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. 2013 May 2;92(5):667–680. doi: 10.1016/j.ajhg.2013.03.022

Table 1.

Top Predicted Genes for Crohn Disease

Gene LBF p Value GWAS Hit Supporting Evidence p Value (Rep.)
UBE2L3 7.78 2.2 × 10−6 no associated with celiac disease, rheumatoid arthritis, and lupus34 4.2 × 10−6
ORMDL3 5.72 3.3 × 10−5 yes associated with Crohn disease and ulcerative colitis29,33 1.0 × 10−6
PTGER4 5.57 3.7 × 10−5 yes associated with Crohn disease33 3.4 × 10−5
IK 5.43 4.3 × 10−5 no regulates class II MHC antigen, which is associated with autoimmune diseases38 0.75
LYNX1 5.34 4.8 × 10−5 no agonist of nonneuronal nAchR pathway, which may be important for IBD39–41 0.014
NUDT4 5.32 4.8 × 10−5 no NA 3.4 × 10−5
EFS 5.23 6.1 × 10−5 no knockout mice exhibit symptoms similar to Crohn disease36,37 0.039
FAM96A 5.19 6.3 × 10−5 no NA 4.2 × 10−6
SLC22A5 5.17 6.3 × 10−5 yes associated with Crohn disease29,33 3.8 × 10−5
ANAPC2 4.87 9.2 × 10−5 no NA 0.0006

The LBF column is the logarithm of the Bayes Factor for the genes. The p values refer to the p values of LBFs, calculated from simulations. The “GWAS hit” column shows whether a gene has been implicated as a candidate gene in previous GWASs. The last column shows the p value of the genes using an independent GWAS data set of Crohn disease (replication). See the text for details of the supporting evidence.