Pathway
Dravet syndrome
Dravet syndrome is a rare form of epilepsy. Between 70% and 80% of patients carry sodium channel α1 subunit gene (SCN1A) loss of function mutations. Truncating mutations (early stop codon) account...
WP:5200
What the reference databases state
Statements
29 statements
29 statements · 1 reference database · Subject: Dravet syndrome · Sources: WikiPathways
- AKT1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- CALM1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- CAMK2A participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- CHD2 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- FGF13 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- HCN1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- KCNA2 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- MAPK11 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- MAPKAP1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- MLST8 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- MTOR participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- NFKB1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
Show the remaining 17
- PCDH19 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- PIK3CA participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- PRKCA participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- PRR5 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- PRR5L participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- RICTOR participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN1A participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN1B participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN2A participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN2B participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN3A participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN3B participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN4B participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SCN8A participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- SNTA1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- STXBP1 participates in Dravet syndromeProteinWikiPathways WP5200Inferred only
- TNF participates in Dravet syndromeProteinWikiPathways WP5200Inferred only