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Retinoic acid-induced protein 1 is a transcription factor that in humans is encoded by the RAI1 gene. Mutations or copy number alterations affecting this gene are associated with neurodevelopmental disorders. Deletions of RAI1 are a primary cause of Smith–Magenis syndrome, whereas duplications of the gene are associated with Potocki–Lupski syndrome.
The analysis highlights Standards and Overview as prominent areas in the source structure around RAI1.
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 RAI1 shows recurring relationship patterns in the source. For example, RAI1 → anterior amygdaloid area, Brodmann area 23, cardia, dorsomedial hypothalamic nucleus, habenula, human penis, lateral hypothalamus, lateral septal nucleus, mammillary body, nipple, olfactory tubercle, palpebral conjunctiva, parietal lobe, pylorus, retinal pigment epithelium, Rostral migratory stream, subiculum, tibia, urethra, ventromedial nucleus Another extracted example is RAI1 → circadian regulation of gene expression, cytoplasm, DNA-binding transcription factor activity, metal ion binding, mitochondrion, negative regulation of multicellular organism growth, nucleoplasm, nucleus, positive regulation of transcription by RNA polymerase II, positive regulation of transcription, DNA-templated, protein binding, regulation of transcription by RNA polymerase II, rhythmic process, skeletal system development. 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.
gene bp human chr band chromosome 17 retinoic protein location associated mouse transcription factor external syndrome 811 453 end 11
TTTA extracted 79 structured relationships around RAI1. Examples in this analysis include RAI1 → Aliases → RAI1, SMCR, SMS, retinoic acid induced 1 and RAI1 → Band → 17p11.2. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| RAI1 | Aliases | RAI1, SMCR, SMS, retinoic acid induced 1 | 1.00 | infobox |
| RAI1 | Band | 17p11.2 | 1.00 | infobox |
| RAI1 | Band | 11|11 B1.3-B2 | 1.00 | infobox |
| RAI1 | Bgee | retinal pigment epithelium | 1.00 | infobox |
| RAI1 | Bgee | nipple | 1.00 | infobox |
| RAI1 | Bgee | palpebral conjunctiva | 1.00 | infobox |
| RAI1 | Bgee | urethra | 1.00 | infobox |
| RAI1 | Bgee | pylorus | 1.00 | infobox |
| RAI1 | Bgee | tibia | 1.00 | infobox |
| RAI1 | Bgee | Brodmann area 23 | 1.00 | infobox |
| RAI1 | Bgee | cardia | 1.00 | infobox |
| RAI1 | Bgee | human penis | 1.00 | infobox |
| RAI1 | Bgee | parietal lobe | 1.00 | infobox |
| RAI1 | Bgee | lateral septal nucleus | 1.00 | infobox |
| RAI1 | Bgee | habenula | 1.00 | infobox |
| RAI1 | Bgee | anterior amygdaloid area | 1.00 | infobox |
| RAI1 | Bgee | olfactory tubercle | 1.00 | infobox |
| RAI1 | Bgee | ventromedial nucleus | 1.00 | infobox |
| RAI1 | Bgee | subiculum | 1.00 | infobox |
| RAI1 | Bgee | dorsomedial hypothalamic nucleus | 1.00 | infobox |
| RAI1 | Bgee | Rostral migratory stream | 1.00 | infobox |
| RAI1 | Bgee | lateral hypothalamus | 1.00 | infobox |
| RAI1 | Bgee | mammillary body | 1.00 | infobox |
| RAI1 | BioGPS | n/a | 1.00 | infobox |
| RAI1 | Chr. | Chromosome 17 (human) | 1.00 | infobox |
| RAI1 | Chr. | Chromosome 11 (mouse) | 1.00 | infobox |
| RAI1 | Databases | NCBI: entry; OMA: entry | 1.00 | infobox |
| RAI1 | End | 17,811,453 bp | 1.00 | infobox |
| RAI1 | End | 60,199,197 bp | 1.00 | infobox |
| RAI1 | Ensembl | ENSG00000108557 | 1.00 | infobox |
The concept neighborhoods around RAI1 bring nearby vocabulary together. In this analysis, examples include Retinoic, Gene and Acid. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
Bridges highlight paths between different parts of the RAI1 map and can reveal research angles that are easy to miss in a flat list.
TTTA analyzes the structure around RAI1 to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Standards & Overview, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — RAI1 · EN edition · Analysis: TopicsToTalkAbout