发货 已测序验证 | 5000 4000 | 现货 |
基本信息
| 基因名称： | WHSC1 |
| 基因别名： | FLJ23286; KIAA1090; MGC176638; MMSET; NSD2; REIIBP; TRX5; WHS |
| NCBI序列号： | NM_133330 |
| 基因描述： | Homo sapiens Wolf-Hirschhorn syndrome candidate 1 (WHSC1，MMSET，NSD2，REIIBP，TRX5，WHS),transcript variant 1, mRNA NM_133330 |
| 基因种属： | Human |
产品说明书
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载体信息
基因简介
This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences.
