人 MSH6 (NM_001281494) cDNA克隆

Accession: NM_001281494
基因名称: MSH6
基因别名: GTBP; HSAP; p160; GTMBP; HNPCC5
基因描述: Homo sapiens mutS homolog 6 (MSH6), transcript variant 4, mRNA.
种属: Human
CDS区长度: 3177 (查看编码区序列)
翻译后氨基酸长度: 1058 (查看氨基酸序列)
Transcript Variant: This variant (4) contains an alternate exon in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a dowstream start codon compared to variant 1. The encoded isoform (3) is shorter and has a distinct N-terminus compared to isoform 1. Variants 3 and 4 encode the same protein (isoform 3).
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G114280 人 MSH6 (NM_001281494) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the DNA mismatch repair MutS family. In E. coli, the MutS protein helps in the recognition of mismatched nucleotides prior to their repair. A highly conserved region of approximately 150 aa, called the Walker-A adenine nucleotide binding motif, exists in MutS homologs. The encoded protein heterodimerizes with MSH2 to form a mismatch recognition complex that functions as a bidirectional molecular switch that exchanges ADP and ATP as DNA mismatches are bound and dissociated. Mutations in this gene may be associated with hereditary nonpolyposis colon cancer, colorectal cancer, and endometrial cancer. Transcripts variants encoding different isoforms have been described. [provided by RefSeq, Jul 2013]