Homo sapiens mutS homolog 2 (MSH2), transcript variant 15, mRNA

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Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies. [Mol Cell. 2024]
Multisite phosphorylation dictates selective E2-E3 pairing as revealed by Ubc8/UBE2H-GID/CTLH assemblies.
Chrustowicz J, Sherpa D, Li J, Langlois CR, Papadopoulou EC, Vu DT, Hehl LA, Karayel Ö, Beier V, von Gronau S, et al. Mol Cell. 2024 Jan 18; 84(2):293-308.e14. Epub 2023 Dec 18.
Rare single-nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndrome. [Cancer Rep (Hoboken). 2024]
Rare single-nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndrome.
Mirabdolhosseini SM, Yaghoob Taleghani M, Rejali L, Sadeghi H, Fatemi N, Tavallaei M, Famil Meyari A, Saeidi N, Ketabi Moghadam P, Sadeghi A, et al. Cancer Rep (Hoboken). 2024 Jan; 7(1):e1930. Epub 2023 Nov 2.
Novel MSH2 and TSC2 variants in a Chinese family with Lynch syndrome and their synergistic impact in urothelial carcinoma. [Transl Res. 2024]
Novel MSH2 and TSC2 variants in a Chinese family with Lynch syndrome and their synergistic impact in urothelial carcinoma.
Li M, Yan X, Liu H, Miao W, Wu W, Zhao Y, Wang C, Liu H. Transl Res. 2024 Mar; 265:26-35. Epub 2023 Oct 31.

RefSeq protein product
See the reference protein sequence for DNA mismatch repair protein Msh2 isoform 13 (NP_001393572.1).

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Nucleotide