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. 2016 Mar 8;18(4):370–385. doi: 10.1177/1099800416629209

Table 2.

Differentially Expressed Genes.

Probe Symbol Name Fold Changea ENTREZ Gene ID Directionb p adjusted c Primary Roled
Limma
 ILMN_1684308 DEFB103B Defensin, β 103B (DEFB103B) 0.10 55894 Down .0489 I
Gene pattern
 ILMN_1873793 Hs.650028 cDNA FLJ25030 fis, clone CBL02631 0.18 Up < .0001 U
 ILMN_1655418 CAPNS1 Calpain, small subunit 1 0.58 826 Down < .0001 I
 ILMN_1705605 MGC13005 PREDICTED: Homo sapiens hypothetical protein MGC13005 0.83 Down < .0001 U
 ILMN_1728799 FBP1 Fructose-1,6-bisphosphatase 1 0.75 2203 Down < .0001 M
 ILMN_1808821 COMMD9 COMM domain containing 9 Transcription elongation factor A (SII)-like 1, transcript variant 0.59 29099 Down < .0001 I
 ILMN_2398408 TCEAL1 2 0.18 9338 Down < .0001 I/M
 ILMN_1653115 ECH1 Enoyl Coenzyme A hydratase 1, peroxisomal 0.46 1891 Down < .0001 M
 ILMN_1759652 C1orf61 chromosome 1 open reading frame 61 0.16 10485 Down < .0001 U
 ILMN_1666269 CTSZ Cathepsin Z Yip1 interacting factor homolog B (S. cerevisiae), transcript 0.77 1522 Down < .0001 I
 ILMN_2363668 YIF1B variant 4 0.55 90522 Down < .0001 I/M/S
 ILMN_1791211 DOK2 Docking protein 2, 56kDa 0.75 9046 Down < .0001 I

Note. aFold change of the log2-transformed, background-corrected, quantile-normalized intensity gene expression values in the high- as compared to low-evening-fatigue group. bDirection of difference in gene expression in the high- as compared to the low-evening-fatigue group. cPadjusted = Benjamini-Hochberg adjusted p value. dThe primary functional role(s) of a given gene is identified as follows: M = metabolism, protein synthesis (n = 4); I = immune activation and immune cell replenishment (n = 7); S = serotonergic activation (n = 1); and U = unknown (n = 3).