Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
T |
A |
2: 151,315,466 (GRCm39) |
M71L |
probably benign |
Het |
Abcb11 |
A |
G |
2: 69,154,169 (GRCm39) |
|
probably benign |
Het |
Ago4 |
T |
C |
4: 126,410,645 (GRCm39) |
T249A |
probably benign |
Het |
Ahr |
A |
T |
12: 35,562,922 (GRCm39) |
C92* |
probably null |
Het |
Arhgap17 |
G |
A |
7: 122,885,996 (GRCm39) |
|
probably benign |
Het |
Arid1a |
G |
T |
4: 133,420,126 (GRCm39) |
T992K |
unknown |
Het |
Camk2a |
A |
G |
18: 61,111,061 (GRCm39) |
I83M |
probably damaging |
Het |
Ccdc154 |
T |
C |
17: 25,386,792 (GRCm39) |
|
probably null |
Het |
Chtf18 |
T |
C |
17: 25,941,177 (GRCm39) |
H607R |
possibly damaging |
Het |
Col25a1 |
T |
C |
3: 130,313,422 (GRCm39) |
|
probably benign |
Het |
Col9a1 |
C |
T |
1: 24,276,574 (GRCm39) |
Q530* |
probably null |
Het |
Cryl1 |
G |
T |
14: 57,523,904 (GRCm39) |
D219E |
probably damaging |
Het |
Cul3 |
A |
T |
1: 80,300,781 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
A |
17: 46,851,301 (GRCm39) |
R373L |
probably benign |
Het |
Exo1 |
A |
G |
1: 175,721,309 (GRCm39) |
Y316C |
possibly damaging |
Het |
Fam114a1 |
G |
A |
5: 65,187,465 (GRCm39) |
V408M |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,347,185 (GRCm39) |
S4792C |
possibly damaging |
Het |
Hps5 |
A |
G |
7: 46,432,940 (GRCm39) |
F260S |
probably damaging |
Het |
Hrh4 |
T |
C |
18: 13,155,477 (GRCm39) |
S339P |
probably benign |
Het |
Ist1 |
A |
T |
8: 110,405,584 (GRCm39) |
L152Q |
probably damaging |
Het |
Marco |
A |
G |
1: 120,418,683 (GRCm39) |
V190A |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,709,364 (GRCm39) |
V1711A |
probably benign |
Het |
Mmp9 |
A |
G |
2: 164,791,644 (GRCm39) |
Y179C |
probably damaging |
Het |
Mrgprb5 |
A |
G |
7: 47,818,742 (GRCm39) |
|
probably benign |
Het |
Mrgprx1 |
G |
T |
7: 47,671,371 (GRCm39) |
C125* |
probably null |
Het |
Msh6 |
A |
G |
17: 88,298,234 (GRCm39) |
|
probably benign |
Het |
Myot |
C |
A |
18: 44,488,177 (GRCm39) |
R441S |
probably benign |
Het |
Paf1 |
A |
G |
7: 28,098,115 (GRCm39) |
|
probably benign |
Het |
Pde11a |
A |
G |
2: 75,821,606 (GRCm39) |
L891P |
probably damaging |
Het |
Prkar2a |
T |
A |
9: 108,596,460 (GRCm39) |
I135N |
probably damaging |
Het |
Rap1gap |
C |
T |
4: 137,454,355 (GRCm39) |
T646M |
probably damaging |
Het |
Rgs7bp |
T |
C |
13: 105,088,087 (GRCm39) |
D229G |
possibly damaging |
Het |
Rhobtb3 |
C |
T |
13: 76,025,547 (GRCm39) |
S523N |
probably damaging |
Het |
Setd7 |
A |
T |
3: 51,428,826 (GRCm39) |
Y335N |
probably damaging |
Het |
Setdb2 |
C |
T |
14: 59,639,764 (GRCm39) |
R709Q |
probably damaging |
Het |
Socs4 |
T |
C |
14: 47,528,264 (GRCm39) |
Y400H |
probably damaging |
Het |
Spag16 |
A |
T |
1: 69,909,479 (GRCm39) |
H192L |
probably damaging |
Het |
Ssh1 |
A |
T |
5: 114,084,541 (GRCm39) |
C566* |
probably null |
Het |
Stap1 |
T |
G |
5: 86,234,552 (GRCm39) |
I98S |
possibly damaging |
Het |
Tgs1 |
C |
T |
4: 3,585,836 (GRCm39) |
H238Y |
probably damaging |
Het |
Tifab |
T |
C |
13: 56,324,275 (GRCm39) |
Y56C |
probably benign |
Het |
Tssk2 |
A |
G |
16: 17,717,653 (GRCm39) |
E352G |
probably benign |
Het |
Vmn2r57 |
A |
T |
7: 41,049,874 (GRCm39) |
V625D |
probably benign |
Het |
Wbp1l |
T |
C |
19: 46,632,876 (GRCm39) |
Y75H |
probably benign |
Het |
Wnt5a |
T |
C |
14: 28,228,077 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or11g7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01663:Or11g7
|
APN |
14 |
50,690,607 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02663:Or11g7
|
APN |
14 |
50,691,309 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02858:Or11g7
|
APN |
14 |
50,690,507 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02955:Or11g7
|
APN |
14 |
50,691,442 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03210:Or11g7
|
APN |
14 |
50,691,440 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03249:Or11g7
|
APN |
14 |
50,690,668 (GRCm39) |
missense |
probably damaging |
0.98 |
G1Funyon:Or11g7
|
UTSW |
14 |
50,691,021 (GRCm39) |
missense |
probably benign |
0.08 |
R0946:Or11g7
|
UTSW |
14 |
50,691,130 (GRCm39) |
missense |
probably benign |
0.13 |
R1449:Or11g7
|
UTSW |
14 |
50,691,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Or11g7
|
UTSW |
14 |
50,690,634 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1465:Or11g7
|
UTSW |
14 |
50,690,634 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1513:Or11g7
|
UTSW |
14 |
50,691,138 (GRCm39) |
missense |
probably benign |
0.00 |
R1908:Or11g7
|
UTSW |
14 |
50,691,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R2422:Or11g7
|
UTSW |
14 |
50,690,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Or11g7
|
UTSW |
14 |
50,690,653 (GRCm39) |
missense |
probably benign |
0.14 |
R4184:Or11g7
|
UTSW |
14 |
50,690,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Or11g7
|
UTSW |
14 |
50,690,874 (GRCm39) |
missense |
probably damaging |
0.96 |
R5028:Or11g7
|
UTSW |
14 |
50,691,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Or11g7
|
UTSW |
14 |
50,691,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R6057:Or11g7
|
UTSW |
14 |
50,691,201 (GRCm39) |
nonsense |
probably null |
|
R6455:Or11g7
|
UTSW |
14 |
50,691,042 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6903:Or11g7
|
UTSW |
14 |
50,691,412 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6998:Or11g7
|
UTSW |
14 |
50,690,890 (GRCm39) |
missense |
probably benign |
0.29 |
R7671:Or11g7
|
UTSW |
14 |
50,691,342 (GRCm39) |
missense |
probably benign |
0.04 |
R8048:Or11g7
|
UTSW |
14 |
50,691,373 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8301:Or11g7
|
UTSW |
14 |
50,691,021 (GRCm39) |
missense |
probably benign |
0.08 |
X0066:Or11g7
|
UTSW |
14 |
50,691,115 (GRCm39) |
missense |
probably benign |
0.00 |
|