Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
C |
A |
9: 54,516,381 (GRCm39) |
A667S |
probably benign |
Het |
Ank2 |
G |
A |
3: 126,735,621 (GRCm39) |
|
probably benign |
Het |
Arhgef28 |
A |
G |
13: 98,102,038 (GRCm39) |
L812P |
possibly damaging |
Het |
Armc5 |
C |
T |
7: 127,839,470 (GRCm39) |
R263* |
probably null |
Het |
Cadps2 |
A |
T |
6: 23,302,491 (GRCm39) |
V740E |
probably damaging |
Het |
Cckbr |
T |
C |
7: 105,084,103 (GRCm39) |
V279A |
probably benign |
Het |
Cd101 |
T |
C |
3: 100,911,018 (GRCm39) |
D880G |
probably damaging |
Het |
Cep350 |
A |
T |
1: 155,804,297 (GRCm39) |
S929T |
probably benign |
Het |
Chaf1b |
G |
A |
16: 93,702,853 (GRCm39) |
R556H |
probably benign |
Het |
Csn1s1 |
A |
T |
5: 87,822,882 (GRCm39) |
Q69L |
possibly damaging |
Het |
Dennd1b |
T |
C |
1: 138,981,155 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
C |
12: 118,162,503 (GRCm39) |
D22G |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,670,836 (GRCm39) |
H472R |
probably benign |
Het |
Dnah7b |
G |
A |
1: 46,158,428 (GRCm39) |
R337H |
probably benign |
Het |
Eif2ak3 |
T |
C |
6: 70,869,386 (GRCm39) |
V691A |
possibly damaging |
Het |
Ern2 |
T |
C |
7: 121,785,369 (GRCm39) |
R3G |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,828,096 (GRCm39) |
|
probably null |
Het |
Fnbp4 |
T |
C |
2: 90,575,858 (GRCm39) |
F20L |
unknown |
Het |
Gtf2b |
C |
A |
3: 142,484,016 (GRCm39) |
D63E |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,217,243 (GRCm39) |
Y1377C |
probably damaging |
Het |
Klf1 |
A |
G |
8: 85,628,724 (GRCm39) |
T41A |
possibly damaging |
Het |
Lce3d |
G |
A |
3: 92,865,541 (GRCm39) |
S52N |
unknown |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,050,135 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
A |
C |
7: 27,008,369 (GRCm39) |
V1313G |
probably damaging |
Het |
Morc1 |
C |
A |
16: 48,300,208 (GRCm39) |
S235* |
probably null |
Het |
Mr1 |
T |
G |
1: 155,005,014 (GRCm39) |
*342S |
probably null |
Het |
Muc21 |
C |
A |
17: 35,934,118 (GRCm39) |
|
probably benign |
Het |
Nol4l |
T |
A |
2: 153,253,684 (GRCm39) |
S630C |
probably benign |
Het |
Nr4a3 |
C |
T |
4: 48,051,486 (GRCm39) |
P80L |
probably benign |
Het |
Or51a43 |
A |
G |
7: 103,717,620 (GRCm39) |
I206T |
possibly damaging |
Het |
Otof |
A |
G |
5: 30,528,987 (GRCm39) |
V1807A |
probably damaging |
Het |
Pde5a |
T |
A |
3: 122,572,681 (GRCm39) |
V354E |
possibly damaging |
Het |
Pmfbp1 |
A |
T |
8: 110,251,823 (GRCm39) |
E355D |
probably damaging |
Het |
Ppp2r2c |
A |
G |
5: 37,084,875 (GRCm39) |
D112G |
probably damaging |
Het |
Prkacb |
A |
T |
3: 146,457,254 (GRCm39) |
I37N |
probably damaging |
Het |
Prox2 |
T |
C |
12: 85,141,348 (GRCm39) |
D285G |
probably benign |
Het |
Ranbp3l |
A |
G |
15: 9,041,792 (GRCm39) |
S61G |
probably benign |
Het |
Rnf214 |
T |
A |
9: 45,802,196 (GRCm39) |
T289S |
probably damaging |
Het |
Rnf217 |
G |
T |
10: 31,381,973 (GRCm39) |
|
probably null |
Het |
Sc5d |
A |
T |
9: 42,166,723 (GRCm39) |
M272K |
probably benign |
Het |
Slco6c1 |
T |
C |
1: 97,000,626 (GRCm39) |
T542A |
possibly damaging |
Het |
Sord |
T |
A |
2: 122,094,536 (GRCm39) |
I308N |
probably damaging |
Het |
Syvn1 |
A |
T |
19: 6,101,214 (GRCm39) |
|
probably benign |
Het |
Trak1 |
T |
C |
9: 121,272,784 (GRCm39) |
V214A |
possibly damaging |
Het |
Trpm5 |
C |
A |
7: 142,638,547 (GRCm39) |
E322* |
probably null |
Het |
Ttf2 |
T |
C |
3: 100,876,831 (GRCm39) |
T17A |
probably damaging |
Het |
Vmn2r53 |
T |
C |
7: 12,316,343 (GRCm39) |
E492G |
probably benign |
Het |
Xndc1 |
T |
C |
7: 101,727,094 (GRCm39) |
V161A |
probably benign |
Het |
|
Other mutations in Tas2r134 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00562:Tas2r134
|
APN |
2 |
51,518,100 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00563:Tas2r134
|
APN |
2 |
51,518,100 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01121:Tas2r134
|
APN |
2 |
51,518,001 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01122:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01128:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01132:Tas2r134
|
APN |
2 |
51,517,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01312:Tas2r134
|
APN |
2 |
51,518,247 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Tas2r134
|
APN |
2 |
51,517,759 (GRCm39) |
nonsense |
probably null |
|
IGL01774:Tas2r134
|
APN |
2 |
51,518,160 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02735:Tas2r134
|
APN |
2 |
51,517,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Tas2r134
|
UTSW |
2 |
51,518,385 (GRCm39) |
missense |
probably benign |
0.00 |
R1205:Tas2r134
|
UTSW |
2 |
51,517,998 (GRCm39) |
missense |
probably benign |
0.00 |
R2267:Tas2r134
|
UTSW |
2 |
51,518,249 (GRCm39) |
missense |
probably benign |
0.01 |
R3736:Tas2r134
|
UTSW |
2 |
51,517,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R5254:Tas2r134
|
UTSW |
2 |
51,517,559 (GRCm39) |
missense |
probably benign |
0.39 |
R5752:Tas2r134
|
UTSW |
2 |
51,517,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Tas2r134
|
UTSW |
2 |
51,517,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Tas2r134
|
UTSW |
2 |
51,517,782 (GRCm39) |
missense |
probably benign |
0.00 |
R6996:Tas2r134
|
UTSW |
2 |
51,517,601 (GRCm39) |
missense |
probably benign |
0.00 |
R7206:Tas2r134
|
UTSW |
2 |
51,518,120 (GRCm39) |
missense |
probably benign |
0.02 |
R7303:Tas2r134
|
UTSW |
2 |
51,518,145 (GRCm39) |
missense |
probably benign |
0.01 |
R7348:Tas2r134
|
UTSW |
2 |
51,518,414 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7479:Tas2r134
|
UTSW |
2 |
51,517,541 (GRCm39) |
missense |
not run |
|
R7575:Tas2r134
|
UTSW |
2 |
51,518,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Tas2r134
|
UTSW |
2 |
51,518,255 (GRCm39) |
missense |
possibly damaging |
0.54 |
R8721:Tas2r134
|
UTSW |
2 |
51,517,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9384:Tas2r134
|
UTSW |
2 |
51,518,034 (GRCm39) |
missense |
probably damaging |
0.97 |
R9622:Tas2r134
|
UTSW |
2 |
51,518,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
|