| Gene Symbol | ent-gene-62420ab9 |
| Causality strength | Strong - DCTN1 mutations cause Perry syndrome with high penetrance |
| Population frequency | Very rare (<0.0001% of population) |
| Age of onset | Typically 45-65 years |
| Segregation | Autosomal dominant inheritance demonstrated in multiple families |
| Unique feature | DCTN1 mutations cause both atypical parkinsonism (Perry) and ALS phenotypes |
| KG Connections | 2 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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