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Table 1 Genes responsible for inherited deafness (DFN) with neighbouring microsatellite markers used in the subgenome scan.

From: Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

Chromosome

Distance from pter (MB)

Gene

DFN locus

Size of gene (kb)

Flanking markers and kb spanned

1 p36.31

6.4

ESPN

B36

36

D1S253

D1S2731

342

1 p34.3

34.9

GJB3

A2

5

D 1S1570

D1S496

190

1 p34.2

40.9

KCNQ4

A2

55

D1S2706

D1S1188

273

2 p23.3

26.6

OTOF

B9

102

D2S2350

D2S174

112

3 p21.31

46.7

TMIE

B6

9

AC(46.635)

TG(46.779)

144

4 p16.1

6.4

WFS1

A6/A14

33

TCCC(6.457)

D4S431

77

5 q31.3

140.9

DIAPH1

A1

104

D5S2119

D5S2010

254

5 q32

145.7

POU4F3

A15

1

D 5S2099

D5S2033

628

6 p21.32

33.2

COL11A2

A13

30

D6S2414

D6S1701

449

6 q14.1

76.6

MY O6

B37/A22

167

AC (76.528)

GT(76.674)

146

6 q23.2

133.7

EYA4

A10

288

D6S975

D6S1722

517

7 p15.3

24.5

DFN A5

A5

51

D7S2444

D7S2493

477

7 q22.1

102.6

SLC26A5 (Prestin)

B61

93

D7S2509

D7S2504

478

7 q31.1

106.9

SLC26A4 (Pendrin)

B4

57

D7S496

D7S2459

177

8 q22.3

102.6

TFCP2L3

A28

177

D8S521

D8S1046

761

9 q21.13

72.4

TMC1

B7/B11/A36

315

D9S1837

D9S1876

48

9 q32

114.3

WHRN

B31

103

D9S1824

D9S1855

619

10 p12.1

26.4

MY03A

B30

278

D10S2481

D10S1775

60

10 q21.1

56.0

PCDH15

B23

980

D10S546

D10S1642

321

10 q22.1

73.0

CDH23

B12

420

D10S584

D10S1694

152

11 p15.1

17.5

USH1C (Harmonin)

B18

51

D11S902

D11S4138

268

11 q13.5

76.6

MY07A

B2/A11

87

D11S4179

D11S4186

573

11 q23.3

120.5

TECTA

B21/A8/A12

88

D11S4089

D11S4107

60

12 q13.3

55.7

MY O1A

A48

22

D12S1644

D12S1691

1

13 q12.11

19.7

GJB2 (Connexin26)

B1/A3

5

D 13S1316

D13S175

167

13 q12.11

19.7

GJB6 (Connexin31)

B1/A3

9

D 13S1316

D13S175

167

14 q12

30.4

COCH

A9

16

D14S1021

D14S54

256

15 q15.3

41.7

STRC

B16

19

TG(41.690)

TG(41.707)

17

16 p12.2

21.2

CRYM

A40

20

D16S3045

TTA(21.603)

661

16 p12.2

21.6

OTOA

B22

82

D16S3045

TTA(21.603)

661

17 p11.2

18.0

MY015A

B3

71

AC (17.958)

AA T(18.013)

55

17 q25.3

77.1

ACTG1

A20/A26

3

G T(77.007)

CA (77.107)

100

19 q13.33

55.4

MYH14

A4

107

D19S866

D19S904

22

21 q22.13

36.8

CLDN14

B29

20

D21S1252

D21S167

369

21 q22.3

42.7

TMPRSS3

B8/B10

25

D21S1225

GT(43.277)

740

22 q12.3

35.1

MYH9

A1720

107

D22S1173

D22S283

115

22 q13.1

36.4

TRIOBP

B28

89

TG(36.464)

CA (36.494)

30

  1. DFNA loci are DFN loci associated with dominant (A) hearing loss; DFNB loci are DFN loci associated with recessive (B) hearing loss.