人 ZMYM3 (NM_001171162) cDNA克隆

基本信息

Accession: NM_001171162
基因名称: ZMYM3
基因别名: MYM; XFIM; ZNF261; DXS6673E; ZNF198L2
基因描述: Homo sapiens zinc finger, MYM-type 3 (ZMYM3), transcript variant 3, mRNA.
种属: Human
CDS区长度: 4077 (查看编码区序列)
翻译后氨基酸长度: 1358 (查看氨基酸序列)
Transcript Variant: This variant (3) contains an alternate 5' non-coding exon, and uses an alternate in-frame donor splice site at an internal coding exon compared to variant 1. This results in a shorter isoform (2) missing a 12 aa protein segment compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G111722 人 ZMYM3 (NM_001171162) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 ZMYM3 (NM_201599) cDNA克隆 transcript variant 1
人 ZMYM3 (NM_005096) cDNA克隆 transcript variant 2
人 ZMYM3 (NM_001171162) cDNA克隆 transcript variant 3
人 ZMYM3 (NM_001171163) cDNA克隆 transcript variant 4

基因简介

This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked mental retardation. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010]

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