Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,771,020 (GRCm39) |
H167Q |
probably benign |
Het |
Adamts20 |
T |
C |
15: 94,277,827 (GRCm39) |
T212A |
probably benign |
Het |
Ap3b1 |
C |
A |
13: 94,554,607 (GRCm39) |
L248I |
probably damaging |
Het |
Atl1 |
T |
G |
12: 70,005,973 (GRCm39) |
D426E |
probably benign |
Het |
Cage1 |
T |
A |
13: 38,207,078 (GRCm39) |
I256F |
probably damaging |
Het |
Calcr |
A |
T |
6: 3,708,484 (GRCm39) |
|
probably null |
Het |
Canx |
T |
C |
11: 50,195,265 (GRCm39) |
T268A |
probably benign |
Het |
Chd7 |
A |
T |
4: 8,866,353 (GRCm39) |
M842L |
possibly damaging |
Het |
Clca4a |
T |
C |
3: 144,658,609 (GRCm39) |
T787A |
probably benign |
Het |
Clstn3 |
T |
C |
6: 124,433,939 (GRCm39) |
Y407C |
probably damaging |
Het |
Copa |
C |
A |
1: 171,929,791 (GRCm39) |
T286N |
probably damaging |
Het |
Cyb5a |
G |
A |
18: 84,889,718 (GRCm39) |
R49Q |
possibly damaging |
Het |
Def6 |
A |
G |
17: 28,438,950 (GRCm39) |
K219E |
probably damaging |
Het |
Eif4g1 |
G |
T |
16: 20,497,593 (GRCm39) |
|
probably benign |
Het |
Eif5 |
A |
T |
12: 111,508,183 (GRCm39) |
K161N |
probably benign |
Het |
Fras1 |
C |
A |
5: 96,790,479 (GRCm39) |
T951K |
probably damaging |
Het |
Gen1 |
A |
T |
12: 11,292,363 (GRCm39) |
N475K |
possibly damaging |
Het |
Gm14569 |
T |
C |
X: 35,697,146 (GRCm39) |
Y521C |
probably benign |
Het |
Gm6124 |
T |
A |
7: 38,870,529 (GRCm39) |
|
noncoding transcript |
Het |
Gpt2 |
A |
T |
8: 86,252,188 (GRCm39) |
D501V |
probably benign |
Het |
Gstm2 |
T |
C |
3: 107,893,370 (GRCm39) |
K31R |
probably benign |
Het |
Homer3 |
G |
A |
8: 70,742,793 (GRCm39) |
|
probably null |
Het |
Itga1 |
T |
A |
13: 115,138,102 (GRCm39) |
M428L |
probably benign |
Het |
Kalrn |
C |
T |
16: 33,810,180 (GRCm39) |
D2525N |
possibly damaging |
Het |
Kcnn4 |
T |
C |
7: 24,076,867 (GRCm39) |
W139R |
probably benign |
Het |
Kdm7a |
T |
A |
6: 39,143,602 (GRCm39) |
R380W |
probably null |
Het |
Khdrbs1 |
T |
G |
4: 129,635,889 (GRCm39) |
D22A |
possibly damaging |
Het |
Liph |
A |
T |
16: 21,795,000 (GRCm39) |
I204N |
probably damaging |
Het |
Loxhd1 |
A |
G |
18: 77,529,456 (GRCm39) |
E2033G |
possibly damaging |
Het |
M6pr |
C |
T |
6: 122,291,982 (GRCm39) |
|
probably benign |
Het |
Mrm1 |
A |
G |
11: 84,709,915 (GRCm39) |
I95T |
probably damaging |
Het |
Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
Mug1 |
C |
A |
6: 121,856,311 (GRCm39) |
F1030L |
probably damaging |
Het |
Naca |
C |
T |
10: 127,879,341 (GRCm39) |
|
probably benign |
Het |
Nob1 |
A |
T |
8: 108,145,120 (GRCm39) |
|
probably benign |
Het |
Nutm1 |
A |
C |
2: 112,080,154 (GRCm39) |
I587R |
probably damaging |
Het |
Or1e26 |
A |
G |
11: 73,480,081 (GRCm39) |
V161A |
probably benign |
Het |
Pcdhb2 |
A |
G |
18: 37,428,455 (GRCm39) |
K143E |
probably benign |
Het |
Pcnt |
T |
C |
10: 76,228,227 (GRCm39) |
Q1646R |
probably benign |
Het |
Piwil2 |
A |
T |
14: 70,646,365 (GRCm39) |
D390E |
probably benign |
Het |
Pkhd1 |
A |
G |
1: 20,309,635 (GRCm39) |
L2771P |
probably damaging |
Het |
Pla2g1b |
T |
A |
5: 115,608,947 (GRCm39) |
Y47* |
probably null |
Het |
Plekhn1 |
T |
C |
4: 156,309,813 (GRCm39) |
T135A |
probably damaging |
Het |
Pola1 |
T |
C |
X: 92,605,029 (GRCm39) |
Y968C |
probably damaging |
Het |
Ppp1r26 |
C |
A |
2: 28,341,618 (GRCm39) |
T416K |
probably benign |
Het |
Psmd1 |
A |
G |
1: 86,003,673 (GRCm39) |
I153V |
possibly damaging |
Het |
Rcan2 |
A |
G |
17: 44,264,361 (GRCm39) |
D7G |
probably benign |
Het |
Rexo5 |
T |
C |
7: 119,433,599 (GRCm39) |
I326T |
possibly damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,530,802 (GRCm39) |
|
probably benign |
Het |
Shc1 |
T |
C |
3: 89,333,985 (GRCm39) |
S273P |
probably benign |
Het |
Slc9b2 |
T |
C |
3: 135,042,305 (GRCm39) |
V528A |
probably benign |
Het |
Tma16 |
C |
T |
8: 66,936,823 (GRCm39) |
|
probably null |
Het |
Tnfaip2 |
T |
C |
12: 111,416,285 (GRCm39) |
F516L |
probably benign |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Wdr35 |
A |
G |
12: 9,039,981 (GRCm39) |
D362G |
probably damaging |
Het |
Wwp2 |
T |
C |
8: 108,184,610 (GRCm39) |
V106A |
probably benign |
Het |
Zfp40 |
T |
A |
17: 23,395,693 (GRCm39) |
H230L |
possibly damaging |
Het |
Zkscan17 |
T |
A |
11: 59,393,848 (GRCm39) |
M1L |
possibly damaging |
Het |
|
Other mutations in Tas2r118 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01350:Tas2r118
|
APN |
6 |
23,969,746 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Tas2r118
|
APN |
6 |
23,969,891 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03387:Tas2r118
|
APN |
6 |
23,969,180 (GRCm39) |
missense |
possibly damaging |
0.71 |
PIT4382001:Tas2r118
|
UTSW |
6 |
23,969,785 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0241:Tas2r118
|
UTSW |
6 |
23,969,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Tas2r118
|
UTSW |
6 |
23,969,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0544:Tas2r118
|
UTSW |
6 |
23,969,400 (GRCm39) |
missense |
probably damaging |
0.97 |
R1438:Tas2r118
|
UTSW |
6 |
23,969,422 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1471:Tas2r118
|
UTSW |
6 |
23,969,170 (GRCm39) |
missense |
probably damaging |
0.96 |
R1632:Tas2r118
|
UTSW |
6 |
23,969,260 (GRCm39) |
missense |
probably benign |
0.21 |
R2096:Tas2r118
|
UTSW |
6 |
23,969,912 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2106:Tas2r118
|
UTSW |
6 |
23,969,569 (GRCm39) |
missense |
probably benign |
|
R2903:Tas2r118
|
UTSW |
6 |
23,969,801 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2904:Tas2r118
|
UTSW |
6 |
23,969,801 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2905:Tas2r118
|
UTSW |
6 |
23,969,801 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3798:Tas2r118
|
UTSW |
6 |
23,969,822 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4647:Tas2r118
|
UTSW |
6 |
23,969,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Tas2r118
|
UTSW |
6 |
23,969,225 (GRCm39) |
missense |
probably benign |
0.26 |
R4965:Tas2r118
|
UTSW |
6 |
23,969,627 (GRCm39) |
missense |
probably benign |
0.41 |
R5114:Tas2r118
|
UTSW |
6 |
23,969,209 (GRCm39) |
missense |
probably benign |
0.05 |
R5823:Tas2r118
|
UTSW |
6 |
23,969,470 (GRCm39) |
missense |
probably benign |
0.04 |
R5834:Tas2r118
|
UTSW |
6 |
23,969,876 (GRCm39) |
missense |
probably benign |
0.06 |
R6976:Tas2r118
|
UTSW |
6 |
23,969,470 (GRCm39) |
missense |
probably benign |
0.04 |
R7335:Tas2r118
|
UTSW |
6 |
23,969,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R8696:Tas2r118
|
UTSW |
6 |
23,969,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Tas2r118
|
UTSW |
6 |
23,970,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R9014:Tas2r118
|
UTSW |
6 |
23,970,049 (GRCm39) |
missense |
probably benign |
0.04 |
R9237:Tas2r118
|
UTSW |
6 |
23,969,617 (GRCm39) |
missense |
probably benign |
0.09 |
X0062:Tas2r118
|
UTSW |
6 |
23,969,439 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tas2r118
|
UTSW |
6 |
23,969,558 (GRCm39) |
missense |
probably benign |
|
|