Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,667,189 (GRCm39) |
W221R |
unknown |
Het |
Ank2 |
A |
G |
3: 126,722,454 (GRCm39) |
F1000L |
possibly damaging |
Het |
Aoc1l2 |
T |
C |
6: 48,909,479 (GRCm39) |
F575L |
possibly damaging |
Het |
Bahcc1 |
T |
C |
11: 120,159,126 (GRCm39) |
|
probably benign |
Het |
BC024139 |
T |
C |
15: 76,004,520 (GRCm39) |
M679V |
probably benign |
Het |
Carmil2 |
A |
G |
8: 106,417,952 (GRCm39) |
|
probably benign |
Het |
Catsperg2 |
A |
G |
7: 29,424,904 (GRCm39) |
|
probably benign |
Het |
Chrnb4 |
A |
T |
9: 54,942,812 (GRCm39) |
I154K |
probably damaging |
Het |
Clec2e |
A |
C |
6: 129,071,989 (GRCm39) |
L130W |
probably damaging |
Het |
Coro2b |
G |
T |
9: 62,336,243 (GRCm39) |
Y281* |
probably null |
Het |
Dlk2 |
A |
G |
17: 46,613,903 (GRCm39) |
Y386C |
probably benign |
Het |
Dnah7a |
A |
T |
1: 53,659,882 (GRCm39) |
F709I |
probably benign |
Het |
Efcab3 |
A |
C |
11: 104,997,230 (GRCm39) |
E140A |
probably damaging |
Het |
Exoc1 |
T |
C |
5: 76,706,854 (GRCm39) |
L467P |
probably damaging |
Het |
Fkbp2 |
A |
G |
19: 6,955,980 (GRCm39) |
V75A |
probably benign |
Het |
Glud1 |
T |
C |
14: 34,056,237 (GRCm39) |
F304L |
probably benign |
Het |
Gsr |
T |
A |
8: 34,175,627 (GRCm39) |
V291E |
probably benign |
Het |
Itprid2 |
C |
T |
2: 79,473,815 (GRCm39) |
R189* |
probably null |
Het |
Kap |
A |
G |
6: 133,828,763 (GRCm39) |
|
probably benign |
Het |
Kmt2a |
G |
T |
9: 44,759,689 (GRCm39) |
T720N |
probably damaging |
Het |
Lrrtm4 |
T |
C |
6: 79,999,071 (GRCm39) |
I161T |
probably benign |
Het |
Lyst |
T |
A |
13: 13,831,466 (GRCm39) |
L1630* |
probably null |
Het |
Med13l |
A |
G |
5: 118,885,510 (GRCm39) |
S1488G |
probably benign |
Het |
Mlxip |
A |
G |
5: 123,578,124 (GRCm39) |
K147E |
probably damaging |
Het |
Nalcn |
T |
C |
14: 123,558,899 (GRCm39) |
E810G |
possibly damaging |
Het |
Or2d4 |
A |
G |
7: 106,544,125 (GRCm39) |
F28L |
possibly damaging |
Het |
Or56a5 |
G |
A |
7: 104,793,473 (GRCm39) |
S15F |
probably benign |
Het |
Or5p54 |
T |
C |
7: 107,554,688 (GRCm39) |
V280A |
possibly damaging |
Het |
Pcare |
A |
G |
17: 72,057,266 (GRCm39) |
S804P |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,144,609 (GRCm39) |
|
probably benign |
Het |
Serpina3j |
G |
A |
12: 104,285,960 (GRCm39) |
A372T |
possibly damaging |
Het |
Slc28a3 |
G |
A |
13: 58,722,063 (GRCm39) |
Q274* |
probably null |
Het |
Stk36 |
T |
C |
1: 74,662,511 (GRCm39) |
F543S |
possibly damaging |
Het |
Tfrc |
T |
C |
16: 32,448,930 (GRCm39) |
S690P |
probably damaging |
Het |
Tg |
C |
A |
15: 66,555,647 (GRCm39) |
Q780K |
probably damaging |
Het |
Top1 |
T |
A |
2: 160,557,653 (GRCm39) |
H578Q |
probably damaging |
Het |
Treh |
A |
G |
9: 44,596,634 (GRCm39) |
T463A |
possibly damaging |
Het |
Treml1 |
G |
A |
17: 48,673,016 (GRCm39) |
|
probably benign |
Het |
Trpm2 |
A |
G |
10: 77,753,568 (GRCm39) |
V1312A |
probably benign |
Het |
Ttc41 |
T |
A |
10: 86,612,683 (GRCm39) |
*1319K |
probably null |
Het |
Tulp2 |
A |
G |
7: 45,171,282 (GRCm39) |
I354M |
probably damaging |
Het |
Ugt2b35 |
T |
C |
5: 87,155,254 (GRCm39) |
L363P |
probably damaging |
Het |
Usp13 |
A |
T |
3: 32,956,218 (GRCm39) |
M496L |
probably benign |
Het |
Virma |
T |
C |
4: 11,527,669 (GRCm39) |
S1187P |
possibly damaging |
Het |
Wdr76 |
T |
A |
2: 121,372,951 (GRCm39) |
C593S |
probably damaging |
Het |
Zfp446 |
G |
A |
7: 12,713,252 (GRCm39) |
A97T |
probably damaging |
Het |
|
Other mutations in Scgb2b7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01994:Scgb2b7
|
APN |
7 |
31,403,409 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03252:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03261:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03280:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03302:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03388:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03411:Scgb2b7
|
APN |
7 |
31,404,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Scgb2b7
|
UTSW |
7 |
31,403,437 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7741:Scgb2b7
|
UTSW |
7 |
31,404,454 (GRCm39) |
critical splice donor site |
probably null |
|
R8925:Scgb2b7
|
UTSW |
7 |
31,404,602 (GRCm39) |
missense |
probably benign |
0.00 |
R8927:Scgb2b7
|
UTSW |
7 |
31,404,602 (GRCm39) |
missense |
probably benign |
0.00 |
R9801:Scgb2b7
|
UTSW |
7 |
31,404,580 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1186:Scgb2b7
|
UTSW |
7 |
31,404,547 (GRCm39) |
missense |
probably benign |
0.13 |
Z1186:Scgb2b7
|
UTSW |
7 |
31,404,489 (GRCm39) |
missense |
probably benign |
|
|