BBS2 and hereditary disease: Genetic interactions such as aldolase B (ALDOB) with the Bardet-Biedl syndrome proteins 1, 2, 4, 7 (BBS1, BBS2, BBS4, BBS7) and thus a connection between the glycolysis and the ciliopathic human genetic disorder of the Bardet-Biedl syndrome are easily detected via the interaction view relation search (VRelation) of GoSynthetic (steps: see tutorial in Supplementary Material).