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Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and anion channel in vertebrates that is encoded by the CFTR gene.
The analysis highlights Geography, Gene and Tissue and intracellular localization as prominent areas in the source structure around Cystic fibrosis transmembrane conductance regulator.
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 Cystic fibrosis transmembrane conductance regulator shows recurring relationship patterns in the source. For example, Cystic fibrosis transmembrane conductance regulator → apical plasma membrane, ATP binding, ATPase activity, ATPase-coupled inorganic anion transmembrane transporter activity, ATPase-coupled transmembrane transporter activity, bicarbonate transmembrane transporter activity, bicarbonate transport, cell surface, cellular response to cAMP, cellular response to forskolin, chaperone binding, chloride channel activity, chloride channel complex, chloride channel inhibitor activity, chloride channel regulator activity, chloride transmembrane transport, chloride transmembrane transporter activity, chloride transport, cholesterol biosynthetic process, cholesterol transport Another extracted example is Cystic fibrosis transmembrane conductance regulator → body of pancreas, C1 segment, crypt of lieberkuhn of small intestine, duodenum, epithelium of small intestine, gallbladder, Ileal epithelium, islet of Langerhans, jejunal mucosa, jejunum, left colon, left lung lobe, migratory enteric neural crest cell, minor salivary glands, mucosa of sigmoid colon, mucosa of transverse colon, Paneth cell, rectum, spermatid. 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.
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TTTA extracted 155 structured relationships around Cystic fibrosis transmembrane conductance regulator. Examples in this analysis include Cystic fibrosis transmembrane conductance regulator → 5.6.1.6 → ↗ and Cystic fibrosis transmembrane conductance regulator → Aliases → CFTR, ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-dJ760C5.1, cystic fibrosis transmembrane conductance regulator, CF transmembrane conductance regulator. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Cystic fibrosis transmembrane conductance regulator | 5.6.1.6 | ↗ | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Aliases | CFTR, ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-dJ760C5.1, cystic fibrosis transmembrane conductance regulator, CF transmembrane conductance regulator | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Available structures | Available structuresPDBOrtholog search: PDBe RCSB List of PDB id codes1XMI, 1XMJ, 2BBO, 2BBS, 2BBT, 2LOB, 2PZE, 2PZF, 2PZG, 3GD7, 3ISW, 4WZ6, 5D2D, 5D3E, 5D3F | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Band | 7q31.2 | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Band | 6 A2|6 8.1 cM | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | body of pancreas | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | gallbladder | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | rectum | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | mucosa of sigmoid colon | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | islet of Langerhans | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | duodenum | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | mucosa of transverse colon | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | jejunal mucosa | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | C1 segment | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | minor salivary glands | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | Paneth cell | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | epithelium of small intestine | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | Ileal epithelium | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | left colon | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | crypt of lieberkuhn of small intestine | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | jejunum | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | left lung lobe | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | migratory enteric neural crest cell | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Bgee | spermatid | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | BioGPS | n/a | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Chr. | Chromosome 7 (human) | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Chr. | Chromosome 6 (mouse) | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | Databases | NCBI: entry; OMA: entry | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | End | 117,715,971 bp | 1.00 | infobox |
| Cystic fibrosis transmembrane conductance regulator | End | 18,322,767 bp | 1.00 | infobox |
The concept neighborhoods around Cystic fibrosis transmembrane conductance regulator bring nearby vocabulary together. In this analysis, examples include Fibrosis, Mutations and Conductance. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Cystic fibrosis transmembrane conductance regulator, one of the stronger structural bridges in this analysis connects Cystic fibrosis transmembrane conductance regulator 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 Cystic fibrosis transmembrane conductance regulator to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Geography, Gene & Tissue and intracellular localization, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Cystic fibrosis transmembrane conductance regulator · EN edition · Analysis: TopicsToTalkAbout