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DNA mismatch repair protein Msh2 also known as MutS homolog 2 or MSH2 is a protein that in humans is encoded by the MSH2 gene, which is located on chromosome 2. MSH2 is a tumor suppressor gene and more specifically a caretaker gene that codes for a DNA mismatch repair (MMR) protein, MSH2, which forms a heterodimer with MSH6 to make the human MutSα…
The analysis highlights Epigenetic MSH2 deficiencies in cancer, Interactions and Clinical significance as prominent areas in the source structure around MSH2.
Source areas are shown by the number of related topics found in each part of the analysis. Use smaller areas too: they can reveal specialized angles and content gaps.
Smaller areas are not necessarily less important. They contain fewer connections in this analysis and can be useful for finding specialized angles or coverage gaps.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the complete topic structure, not only the most central items. Less prominent entities and concepts can reveal missing angles, specialized context and useful research gaps. Each item opens a new analysis centered on that subject.
Deeper signals for content research, entity SEO and topical coverage. The plain-language headings explain what each technical view is useful for.
The extracted context around MSH2 shows recurring relationship patterns in the source. For example, MSH2 → 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 Another extracted example is MSH2 → 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. Use these groups to spot repeated connection types before inspecting the individual relationships.
Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
dna repair mutations gene mismatch msh6 protein mutsα cancer human complex chromosome microsatellite bp instability damage genes msh3 chr band
TTTA extracted 188 structured relationships around MSH2. Examples in this analysis include MSH2 → Aliases → MSH2, mutS homolog 2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2, hMMRCS2, MSH-2 and MSH2 → Available structures → Available structuresPDBOrtholog search: PDBe RCSB List of PDB id codes2O8B, 2O8C, 2O8D, 2O8E, 2O8F, 3THW, 3THX, 3THY, 3THZ. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| MSH2 | Aliases | MSH2, mutS homolog 2, COCA1, FCC1, HNPCC, HNPCC1, LCFS2, hMMRCS2, MSH-2 | 1.00 | infobox |
| MSH2 | Available structures | Available structuresPDBOrtholog search: PDBe RCSB List of PDB id codes2O8B, 2O8C, 2O8D, 2O8E, 2O8F, 3THW, 3THX, 3THY, 3THZ | 1.00 | infobox |
| MSH2 | Band | 2p21-p16.3 | 1.00 | infobox |
| MSH2 | Band | 17 E4|17 57.87 cM | 1.00 | infobox |
| MSH2 | Bgee | secondary oocyte | 1.00 | infobox |
| MSH2 | Bgee | ventricular zone | 1.00 | infobox |
| MSH2 | Bgee | ganglionic eminence | 1.00 | infobox |
| MSH2 | Bgee | gonad | 1.00 | infobox |
| MSH2 | Bgee | retinal pigment epithelium | 1.00 | infobox |
| MSH2 | Bgee | testicle | 1.00 | infobox |
| MSH2 | Bgee | middle frontal gyrus | 1.00 | infobox |
| MSH2 | Bgee | Brodmann area 10 | 1.00 | infobox |
| MSH2 | Bgee | rectum | 1.00 | infobox |
| MSH2 | Bgee | cerebellar hemisphere | 1.00 | infobox |
| MSH2 | Bgee | primitive streak | 1.00 | infobox |
| MSH2 | Bgee | saccule | 1.00 | infobox |
| MSH2 | Bgee | epiblast | 1.00 | infobox |
| MSH2 | Bgee | otic placode | 1.00 | infobox |
| MSH2 | Bgee | otic vesicle | 1.00 | infobox |
| MSH2 | Bgee | tail of embryo | 1.00 | infobox |
| MSH2 | Bgee | somite | 1.00 | infobox |
| MSH2 | Bgee | zygote | 1.00 | infobox |
| MSH2 | Bgee | abdominal wall | 1.00 | infobox |
| MSH2 | BioGPS | More reference expression data | 1.00 | infobox |
| MSH2 | Chr. | Chromosome 2 (human) | 1.00 | infobox |
| MSH2 | Chr. | Chromosome 17 (mouse) | 1.00 | infobox |
| MSH2 | Databases | NCBI: entry; OMA: entry | 1.00 | infobox |
| MSH2 | End | 47,663,146 bp | 1.00 | infobox |
| MSH2 | End | 88,031,141 bp | 1.00 | infobox |
| MSH2 | Ensembl | ENSG00000095002 | 1.00 | infobox |
The concept neighborhoods around MSH2 bring nearby vocabulary together. In this analysis, examples include Msh6, Repair and Protein. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For MSH2, one of the stronger structural bridges in this analysis connects MSH2 with Overview. Bridges highlight paths between different parts of the map and can reveal research angles that are easy to miss in a flat list.
TTTA analyzes the structure around MSH2 to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Epigenetic MSH2 deficiencies in cancer, Interactions & Clinical significance, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — MSH2 · EN edition · Analysis: TopicsToTalkAbout