人 MLH1 (NM_001258274) cDNA克隆

Accession: NM_001258274
基因名称: MLH1
基因别名: FCC2; COCA2; HNPCC; hMLH1; HNPCC2
基因描述: Homo sapiens mutL homolog 1 (MLH1), transcript variant 7, mRNA.
种属: Human
CDS区长度: 1548 (查看编码区序列)
翻译后氨基酸长度: 515 (查看氨基酸序列)
Transcript Variant: This variant (7) differs in the 5' UTR and contains an alternate exon compared to variant 1, that causes a frameshift. The resulting isoform (3) is shorter at the N-terminus compared to isoform 1. Variants 3, 4, 6, and 7 all encode the same isoform (3).
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G102531 人 MLH1 (NM_001258274) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). It is a human homolog of the E. coli DNA mismatch repair gene mutL, consistent with the characteristic alterations in microsatellite sequences (RER+phenotype) found in HNPCC. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described, but their full-length natures have not been determined.[provided by RefSeq, Nov 2009]