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Table 4 Ingenuity pathway analysis of the 85 co-occurring genes

From: Changes in DNA methylation in naïve T helper cells regulate the pathophysiological state in minimal-change nephrotic syndrome

(a) Top molecules

Genes

Description

Chromosome

Exp. value

SAC3D1

SAC3 domain containing 1

11q13.1

0.772

EIF3B

Eukaryotic translation initiation factor 3, subunit B

7p22.3

0.692

PDF

Peptide deformylase (mitochondrial)

16q22.1

0.680

FKBP1A

FK506 binding protein 1A, 12 kDa

20p13

0.661

TIMP2

TIMP metallopeptidase inhibitor 2

17q25

0.586

RYR3

Ryanodine receptor 3

15q14-q15

0.567

U2AF2

U2 small nuclear RNA auxillary factor 2

19q13.42

0.558

B3GALT6

UDP-Gal:betaGal beta 1, 3-galactosyltransferase polypeptide 6

1p36.33

0.543

CBX7

Chromobox homolog 7

22q13.1

0.536

CDX19

Cyclin-dependent kinase 19

6q21

0.523

(b) Top canonical pathways

Name

P value

Ratio

Insulin receptor signaling

3.45E−03

3/139 (0.022)

Protein kinase A signaling

5.74E−03

4/327 (0.012)

Clarin-mediated endocytosis signalling

6.29E−03

3/172 (0/017)

Spliceosomal cycle

7.06E−03

1/10 (0.100)

Calcium signaling

7.93E−03

3/207 (0.014)