人 KMT2A (NM_001197104) cDNA克隆

Accession: NM_001197104
基因名称: KMT2A
基因别名: HRX; MLL; TRX1; ALL-1; CXXC7; HTRX1; MLL1A; WDSTS; MLL/GAS7; TET1-MLL
基因描述: Homo sapiens lysine (K)-specific methyltransferase 2A (KMT2A), transcript variant 1, mRNA.
种属: Human
CDS区长度: 11919 (查看编码区序列)
翻译后氨基酸长度: 3972 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longer transcript and encodes the longer isoform (1).
产品编号 产品名称 载体 规格 价格
G152418 人 KMT2A (NM_001197104) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a transcriptional coactivator that plays an essential role in regulating gene expression during early development and hematopoiesis. The encoded protein contains multiple conserved functional domains. One of these domains, the SET domain, is responsible for its histone H3 lysine 4 (H3K4) methyltransferase activity which mediates chromatin modifications associated with epigenetic transcriptional activation. This protein is processed by the enzyme Taspase 1 into two fragments, MLL-C and MLL-N. These fragments reassociate and further assemble into different multiprotein complexes that regulate the transcription of specific target genes, including many of the HOX genes. Multiple chromosomal translocations involving this gene are the cause of certain acute lymphoid leukemias and acute myeloid leukemias. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010]