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. 2016 Nov 4;17:874. doi: 10.1186/s12864-016-3198-9

Table 3.

Pathways associated with fasting glucose across human and mouse association datasets

Pathway MSEA Meta-MSEA
Human Mouse Mouse Mouse
GWAS GWAS TWAS EWAS Value FDR
Glycolysis/Gluconeogenesis 2.56 0.88 3.84 0.63 4.73 2.22 %
Starch and sucrose metabolism 3.67 1.37 3.29 0.17 4.57 2.22 %
Regulation And Function Of ChREBP in Liver 3.10 0.93 2.74 0.41 4.08 3.60 %
Nuclear Receptors in Lipid Metabolism and Toxicity 5.58 0.48 1.99 0.35 4.00 3.60 %
Regulation of gene expression in beta cells 4.16 1.75 1.48 0.19 3.97 3.60 %
Type II diabetes mellitus 2.11 1.09 1.48 1.08 3.66 6.00 %
Integration of energy metabolism 2.42 0.33 2.17 1.09 3.34 10.82 %
Steroid biosynthesis 1.10 2.04 1.27 0.76 3.10 14.34 %
alpha-linolenic acid (ALA) metabolism 3.40 0.32 1.72 0.69 3.09 14.34 %
Incretin Synthesis, Secretion and Inactivation 3.24 1.14 0.09 2.06 3.02 14.34 %
Adipocytokine signaling pathway 2.55 0.41 1.13 1.26 2.94 14.34 %
Chylomicron-mediated lipid transport 0.43 0.89 2.89 1.26 2.92 14.34 %
Glucose transport 5.57 1.31 0.27 0.29 2.92 14.34 %

The results are listed as − log10 P-values, and the full table is available in Additional file 5. MSEA was run with top 50 % of markers, and an LD cutoff r2 < 50 % was applied to the GWAS. For the human GWAS, SNPs were assigned to genes based on a 20 kb window in the genome sequence. For the mouse GWAS, liver eQTL data were used for gene assignment. The Bonferroni-adjusted 5 % significance level for 1346 independent tests is at − log10P = 4.43