Table 3 Homozygous regions and mutations identified in this study.

From: Identifying mutations in Tunisian families with retinal dystrophy

Family ID

Disease

Genotyping Method

Size of homozygous region, in Mb

Chromosome

Gene

DNA mutation

Predicted protein variant

Coverage

Reference sequence

Previously reported

SIFT

Polyphen

F1

Eord

WES

30.4

8q21.3

CNGB3

c.[607C > T];[607C > T]

p.(R203*);(R203*)

26

NM_019098.4

[21]

F2

RP

IROme

16q21

CNGB1

c.[2293C > T];[2293C > T]

p.(R765C); (R765C)

NM_001297.4

This study and [8]

0

1,00

F3

Stargardt

WES

5.8

1p22.1

ABCA4

c.[2345G > A];[2345G > A]

p.(W782*); (W782*)

5

NM_000350.2

[28]

F4

RP

WES

12.2

15q23

NR2E3

c.[932G > A];[932G > A]

p.(R311Q); (R311Q)

24

NM_014249.3

[35]

0.10

0.627

F5

RP

WES

54.1

1p31.3-p31.2

RPE65

c.[544C > T];[544C > T]

p.(H182Y); (H182Y)

36

NM_000329.2

[30]

0

0.872

F6

Eord

WES

18.2

1p31.3-p31.2

RPE65

c.[1129-2A > G];[1129-2A > G]

30

NM_000329.2

This study

F7

RP

IROme

1p31.3-p31.2

RPE65

c.[325C > T];[569T > A]

p.(R91W); (V172D)

NM_000329.2

This study

0.01/0.01

0.997/0.721

F8

RP

WES

9

4p15.32

PROM1

c.[1354dupT];[1354dupT]

p.(Y452fs*12); (Y452fs*12)

12

NM_001145848.1

[42]

F9

LCA

WES

58

6q12

EYS

c.[5928-2A > G];[5928-2A > G]

24

NM_001292009.1

[23]

F10

RP

IROme

4p16.3

PDE6B

c.[1010A > G];[1010A > G]

p.(H337R); (H337R)

NM_001145291.1

This study and [8]

1.00

0.046

F11

RP

WES

13

2p15

FAM161A

c.[678_681delGAAG]; [678_681delGAAG]

p.(K227Nfs*17); (K227Nfs*17)

94

NM_001201543

This study

F12

RP

WES

8

2q31.3

CERKL

c.[1133 + 3-1133 + 6delAAGT]; [1133 + 3-1133 + 6delAAGT]

21

NM_201548.4

This study

F13

RP

2q31.3

CERKL

c.[1133 + 3-1133 + 6delAAGT]; [1133 + 3-1133 + 6delAAGT]

NM_201548.4

This study

F14

RP

2q31.3

CERKL

c.[1133 + 3-1133 + 6delAAGT]; [1133 + 3-1133 + 6delAAGT]

NM_201548.4

This study

F15

RP

2q31.3

CERKL

c.[1133 + 3-1133 + 6delAAGT]; [1133 + 3-1133 + 6delAAGT]

NM_201548.4

This study