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Table 1 Identified arthritis-related gene clusters by transcriptome mapping

From: Identification of arthritis-related gene clusters by microarray analysis of two independent mouse models for rheumatoid arthritis

ID

Chr.

Position (Mb)

nof genes

* nof total genes

Included gene families

1

17

33

10

48

MHC class II

2

17

34

8

67

Complement

3

17

35

2

40

MHC class I

 

17

33–35

20

155

MHC class II/Complement/MHC class I

4

11

81

3

10

CC chemokine ligand

5

11

82

5

25

Schlafen

6

11

83

3

23

CC chemokine ligand

 

11

81–83

11

58

Schlafen/CC chemokine ligand

7

6

68

3

19

Immunoglobulin kappa chain

8

6

69

4

16

Immunoglobulin kappa chain

9

6

70

2

13

Immunoglobulin kappa chain

 

6

68–70

9

48

Immunoglobulin kappa chain

10

12

112

4

8

Immunoglobulin heavy chain

11

12

113

2

3

Immunoglobulin heavy chain

 

12

112–113

6

11

Immunoglobulin heavy chain

12

6

124

5

23

Complement/C-type lectin superfamily

13

15

79

5

27

Colony stimulating factor 2 receptor, beta

14

19

11

5

32

Membrane spanning four-domain, subfamily A

15

2

165

4

32

-

16

3

146

4

10

Guanylate nucleotide binding protein

17

17

17

4

11

Formyl peptide receptor

18

19

5

4

45

-

19

1

75

3

15

-

20

1

167

3

16

Selectin

21

1

174

3

20

(Fc receptor)

22

2

91

3

26

-

23

2

129

3

18

-

24

4

131

3

18

-

25

5

136

3

38

-

26

7

3

3

28

Paired-Ig-like receptor

27

7

37

3

46

-

28

7

39

3

29

Serum amyloid A

29

7

120

3

30

-

30

9

126

3

15

CC chemokine receptor

31

11

70

3

30

-

32

11

102

3

37

-

33

11

114

3

33

-

34

11

117

3

23

-

35

15

105

3

25

-

36

19

12

3

33

-

37

X

63

3

40

-

  1. *Numbers of total genes in the corresponding 1 megabase were obtained from a Mouse Genome Search in The Bioinformatics Analytical Toolkit [20]. CC, Cysteine-Cysteine type; Chr., chromosome; Fc, Fragment crystallizable; ID, identification number; Ig, immunoglobulin; Mb, megabase; MHC, major histocompatibility complex.