Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
A |
T |
1: 53,197,928 (GRCm39) |
L140Q |
probably damaging |
Het |
Abca8b |
A |
T |
11: 109,848,027 (GRCm39) |
M756K |
probably benign |
Het |
Cd44 |
T |
C |
2: 102,731,687 (GRCm39) |
D2G |
probably damaging |
Het |
Cdan1 |
T |
C |
2: 120,556,224 (GRCm39) |
I681V |
probably benign |
Het |
Cdc5l |
C |
T |
17: 45,721,816 (GRCm39) |
A485T |
probably benign |
Het |
Cfh |
T |
C |
1: 140,047,664 (GRCm39) |
I488M |
possibly damaging |
Het |
Cntn2 |
T |
A |
1: 132,453,634 (GRCm39) |
L346F |
probably damaging |
Het |
Creb3l2 |
T |
C |
6: 37,311,484 (GRCm39) |
H435R |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,675,932 (GRCm39) |
|
probably benign |
Het |
Fam162a |
C |
T |
16: 35,864,451 (GRCm39) |
R38K |
probably benign |
Het |
Fat1 |
A |
T |
8: 45,478,518 (GRCm39) |
E2521D |
probably benign |
Het |
Foxo1 |
A |
G |
3: 52,252,583 (GRCm39) |
R249G |
probably damaging |
Het |
Grm6 |
A |
G |
11: 50,744,051 (GRCm39) |
E174G |
probably damaging |
Het |
Gtpbp2 |
G |
A |
17: 46,478,253 (GRCm39) |
R467H |
probably damaging |
Het |
Hypk |
A |
G |
2: 121,284,160 (GRCm39) |
|
probably benign |
Het |
Ifih1 |
T |
C |
2: 62,429,143 (GRCm39) |
T932A |
possibly damaging |
Het |
Igfbp1 |
C |
A |
11: 7,148,091 (GRCm39) |
P45T |
probably damaging |
Het |
Ik |
A |
G |
18: 36,881,943 (GRCm39) |
K142E |
probably damaging |
Het |
Ltbp3 |
T |
C |
19: 5,792,348 (GRCm39) |
L27P |
probably benign |
Het |
Mast3 |
A |
G |
8: 71,233,838 (GRCm39) |
V969A |
probably damaging |
Het |
Mrps24 |
G |
A |
11: 5,654,676 (GRCm39) |
R93* |
probably null |
Het |
Or13a20 |
T |
C |
7: 140,232,033 (GRCm39) |
I47T |
probably damaging |
Het |
Or1j14 |
A |
G |
2: 36,417,426 (GRCm39) |
M1V |
probably null |
Het |
Or7g19 |
T |
C |
9: 18,856,346 (GRCm39) |
V134A |
probably benign |
Het |
Otop2 |
G |
A |
11: 115,220,201 (GRCm39) |
G347D |
probably damaging |
Het |
Pcdhb20 |
A |
G |
18: 37,639,217 (GRCm39) |
E581G |
probably damaging |
Het |
Rnf146 |
T |
C |
10: 29,223,363 (GRCm39) |
I174M |
probably damaging |
Het |
Serpinb9g |
G |
A |
13: 33,679,089 (GRCm39) |
V320I |
probably benign |
Het |
Sh3pxd2b |
G |
T |
11: 32,372,263 (GRCm39) |
A477S |
probably benign |
Het |
Slc23a3 |
T |
G |
1: 75,109,964 (GRCm39) |
|
probably benign |
Het |
Ssrp1 |
T |
G |
2: 84,871,978 (GRCm39) |
Y401D |
probably damaging |
Het |
Tas2r109 |
A |
T |
6: 132,957,148 (GRCm39) |
W261R |
probably damaging |
Het |
Tead1 |
T |
A |
7: 112,475,269 (GRCm39) |
|
probably null |
Het |
Tiam2 |
A |
G |
17: 3,479,255 (GRCm39) |
S663G |
probably benign |
Het |
Trbv20 |
T |
G |
6: 41,165,195 (GRCm39) |
|
probably benign |
Het |
Tspan9 |
T |
C |
6: 128,011,135 (GRCm39) |
I19M |
probably benign |
Het |
Ttbk2 |
T |
A |
2: 120,579,465 (GRCm39) |
E552D |
probably benign |
Het |
Zfp292 |
A |
G |
4: 34,810,863 (GRCm39) |
V727A |
probably damaging |
Het |
|
Other mutations in Tas2r144 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02349:Tas2r144
|
APN |
6 |
42,193,010 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02644:Tas2r144
|
APN |
6 |
42,192,787 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02816:Tas2r144
|
APN |
6 |
42,192,539 (GRCm39) |
missense |
probably benign |
0.03 |
R0375:Tas2r144
|
UTSW |
6 |
42,193,058 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1526:Tas2r144
|
UTSW |
6 |
42,192,674 (GRCm39) |
missense |
probably benign |
|
R1543:Tas2r144
|
UTSW |
6 |
42,192,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1678:Tas2r144
|
UTSW |
6 |
42,192,490 (GRCm39) |
missense |
probably benign |
0.44 |
R1868:Tas2r144
|
UTSW |
6 |
42,192,936 (GRCm39) |
missense |
probably benign |
0.01 |
R1880:Tas2r144
|
UTSW |
6 |
42,193,004 (GRCm39) |
missense |
probably benign |
0.02 |
R5173:Tas2r144
|
UTSW |
6 |
42,193,048 (GRCm39) |
missense |
probably benign |
0.40 |
R6108:Tas2r144
|
UTSW |
6 |
42,192,691 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6249:Tas2r144
|
UTSW |
6 |
42,192,291 (GRCm39) |
nonsense |
probably null |
|
R6533:Tas2r144
|
UTSW |
6 |
42,192,280 (GRCm39) |
missense |
probably benign |
|
R6850:Tas2r144
|
UTSW |
6 |
42,192,857 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7237:Tas2r144
|
UTSW |
6 |
42,192,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Tas2r144
|
UTSW |
6 |
42,192,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R7431:Tas2r144
|
UTSW |
6 |
42,192,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R8206:Tas2r144
|
UTSW |
6 |
42,192,325 (GRCm39) |
missense |
probably damaging |
0.98 |
R9341:Tas2r144
|
UTSW |
6 |
42,193,066 (GRCm39) |
missense |
probably benign |
0.03 |
R9343:Tas2r144
|
UTSW |
6 |
42,193,066 (GRCm39) |
missense |
probably benign |
0.03 |
R9640:Tas2r144
|
UTSW |
6 |
42,192,428 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Tas2r144
|
UTSW |
6 |
42,193,099 (GRCm39) |
missense |
probably damaging |
1.00 |
|