人 ZMYM3 (NM_201599) cDNA克隆

Accession: NM_201599
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 1, mRNA.
种属: Human
CDS区长度: 4113 (查看编码区序列)
翻译后氨基酸长度: 1370 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the predominant transcript. Variants 1 and 2 encode the same isoform (1).
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G111725 人 ZMYM3 (NM_201599) cDNA克隆 pDONR223 2ug质粒 点击询价

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]