Figure 4From: A survey of protein interaction data and multigenic inherited disordersLiddle syndrome. Mutations in either SCNNB or SCNNG are associated with Liddle syndrome (disease group 772). Both are subunits of the heterotrimeric (alpha, beta, gamma) nonvoltage-gated, amiloride-sensitive, sodium channel. Both proteins were observed together with SCNN1A (the alpha subunit of the channel) as interactors with syntaxin 1A (STX1A). The original paper[32] contains evidence for a direct interaction between STX1A and the gamma subunit and for a complex that includes all four proteins using in-vitro translated components (Figure one in[32]). The complex is represented as four binary interactions in the BioGrid database. These interactions are identified as part of a potential spoke-represented complex by iRefScape (a grey hexagon appears after selecting View Tools/Show spoke-represented complexes from the iRefScape menu).Back to article page