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This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. Protein function: Probably involved in the repair of mismatches in DNA. [The UniProt Consortium]
Keywords:
PMS1, PMSL1, PMS1 protein homolog 1, DNA mismatch repair protein PMS1, PMS1 Polyclonal Antibody
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