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. 2012 Jun 22;7(6):e37708. doi: 10.1371/journal.pone.0037708

Table 4. Differentially-expressed genes that distinguish severe IPF from control.

Gene Symbol Description Fold Change
IL1R2 interleukin 1 receptor, type II 3.43
DEFA3 defensing, alpha 3, neutrophil specific 3.39
OLFM4 olfactomedin 4 3.39
MMP9 matrix metallopeptidase 9 (gelatinase B) 3.32
GRB10 growth factor receptor-bound protein 10 3.25
DEFA4 defensin, alpha 4, corticostatin 3.00
LTF lactotransferrin 2.97
RAB8A RAB8A, member RAS oncogene family 2.76
CTSG cathepsin G 2.64
CAMP cathelicidin antimicrobial peptide 2.64
CEACAMP8 carcinoembryonic antigen-related cell adhesion (8) 2.53
VSIG4 V-set and immunoglobulin domain containing 4 2.50
PGLYRP1 peptidoglycan recognition protein 1 2.45
FKBP5 FK506 binding protein 5 2.45
LOC151438 hypothetical protein LOC151438 2.43
ECHDC3 enoyl Coenzyme A hydratase domain containing 3 2.34
LOC100130890 similar to hCG2030844 −2.34
PRSS36 protease, serine, 36 −2.37
MCAT malonyl CoA:ACP acyltransferase (mitochondrial) −2.42
IGHM immunoglobulin heavy constant mu −3.0

Significance analysis of microarrays (SAM) of IPF samples when categorized by percent predicted DLCO ≤35% [N = 15]. Differentially- expressed transcripts with <1% false discovery rate and ≥ 2-fold change in expression are represented. Fold changes are expressed as log2 ratio. See supplementary tables for a complete list of differentially-expressed genes and corresponding accession numbers.