Genes |
% Recombination |
Map Units |
|
|
|
Value |
S.E. |
Ref |
Value |
S.E. |
Ref |
Chromosome 4A (VIII) |
4AS |
|
|
|
|
|
|
|
|
|
Adh- B1- |
cent |
20.0 |
3.5 |
{1197} |
21.2 |
4.2 |
. |
|
Hd- |
cent |
7.7 |
3.7 |
{1195} |
. |
. |
. |
|
|
|
|
|
|
|
|
|
4AL |
|
|
|
|
|
|
|
|
|
cent- |
Lr30 |
2.9 |
1.3 |
{315} |
. |
. |
. |
|
cent- |
Lr28 |
39.2 |
2.7 |
{967} |
52.8 |
7.0 |
. |
|
Sr7a- |
Hd |
I |
. |
{671} |
. |
. |
. |
|
|
|
|
|
|
|
|
|
Chromosome 4B {IV} |
4BS |
|
|
|
|
|
|
|
|
|
ms1b- |
cent |
I |
. |
{064} |
. |
. |
. |
|
ms1b- |
Lr25 |
34 |
. |
{064} |
41.5 |
. |
. |
|
ms1c- |
cent |
I |
. |
{064} |
. |
. |
. |
|
ms1c- |
Lr25 |
20 |
. |
{064} |
21.0 |
. |
. |
|
Adh-Ala- |
Gai/Rht-B1 |
23.1 |
4.0 |
{1442} |
25.0 |
5.1 |
. |
|
Gai1- |
Gai3 |
0 |
. |
{406} |
. |
. |
. |
|
Rht-B1/Gai1 |
cent |
15 |
3 |
{980} |
. |
. |
. |
|
Rht-B1- |
ß-Amy-A1 |
I |
. |
{008} |
. |
. |
. |
.. |
@ß-Amy-A1 - |
cent |
>35 |
{008} |
43.4 |
. |
. |
. |
|
pa- |
H1 |
. |
. |
. |
29 |
2.6 |
{921} |
|
Hl - |
Pa |
. |
. |
. |
30 |
. |
{042} |
Gene order: @ Adh - Rht-B1 - cent {1442}. |
|
|
|
|
|
|
|
|
|
4BL |
|
|
|
|
|
|
|
|
|
cent- |
Lr25/Pm7 |
1 |
. |
{271} |
. |
. |
. |
|
cent- |
Hp |
30 |
. |
{275} |
34.7 |
. |
. |
|
cent- |
ß-Amy-A1 |
35 |
. |
{008} |
43 |
. |
. |
|
Lr25- |
Pm7 |
0 |
. |
{271} |
. |
. |
. |
|
Rht1- |
ß-Amy-A1 |
I |
. |
{008} |
. |
. |
. |
|
|
|
|
|
|
|
|
|
Chromosome 4D |
4DS |
|
|
|
|
|
|
|
|
|
Ms2- |
Rht10 |
0.005 |
. |
{805} |
. |
. |
. |
|
Ms2- |
cent |
31.2 |
. |
{807,806} |
36.5 |
. |
. |
|
Rht2/Gai2 - |
cent |
13 |
4 |
{980} |
. |
. |
. |
|
|
|
|
|
|
|
|
|
According to {805}, Ms2 and Rht10
were closely linked. However, a translocated recombinant male sterile dwarf
was isolated. |
Gibberellic insensitivity in Ai-Bian 1 possessing
Rht10
was allelic with Rht2 {114}. It is therefore likely that Rht10
and Rht2 are allelic. |
|
|
|
|
|
|
|
|
|
4DL |
|
|
|
|
|
|
|
|
|
Rht2- |
ß-Amy-D1 |
I |
. |
{008} |
. |
. |
. |
|
@ cent- |
ß-Amy-D1 |
>35 |
. |
{008} |
>43.4 |
. |
. |
|
Alt2- |
Kna1 |
. |
. |
. |
12.5 |
. |
{848} |
|
|
|
|
|
|
|
|
|