Skip to main content
. 2019 Feb 20;9:2399. doi: 10.1038/s41598-019-38643-2

Table 2.

Enriched pathways in cxcr4b −/− neutrophils (analysis performed with DESeq2 paired).

DESEq2 paired
Gene ID Gene symbol Gene name LogFC p
Focal adhesion/ECM-receptor interaction
ENSDARG00000032639 cd36 CD36 molecule (thrombospondin receptor) −1.3 8.3E-03
ENSDARG00000012405 col1a1a collagen, type I, alpha 1a 0.8 2.2E-02
ENSDARG00000061436 col6a2 collagen, type VI, alpha 2 1.0 4.5E-02
ENSDARG00000074316 itga1 integrin, alpha 1 1.1 8.8E-03
ENSDARG00000103056 itga4 integrin alpha 4 0.8 2.6E-02
ENSDARG00000020785 lama4 laminin, alpha 4 1.1 7.1E-03
ENSDARG00000093572 lamc3 laminin, gamma 3 1.5 5.2E-03
ENSDARG00000060711 sv2bb synaptic vesicle glycoprotein 2Bb 1.7 3.4E-03
ENSDARG00000008867 rap1b RAP1B, member of RAS oncogene family −0.9 2.1E-02
ENSDARG00000007825 map2k1 mitogen-activated protein kinase kinase 1 −1.1 2.1E-02
ENSDARG00000098578 pdgfab platelet-derived growth factor alpha polypeptide b −1.0 2.1E-02
Cardiac muscle contraction
ENSDARG00000007739 atp1a1a.2 ATPase, Na+/K+ transporting, alpha 1a polypeptide −1.6 5.8E-05
ENSDARG00000018259 atp1a3a ATPase, Na+/K+ transporting, alpha 3a polypeptide 0.9 9.6E-03
ENSDARG00000076833 atp1b1b ATPase, Na+/K+ transporting, beta 1b polypeptide −1.5 4.0E-04
ENSDARG00000063905 mt-co1 cytochrome c oxidase I, mitochondrial −0.7 9.3E-03
ENSDARG00000063908 mt-co2 cytochrome c oxidase II, mitochondrial −0.6 4.1E-02
ENSDARG00000063911 mt-atp6 ATP synthase 6, mitochondrial −0.7 2.0E-02
ENSDARG00000063912 mt-co3 cytochrome c oxidase III, mitochondrial −0.7 1.7E-02
ENSDARG00000023886 cacna2d4b calcium channel, voltage-dependent, alpha 2/delta subunit 4b 1.2 3.2E-02
ENSDARG00000045230 cox6b1 cytochrome c oxidase subunit VIb polypeptide 1 −1.2 4.2E-03
ENSDARG00000038075 cyc1 cytochrome c-1 −0.7 1.9E-02
ENSDARG00000079564 vmhc ventricular myosin heavy chain 2.1 3.7E-05
Axon guidance
ENSDARG00000044029 efnb3a ephrin-B3a 1.2 3.2E-02
MAPK signaling pathway
ENSDARG00000008867 rap1b RAP1B, member of RAS oncogene family −0.9 2.1E-02
ENSDARG00000035535 rasa1a RAS p21 protein activator (GTPase activating protein) 1a 0.8 4.5E-02
ENSDARG00000005482 rapgef2 Rap guanine nucleotide exchange factor (GEF) 2 1.0 9.9E-03
ENSDARG00000043241 arrb1 arrestin, beta 1 1.3 3.1E-02
ENSDARG00000023886 cacna2d4b calcium channel, voltage-dependent, alpha 2/delta subunit 4b 1.2 3.2E-02
ENSDARG00000102474 dusp16 dual specificity phosphatase 16 1.4 9.6E-04
ENSDARG00000061255 dusp3a dual specificity phosphatase 3a 1.4 1.5E-02
ENSDARG00000009299 dusp8a dual specificity phosphatase 8a 1.0 3.0E-03
ENSDARG00000092281 FLNB filamin B 1.3 2.1E-02
ENSDARG00000007825 map2k1 mitogen-activated protein kinase kinase 1 −1.1 2.1E-02
ENSDARG00000001234 map4k2 mitogen-activated protein kinase kinase kinase kinase 2 −1.2 2.9E-02
ENSDARG00000071357 map4k3b mitogen-activated protein kinase kinase kinase kinase 3b 1.3 3.2E-03
ENSDARG00000070454 pla2g12a phospholipase A2, group XIIA −1.4 1.4E-02
ENSDARG00000015662 pla2g12b phospholipase A2, group XIIB −1.4 1.4E-02
ENSDARG00000098578 pdgfab platelet-derived growth factor alpha polypeptide b −1.0 2.1E-02
ENSDARG00000060551 rps6ka5 ribosomal protein S6 kinase, polypeptide 5 1.5 8.7E-04
ENSDARG00000017494 tgfbr1a transforming growth factor, beta receptor 1a 1.2 4.1E-02

Pathway analysis in Cxcr4b-deficient neutrophils. Genes selected with DESeq (p < 0.05) and edgeR (p < 0.05) analyses in RStudio (from 21621 to 615 genes) were converted to the human orthologues using g:PROFILER and uploaded in DAVID Bioinformatics Resources 6.7 for pathway analysis. Up-regulation of genes involved in focal adhesion/ECM-Receptor interaction and axon guidance was identified, whereas down-regulation of genes in the metabolism of xenobiotic by P450 was found. Additional analysis was performed using DESeq2 paired (Table 2). The same pathways were identified with DESeq/edgeR (Table 1) and DESeq2 paired (Table 2) and the genes listed in Table 2 were in addition to genes described in Table 1. Enriched pathways indicate alteration in motility, as shown by the analysis performed with DESeq and edgeR and reveal members of the MAPK signaling to be differentially expressed.