Sodium Channels Topologies
Basic Principles
Instructions:
- Mouse over a residue – a table for the corresponding protein position will show at the bottom of the page
- Enter the numeric protein position in the box provided above; the format is flexible as long as the entered variant contains the numeric position
- To freeze the table, either click on the protein position entry field or simply press Enter
- Use mouse scrolling to view the table at the bottom of the page
- Repeated action will unfreeze the table
- Once a particular position is chosen, the vector graphics can be printed or exported in PDF format
Topology of the Table
Additional Details:
- The best way to print the topology of the gene and the table below is by pressing Ctrl+P
- It might be necessary to scale down the image size before printing by adjusting the scale factor in your printer menu (advanced printer settings)
- The framework is displayed best in Chrome browser. Using Internet Explorer or other browsers might present issues with printing, displaying a specific mutation, etc.
- Unless specifically stated differently in the mutation description table, the following reference isoforms are used:
- SCN1A – NM_001165963
- SCN2A – NM_001040142
- SCN8A – NM_014191
- All the genomic positions are in HG19 coordinates
- Only missense mutations are displayed on the topologies.
References
- All the mutations displayed in the database are missense mutations. The following sources have been used for SCN1A, SCN2A and SCN8A mutations:
- Meng H, Xu HQ, Yu L, Lin GW, He N, Su T, et al (2015) The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype. Hum Mutation 36(6): 573-580
- Wolff M, Johannesen KM, Hedrich UB, Masnada S, Rubboli G, Gardella E, et al (2017) Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders. Brain 140(5): 1316–1336.
- SCN8A.net