Table 2

Haplolethal and haplosterile genes

Gene

Location


X chromosome

RpL36

1B12

RpL35

5A11

RpL17

6C10

RpS6

7C2

Fs(1)10A region

10A4-10

Hdl region

12A7-9

RpL37a

13B1

RpS19a

14F4

RpS5a

15E5-7

wupA region

16F7

RpS10b

18D3

Chromosome arm 2L

dpp

22F1-3

RpL37A

25C4

RpL36A

28D3

RpS13

29B2

RpL13

30F3

RpL7

31B1

RpL9

32C1

RpL24

34B10

Chromosome arm 2R

RpL31

45F5

RpS11

48E8-9

RpS15

53C8

RpL18A

54C3

RpL11

56D7

RpL23

59B3

RpL12a

60B7

RpL39a

60B7

Chromosome arm 3L

RpL23A

62A10

RpL8

62E7

RpL28

63B14

RpL18

65E9

RpL14

66D8

Haplolethal region

67D10-E1

RpS4

69F6

RpL10

80A

Chromosome arm 3R

RpL35A

83A4

RpL13A

83B6-7

Tpl region

83E1-2

RpL34b

85D15

Ms(3)88C region

88C9-10

Su(var)3-9

88E8

Abd-B

89E4-5

RpS3

94E13

RpL27

96E9-10

RpL4

98B6

RpS8

99C4

RpL32

99D3

RpS7

99E2

RpL6

100C7


aA Minute phenotype results from deleting chromosomal region 60B, but it may be associated with haploinsufficiency of RpL12, RpL39 or both genes.

Cook et al. Genome Biology 2012 13:R21   doi:10.1186/gb-2012-13-3-r21

Open Data