Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
G |
2: 68,571,881 (GRCm39) |
T586A |
probably benign |
Het |
Acads |
G |
T |
5: 115,250,874 (GRCm39) |
T141N |
probably benign |
Het |
Ankmy1 |
C |
T |
1: 92,808,745 (GRCm39) |
R721H |
probably damaging |
Het |
Appl1 |
A |
G |
14: 26,672,665 (GRCm39) |
V236A |
possibly damaging |
Het |
Arhgef5 |
C |
T |
6: 43,249,869 (GRCm39) |
Q207* |
probably null |
Het |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
Atp6v0a2 |
G |
T |
5: 124,789,426 (GRCm39) |
|
probably benign |
Het |
Cenpf |
T |
C |
1: 189,384,670 (GRCm39) |
K2537E |
possibly damaging |
Het |
Cox7a1 |
A |
T |
7: 29,884,562 (GRCm39) |
E32V |
possibly damaging |
Het |
Dis3 |
A |
T |
14: 99,336,221 (GRCm39) |
M95K |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,289,193 (GRCm39) |
|
probably benign |
Het |
Dock10 |
T |
A |
1: 80,551,840 (GRCm39) |
Y665F |
probably damaging |
Het |
Dynlt5 |
C |
A |
4: 102,845,803 (GRCm39) |
Q12K |
probably benign |
Het |
Ghsr |
A |
T |
3: 27,429,004 (GRCm39) |
Q343L |
probably benign |
Het |
Gm3252 |
T |
A |
14: 4,746,353 (GRCm38) |
V215E |
probably damaging |
Het |
Gm9979 |
A |
G |
13: 40,859,225 (GRCm39) |
|
noncoding transcript |
Het |
Grik2 |
A |
T |
10: 48,977,331 (GRCm39) |
M867K |
probably benign |
Het |
Grm7 |
A |
G |
6: 111,335,919 (GRCm39) |
T777A |
probably damaging |
Het |
Hc |
T |
A |
2: 34,890,886 (GRCm39) |
Q1310L |
possibly damaging |
Het |
Ifi44 |
A |
G |
3: 151,451,492 (GRCm39) |
F205L |
probably damaging |
Het |
Igkv4-86 |
T |
C |
6: 68,887,617 (GRCm39) |
I40V |
probably benign |
Het |
Jag1 |
T |
C |
2: 136,957,505 (GRCm39) |
D69G |
possibly damaging |
Het |
Lrch1 |
T |
C |
14: 75,051,138 (GRCm39) |
D333G |
probably damaging |
Het |
Mapre3 |
T |
A |
5: 31,022,053 (GRCm39) |
I187N |
probably damaging |
Het |
Myo15b |
T |
C |
11: 115,777,337 (GRCm39) |
|
probably null |
Het |
Nanos2 |
C |
T |
7: 18,721,794 (GRCm39) |
P89S |
probably damaging |
Het |
Or4c109 |
T |
A |
2: 88,818,424 (GRCm39) |
M41L |
probably benign |
Het |
Parp16 |
G |
A |
9: 65,141,098 (GRCm39) |
V223I |
probably damaging |
Het |
Rnf123 |
A |
G |
9: 107,946,947 (GRCm39) |
M231T |
probably benign |
Het |
Suco |
C |
A |
1: 161,676,322 (GRCm39) |
|
probably benign |
Het |
Synj1 |
G |
T |
16: 90,773,584 (GRCm39) |
T459N |
probably benign |
Het |
Taf4b |
C |
T |
18: 14,975,040 (GRCm39) |
Q732* |
probably null |
Het |
Tll1 |
C |
T |
8: 64,500,031 (GRCm39) |
|
probably benign |
Het |
Vmn1r168 |
A |
G |
7: 23,240,916 (GRCm39) |
I258V |
probably benign |
Het |
Vmn2r71 |
T |
A |
7: 85,273,535 (GRCm39) |
M783K |
probably damaging |
Het |
Vmn2r98 |
G |
A |
17: 19,301,223 (GRCm39) |
V742I |
probably benign |
Het |
|
Other mutations in Tas2r102 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00685:Tas2r102
|
APN |
6 |
132,739,488 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01777:Tas2r102
|
APN |
6 |
132,739,815 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01956:Tas2r102
|
APN |
6 |
132,739,416 (GRCm39) |
nonsense |
probably null |
|
IGL02126:Tas2r102
|
APN |
6 |
132,739,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Tas2r102
|
UTSW |
6 |
132,739,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0573:Tas2r102
|
UTSW |
6 |
132,739,636 (GRCm39) |
missense |
probably damaging |
0.98 |
R0726:Tas2r102
|
UTSW |
6 |
132,739,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1777:Tas2r102
|
UTSW |
6 |
132,739,254 (GRCm39) |
missense |
probably benign |
0.08 |
R3615:Tas2r102
|
UTSW |
6 |
132,739,781 (GRCm39) |
nonsense |
probably null |
|
R3616:Tas2r102
|
UTSW |
6 |
132,739,781 (GRCm39) |
nonsense |
probably null |
|
R4556:Tas2r102
|
UTSW |
6 |
132,739,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Tas2r102
|
UTSW |
6 |
132,739,642 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4724:Tas2r102
|
UTSW |
6 |
132,739,520 (GRCm39) |
missense |
probably damaging |
0.97 |
R5268:Tas2r102
|
UTSW |
6 |
132,739,360 (GRCm39) |
missense |
probably damaging |
0.98 |
R5494:Tas2r102
|
UTSW |
6 |
132,740,106 (GRCm39) |
missense |
probably benign |
0.12 |
|