Mouse Gene Set: WP_DRAVET_SYNDROME_SCN1AA1783V_POINT_MUTATION_MODEL


Standard name WP_DRAVET_SYNDROME_SCN1AA1783V_POINT_MUTATION_MODEL
Systematic name MM16641
Brief description Dravet syndrome: Scn1a-A1783V point mutation model
Full description or abstract  
Collection M2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP5298
Related gene sets  
External links https://www.wikipathways.org/pathways/WP5298
Filtered by similarity ?
Source species Mus musculus
Contributed by WikiPathways
Source platform or
identifier namespace		 Mouse_NCBI_Gene_ID
Dataset references  
Download gene set format: grp | gmt | xml | json | TSV metadata
Compute overlaps ? (show collections to investigate for overlap with this gene set)
Compendia expression profiles ? NG-CHM interactive heatmaps
(Please note that clustering takes a few seconds)
Mouse Transcriptomic BodyMap compendium

Legacy heatmaps (PNG)
Mouse Transcriptomic BodyMap compendium
Advanced query Further investigate these 72 genes
Show members (show 72 source identifiers mapped to 72 genes)
Version history 2024.1.Mm: Renamed from WP_DRAVET_SYNDROME_SCN1A_A1783V_POINT_MUTATION_MODEL. Updated to WikiPathways Release 20240710

See MSigDB license terms here. Please note that certain gene sets have special access terms.