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MSH2

MSH2 MSH2 is a DNA mismatch repair gene discussed here in relation to Lynch syndrome.

MSH2 is a DNA mismatch repair gene discussed here in relation to Lynch syndrome. In this study, disease-related inherited variants in MSH2 were found in some people and families with colorectal and other Lynch syndrome-associated cancers, including one pathogenic variant shared across a large related group.

Sources

Drafting source: Wanitsuwan Worrawit; Kanjanapradit Kanet; Jearanai Supakool; Suphasynth Yuthasak; Supaattagorn Pongsatorn; Vijasika Sukanya; Wanram Surasak; Ngamphiw Chumpol; Nakhonsri Vorthunju; Tongsima Sissades; Satsue Palakorn; Sangkeaw Natnaree; Horpaopan Sukanya. WGS identifies Lynch syndrome (LS) patients and uncovers a large family with MSH2 -related LS in Southern Thailand. 2026; DOI 10.1371/journal.pone.0348867; article XML SHA-256 ec1fa8b9bf91ecdd9a0c3442b7af166347c616106acc448850e4c2cda8ed5051. “WGS identifies Lynch syndrome (LS) patients and uncovers a large family with MSH2 -related LS in Southern Thailand” (10.1371/journal.pone.0348867).
CC-BY-4.0 · Definition uses new wording; original source retains its stated licence. · Source snapshot SHA-256: ec1fa8b9bf91ecdd9a0c3442b7af166347c616106acc448850e4c2cda8ed5051

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Cite this entry

PsychTerms (psychterms.org), CC BY 4.0, version 1. “MSH2.” Development preview.

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