Gene ontology · 67MSH2 → ADP binding, ATP binding, ATP-dependent activity, acting on DNA, ATPase activity, B cell differentiation, B cell mediated immunity, cellular response to DNA damage stimulus, centromeric DNA binding, chromatin binding, chromosome, damaged DNA binding, determination of adult lifespan, dinucleotide insertion or deletion binding, dinucleotide repeat insertion binding, DNA binding, DNA mismatch repair, DNA recombination, DNA repair, double-strand break repair, double-strand/single-strand DNA junction binding
Bgee · 19MSH2 → abdominal wall, Brodmann area 10, cerebellar hemisphere, epiblast, ganglionic eminence, gonad, middle frontal gyrus, otic placode, otic vesicle, primitive streak, rectum, retinal pigment epithelium, saccule, secondary oocyte, somite, tail of embryo, testicle, ventricular zone, zygote
RNA expression pattern · 19MSH2 → abdominal wall, Brodmann area 10, cerebellar hemisphere, epiblast, ganglionic eminence, gonad, middle frontal gyrus, otic placode, otic vesicle, primitive streak, rectum, retinal pigment epithelium, saccule, secondary oocyte, somite, tail of embryo, testicle, ventricular zone, zygote
related to Role in mismatch repair · 17MSH2 → ADP, ATP, ATPase, Conversely, DNA, In, MLH1, MSH3, MSH6, MutSα, MutSβ, N-terminal, NLS, Studies, The MSH2, The MutSα, When
related to Microsatellite instability · 13MSH2 → Because, Currently, Detection, DNA, HNPCC, If, IHC, MMR, MSI, PCR, PCR-based MSI, The, This
related to Epigenetic MSH2 deficiencies in cancer · 10MSH2 → ALL, DNA, Elevated DNA, If DNA, In, NSCLC, Reductions, See Frequencies, Such, There
related to Clinical significance · 9MSH2 → DNA, Hereditary, HNPCC, Lynch, MLH1, MSH2-MSH6, Mutations, MutSα, These
related to Interactions · 7MSH2 → ATR, BRCA1, CHEK2, EXO1, MAX, MSH3, MSH6
Band · 2MSH2 → 17 E4|17 57.87 cM, 2p21-p16.3
Chr. · 2MSH2 → Chromosome 17 (mouse), Chromosome 2 (human)
