Source of data/description of the gene set | Short name of the data source and the gene set | Number of genes | Number of publications or database query |
---|---|---|---|
Research papers and review articles on FB-regulating genes | Publications (Additional file 1: Table S1) | 105 | 17 review articles, 45 research papers |
OMIM/genes possessing allelic variants associated with obesity, hyperphagia, or anorexia | OMIM_allelic_variants (Additional file 1: Table S2) | 73 | Command used in OMIM search: ‘hyperphagia’ OR ‘obesity’ OR ‘anorexia’ (Records with: gene map locus; Prefixes: +, *; Search in: allelic variants) |
OMIM/terms obesity, or hyperphagia, or anorexia were found in text fields (excluding the chapter devoted to allelic variants). | OMIM_all_text a (Additional file 1: Table S2) | 263 | Command used in OMIM search: ‘hyperphagia’ OR ‘obesity’ OR ‘anorexia’ (Records with: gene map locus; Prefixes: +, *; Search in: all text) * |
OMIM and research papers/Genes whose mutant variants are implicated in the Bardet-Biedl and other syndromes associated with obesity. | Syndromes (Additional file 1: Table S3) | 37 | OMIM entries: 1) #209900; BARDET-BIEDL SYNDROME 1 (Genetic Heterogeneity of Bardet-Biedl Syndrome) 2) #176270; PRADER-WILLI SYNDROME 3) #203800; ALSTROM SYNDROME 4) #216550; COHEN SYNDROME 5) #103580; PSEUDOHYPOPARA-THYROIDISM, TYPE IA 6) #201000; CARPENTER SYNDROME 1 7) #147920; KABUKI SYNDROME 1; 8) #300867; KABUKI SYNDROME 2; 9) #157980; MOMO SYNDROME 10) #301900; BORJESON-FORSSMAN-LEHMANN SYNDROME 11) #182290; SMITH-MAGENIS SYNDROME 12) #180849; RUBINSTEIN-TAYBI SYNDROME 1 13) #612469; WAGRO SYNDROME; 3 review articles, 1 research paper |
GWAS meta-analysis papers/genes located in the vicinity of a lead SNP | GWAS meta-analysis (Additional file 1: Table S4) | 184 | 9 research articles |