Research any topic before you write.
Find related topics. | Discover entities. | See connections. | Build a topical map.
ARHGAP11B is a human-specific gene that amplifies basal progenitors, controls neural progenitor proliferation, and contributes to neocortex folding. It is capable of causing neocortex folding in mice. This likely reflects a role for ARHGAP11B in development and evolutionary expansion of the human neocortex, a conclusion consistent with the finding that…
The analysis highlights Function, Human evolution and Structure as prominent areas in the source structure around ARHGAP11B.
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 ARHGAP11B shows recurring relationship patterns in the source. For example, ARHGAP11B → appendix, bone marrow, bone marrow cell, ganglionic eminence, gonad, lymph node, monocyte, stromal cell of endometrium, testicle, ventricular zone Another extracted example is ARHGAP11B → ARHGAP11A, ARHGAP11A1-220, C-terminal, In, RhoA/Rho-kinase, RhoGAP, This. 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.
neocortex human gene activity bp arhgap11a rhogap folding development chr chromosome 15 function likely expansion evolution band rho nucleotide evolutionary
TTTA extracted 64 structured relationships around ARHGAP11B. Examples in this analysis include ARHGAP11B → Aliases → ARHGAP11B, B'-T, FAM7B1, Rho GTPase activating protein 11B, GAP (1-8), ArhGAP11B and human encephalisation and ARHGAP11B → Band → 15q13.2. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| ARHGAP11B | Aliases | ARHGAP11B, B'-T, FAM7B1, Rho GTPase activating protein 11B, GAP (1-8), ArhGAP11B and human encephalisation | 1.00 | infobox |
| ARHGAP11B | Band | 15q13.2 | 1.00 | infobox |
| ARHGAP11B | Bgee | testicle | 1.00 | infobox |
| ARHGAP11B | Bgee | bone marrow | 1.00 | infobox |
| ARHGAP11B | Bgee | bone marrow cell | 1.00 | infobox |
| ARHGAP11B | Bgee | ganglionic eminence | 1.00 | infobox |
| ARHGAP11B | Bgee | stromal cell of endometrium | 1.00 | infobox |
| ARHGAP11B | Bgee | ventricular zone | 1.00 | infobox |
| ARHGAP11B | Bgee | gonad | 1.00 | infobox |
| ARHGAP11B | Bgee | lymph node | 1.00 | infobox |
| ARHGAP11B | Bgee | monocyte | 1.00 | infobox |
| ARHGAP11B | Bgee | appendix | 1.00 | infobox |
| ARHGAP11B | BioGPS | n/a | 1.00 | infobox |
| ARHGAP11B | Chr. | Chromosome 15 (human) | 1.00 | infobox |
| ARHGAP11B | Databases | NCBI: entry; OMA: entry | 1.00 | infobox |
| ARHGAP11B | End | 30,649,529 bp | 1.00 | infobox |
| ARHGAP11B | Ensembl | ENSG00000274734 ENSG00000286139 ENSG00000285077 | 1.00 | infobox |
| ARHGAP11B | Entrez | 89839 | 1.00 | infobox |
| ARHGAP11B | External IDs | OMIM: 616310; GeneCards: ARHGAP11B | 1.00 | infobox |
| ARHGAP11B | Gene location (Human) | Gene location (Human)Chr.Chromosome 15 (human)Band15q13.2Start30,624,494 bpEnd30,649,529 bp | 1.00 | infobox |
| ARHGAP11B | Gene ontology | GTPase activator activity | 1.00 | infobox |
| ARHGAP11B | Gene ontology | cytosol | 1.00 | infobox |
| ARHGAP11B | Gene ontology | regulation of small GTPase mediated signal transduction | 1.00 | infobox |
| ARHGAP11B | Gene ontology | signal transduction | 1.00 | infobox |
| ARHGAP11B | Gene ontology | cerebral cortex development | 1.00 | infobox |
| ARHGAP11B | Gene ontology | positive regulation of GTPase activity | 1.00 | infobox |
| ARHGAP11B | Location (UCSC) | Chr 15: 30.62 – 30.65 Mb | 1.00 | infobox |
| ARHGAP11B | Orthologs | OrthologsDatabasesNCBI: entry; OMA: entrySpeciesHumanMouseEntrez89839n/aEnsemblENSG00000274734 ENSG00000286139 ENSG00000285077n/aUniProtQ3KRB8n/aRefSeq (mRNA)NM_001039841n/aRefS… | 1.00 | infobox |
| ARHGAP11B | RefSeq (mRNA) | NM_001039841 | 1.00 | infobox |
| ARHGAP11B | RefSeq (protein) | NP_001034930 | 1.00 | infobox |
The concept neighborhoods around ARHGAP11B bring nearby vocabulary together. In this analysis, examples include Neocortex, Gene and Human. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For ARHGAP11B, one of the stronger structural bridges in this analysis connects ARHGAP11B with Function. 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 ARHGAP11B to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Function, Human evolution & Structure, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — ARHGAP11B · EN edition · Analysis: TopicsToTalkAbout