Table 2 Gene and RNA editing variants identified by RNA-Seq between depressed patients (DEP, n = 26) and controls (CTRL, n = 31) in the discovery cohort.

From: A game changer for bipolar disorder diagnosis using RNA editing-based biomarkers

Ensembl ID

GeneName

Region

Chr

Position (GRCh38)

Coverage

Editing CTRL

Editing DEP

Fold change

Fold median

P value

AUC ROC

ENSG00000183049

CAMK1D

intron

10

12378385

46

17

21

1.28

1.33

2.20E–03

0.796

ENSG00000033327

GAB2

intron

11

78330944

37

17

24

1.43

1.52

3.71E–03

0.896

ENSG00000142166

IFNAR1

3UTR

21

33355807

32

17

24

1.42

1.24

1.21E–02

0.910

ENSG00000157551

KCNJ15

intron

21

38287526

85

22

18

0.83

0.75

1.85E–02

0.737

ENSG00000166501

LYN

3UTR

8

56012553

44

15

20

1.35

1.33

4.37E–03

0.774

ENSG00000135679

MDM2

intron

12

68821612

36

12

16

1.29

1.29

2.89E–02

0.797

ENSG00000166501

PRKCB

intron

16

23920896

78

16

12

0.74

0.69

3.43E–03

0.853

  1. Shown are the gene ID, gene name, chromosome and information on the genomic localization of detected editing sites. The position (GRCh38) of editing site identified in RNA Seq study and its Coverage, Mean editing values by conditions (in percentage), Fold Change, Fold Median, p value and AUC ROC are indicated.