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. Author manuscript; available in PMC: 2016 Sep 13.
Published in final edited form as: JAMA Ophthalmol. 2015 Jul;133(7):770–777. doi: 10.1001/jamaophthalmol.2015.0726

Table 2.

Probe Sets With Some of the Highest Signals in Orbital Adipose Tissue Compared With Uninflamed Controlsa

Probe Set Gene Title Fold Difference P Value for FDR
209396_s_at Chitinase 3–like 1 (cartilage glycoprotein-39) 93.5 1.5 × 10−6
1555745_a_at Lysozyme 93.3 8.98 × 10−7
214677_x_at Immunoglobulin λ constant 1 (Mcg marker) 53.5 1.84 × 10−4
224795_x_at Immunoglobulin κ locus; immunoglobulin kappa constant 45.0 2.00 × 10−4
217022_s_at Immunoglobulin heavy locus; immunoglobulin heavy constant α 1; immunoglobulin heavy constant α 2 (A2m marker) 42.8 1.22 × 10−4
203915_at Chemokine (C-X-C motif) ligand 9 35.0 6.22 × 10−5
215121_x_at Immunoglobulin λ light chain-like; immunoglobulin λ constant 1 (Mcg marker); immunoglobulin λ variable 1–44 34.8 3.47 × 10−4
216491_x_at Immunoglobulin heavy constant μ 34.2 7.80 × 10−5
212671_s_at Major histocompatibility complex, class II, DQ α 1, DQ α 2, DQ α 1 chain–like 30.9 1.05 × 10−5
209875_s_at Secreted phosphoprotein 1 29.5 2.39 × 10−3
1555756_a_at C-type lectin domain family 7, member A 28.9 7.07 × 10−5
202834_at Angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 28.3 9.29 × 10−5
219386_s_at SLAM family member 8 25.5 7.40 × 10−6
219159_s_at SLAM family member 7 24.7 1.16 × 10−4
222838_at SLAM family member 7 23.3 2.12 × 10−5
211429_s_at Serpin peptidase inhibitor, clade A (α-1 antiproteinase, antitrypsin), member 1 21.1 4.50 × 10−5
209696_at Fructose-1,6-bisphosphatase 1 18.4 1.63 × 10−7
205890_s_at GABA B receptor, 1; ubiquitin D 18.3 7.05 × 10−5
203936_s_at Matrix metallopeptidase 9 (gelatinase B, 92-kDa gelatinase, 92-kDa type IV collagenase) 17.7 1.17 × 10−6
209201_x_at Chemokine (C-X-C motif) receptor 4 17.4 3.32 × 10−5

Abbreviations: FDR, false discovery rate; GABA, γ-aminobutyric acid; SLAM, signaling lymphocyte activation molecule.

a

Only the probe with the highest fold difference for a given gene is reported. Only probe sets with adequate annotation are included. The complete list of probe sets is reported in eTable 1 in the Supplement.