人 WHSC1 (NM_133334) cDNA克隆

Accession: NM_133334
基因名称: WHSC1
基因别名: WHS; NSD2; TRX5; MMSET; REIIBP
基因描述: Homo sapiens Wolf-Hirschhorn syndrome candidate 1 (WHSC1), transcript variant 7, mRNA.
种属: Human
CDS区长度: 1944 (查看编码区序列)
翻译后氨基酸长度: 647 (查看氨基酸序列)
Transcript Variant: This variant (7) is missing most of the exons from the 3' end compared to variant 1. It has a different 3' UTR and encodes a shorter isoform (3) with a different C-terminus compared to isoform 1.
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G163969 人 WHSC1 (NM_133334) cDNA克隆 pDONR223 2ug质粒 点击询价

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. [provided by RefSeq, Jul 2008]