Rotatin (RTTN)
Homo sapiens — UniProt Q86VV8
Data last refreshed: (UniProt release unknown)
Key facts
Rotatin (RTTN) is a protein from Homo sapiens identified by UniProt accession Q86VV8, 2226 residues long. MolForge cross-references it against 0 known binders and 53 disease associations.
- UniProt accession: Q86VV8; gene symbol RTTN.
- Organism: Homo sapiens.
- Length: 2226 amino acids.
- Top disease associations (Open Targets): microcephalic primordial dwarfism due to RTTN deficiency, bilateral generalized polymicrogyria and bilateral polymicrogyria.
- 3D structure: AlphaFold model available.
Target properties
| Protein name | Rotatin |
|---|---|
| UniProt accession | Q86VV8 |
| Gene | RTTN |
| Organism | Homo sapiens |
| Length | 2226 residues |
| Molecular weight | — |
| EC numbers | — |
| Target class | — |
| Subcellular location | — |
| Keywords | — |
Druggability
Target tractability assessment (Open Targets + pocket analysis). No approved drug
| Druggability tier | MEDIUM |
|---|---|
| Druggability score | — |
| Pocket score | — |
| Max clinical phase | — |
Disease associations (53)
Diseases linked to this target (Open Targets).
- microcephalic primordial dwarfism due to RTTN deficiency · score 0.76
- bilateral generalized polymicrogyria · score 0.68
- bilateral polymicrogyria · score 0.54
- mean corpuscular volume · score 0.49
- Primary microcephaly · score 0.47
- Microcephaly · score 0.41
- mean reticulocyte volume · score 0.41
- mean platelet volume · score 0.41
- Intellectual disability · score 0.37
- autosomal recessive primary microcephaly · score 0.37
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
|---|---|---|---|---|
| AF-Q86VV8-F1 | alphafold | PREDICTED | 77.14 | — |
Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q86VV8.
Amino-acid sequence (2226 residues)
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
Which diseases are associated with RTTN?
The strongest Open Targets associations for RTTN are microcephalic primordial dwarfism due to RTTN deficiency, bilateral generalized polymicrogyria, bilateral polymicrogyria, mean corpuscular volume and Primary microcephaly.
How long is the RTTN protein?
The Homo sapiens RTTN protein (UniProt Q86VV8) is 2226 amino acids long.
Browse: Targets: R · all protein targets A–Z · drugs A–Z.
Sources
- UniProtKB Q86VV8 — name, gene, function, sequence, keywords (CC BY 4.0)
- AlphaFold DB Q86VV8 — predicted 3D structure (CC BY 4.0)
- Open Targets Platform — disease associations and tractability (CC0)
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