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. 2016 Nov 11;12(11):e1005195. doi: 10.1371/journal.pcbi.1005195

Table 3. Shared molecular bases of T2D, BD, and CAD as revealed by NetPocos.

Gene Name Frequency T2D BD CAD
CAD
WWOX 102 NO YES YES
CSMD1 80 NO YES NO
APP 77 NO NO NO
PARK2 74 YES YES NO
GRID1 64 YES YES NO
DOCK10 61 YES NO NO
CUL3 56 NO NO NO
DENND1A 56 NO NO NO
CD36 52 NO YES YES
CNTNAP2 49 NO YES NO
T2D
CSMD1 38 NO YES NO
A2BP1 35 NO YES NO
FHIT 35 NO NO NO
CNTNAP2 34 NO YES NO
PTPRD 32 YES YES NO
CACNA2D3 31 NO NO NO
WWOX 29 NO YES YES
NRG1 28 YES YES YES
SUPT3H 28 YES NO NO
CDH13 26 NO YES YES
BD
PARK2 54 YES YES NO
NRG1 48 YES YES YES
ADRB2 47 YES YES YES
WWOX 43 NO YES YES
APP 41 NO NO NO
CACNA2D3 40 NO NO NO
CUL3 40 NO NO NO
KIF16B 40 NO NO NO
SNX29 35 NO NO NO
DAPK1 33 NO NO NO

For each disease, ten most frequent genes that are involved in NetPocos selected by L1 regularized logistic regression in risk prediction are listed. Previously reported association of these genes with the three diseases are indicated with a “Yes” or “No” in the respective column of each row.