|
Gene
|
Location
|
|---|
|
X chromosome
| |
|
RpL7A
|
6B1
|
|
RpS28b
|
8E7
|
|
RpS15Aa
|
11E11-12
|
|
eIF-2alpha
|
14C6
|
|
Chromosome arm 2L
| |
|
RpLP1
|
21C2
|
|
RpS21
|
23B6
|
|
RpL40
|
24E1
|
|
RpL27A
|
24F3
|
|
RpS27A
|
31E1
|
|
RpS26
|
36F4
|
|
RpL21
|
40A-B
|
|
RpL5
|
40B
|
|
Chromosome arm 2R
| |
|
RpL38
|
41C-E
|
|
RpS23
|
50E4
|
|
RpLP2
|
53C9
|
|
RpS18
|
56F11
|
|
RpS16
|
58F1
|
|
RpS24
|
58F3
|
|
RpL19
|
60E11
|
|
Chromosome arm 3L
| |
|
RpS17
|
67B5
|
|
RpS9
|
67B11
|
|
RpL15
|
80F
|
|
Chromosome arm 3R
| |
|
RpS29
|
85E8
|
|
RpS25
|
86D8
|
|
RpS20a
|
93A1
|
|
RpS30a
|
93A2
|
|
RpS27
|
96C8
|
|
Chromosome 4
| |
|
RpS3A
|
101F1
|
- aA Minute phenotype results from deleting chromosomal region 93A, but it may be associated with haploinsufficiency of RpS20, RpS30 or both genes.
