6 articles
MLH1
MLH1, or mutL homolog 1, is a human gene on chromosome 3 whose protein repairs DNA replication errors; inherited variants cause Lynch syndrome, a hereditary cancer predisposition.
MSH2
MSH2 (mutS homolog 2) is a human DNA mismatch repair gene on chromosome 2. Cloned in 1993, its pathogenic variants cause Lynch syndrome, Muir-Torre syndrome, and, biallelically, childhood cancer predisposition (CMMRD).
MSH3
MSH3 (mutS homolog 3, HGNC:7326), human gene at 5q14.1 encoding a DNA mismatch repair protein; with MSH2 forms MutSβ, recognizing insertion-deletion loops up to 13 nucleotides, linked to colorectal, bladder, and endometrial cancers.
MSH6
MSH6 (GTBP, HNPCC5) encodes the MutSα mismatch-recognition protein paired with MSH2; germline pathogenic variants cause Lynch syndrome type 5 with about 25% lifetime cancer risk, later colorectal cancer onset, and isolated MSH6 loss on tumor IHC.
PMS1
PMS1 (MLH2, hPMS1, HNPCC3) is a human protein-coding gene at 2q32.2 encoding a mutL/hexB-family mismatch repair protein that heterodimerizes with MLH1 (MutLβ). ClinGen refuted its asserted link to Lynch syndrome in 2023.
PMS2
PMS2 (PMS1 homolog 2) is a DNA mismatch repair gene on chromosome 7p22.1; its protein dimerizes with MLH1. Germline variants cause low-penetrance Lynch syndrome and, biallelically, CMMRD; the PMS2CL pseudogene complicates testing.