Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd12 |
A |
T |
2: 150,677,226 (GRCm39) |
*56R |
probably null |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Arfgap3 |
C |
T |
15: 83,216,898 (GRCm39) |
A156T |
probably benign |
Het |
Bpifc |
T |
C |
10: 85,836,497 (GRCm39) |
T3A |
probably benign |
Het |
Ccdc7a |
T |
A |
8: 129,715,278 (GRCm39) |
I269L |
probably benign |
Het |
Cd151 |
A |
G |
7: 141,050,606 (GRCm39) |
Y253C |
probably damaging |
Het |
Cenpl |
C |
A |
1: 160,911,037 (GRCm39) |
S328* |
probably null |
Het |
Cfl1 |
T |
A |
19: 5,542,580 (GRCm39) |
V20D |
probably damaging |
Het |
Clec14a |
A |
G |
12: 58,315,400 (GRCm39) |
L74P |
probably damaging |
Het |
Cnn1 |
A |
T |
9: 22,019,132 (GRCm39) |
D196V |
probably damaging |
Het |
Cst13 |
C |
A |
2: 148,670,143 (GRCm39) |
C104* |
probably null |
Het |
Det1 |
A |
G |
7: 78,493,302 (GRCm39) |
V234A |
probably damaging |
Het |
Efnb2 |
A |
G |
8: 8,673,162 (GRCm39) |
M165T |
probably damaging |
Het |
Fbxo10 |
T |
A |
4: 45,051,573 (GRCm39) |
K339* |
probably null |
Het |
Fnta |
A |
T |
8: 26,501,246 (GRCm39) |
|
probably null |
Het |
Fsip2 |
A |
T |
2: 82,813,338 (GRCm39) |
Y3219F |
possibly damaging |
Het |
Gprin2 |
C |
T |
14: 33,916,832 (GRCm39) |
V313M |
possibly damaging |
Het |
Hars1 |
A |
G |
18: 36,900,358 (GRCm39) |
L448S |
possibly damaging |
Het |
Hipk3 |
A |
G |
2: 104,260,345 (GRCm39) |
I1166T |
possibly damaging |
Het |
Il31ra |
T |
C |
13: 112,660,864 (GRCm39) |
E602G |
probably benign |
Het |
Kctd15 |
A |
G |
7: 34,344,282 (GRCm39) |
L123P |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,395,175 (GRCm39) |
D489G |
possibly damaging |
Het |
Krt1 |
C |
A |
15: 101,754,357 (GRCm39) |
S631I |
unknown |
Het |
Lancl1 |
T |
A |
1: 67,060,173 (GRCm39) |
Y84F |
probably benign |
Het |
Lcor |
A |
G |
19: 41,570,969 (GRCm39) |
D54G |
probably damaging |
Het |
Mafa |
G |
T |
15: 75,619,666 (GRCm39) |
P36T |
unknown |
Het |
Magi2 |
G |
A |
5: 20,563,970 (GRCm39) |
|
probably null |
Het |
Mcm9 |
T |
A |
10: 53,492,134 (GRCm39) |
I396F |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,942 (GRCm39) |
F61L |
probably damaging |
Het |
Or10g1b |
A |
G |
14: 52,628,069 (GRCm39) |
W54R |
probably benign |
Het |
Or1e16 |
TAGCGGTCGTA |
T |
11: 73,286,479 (GRCm39) |
|
probably null |
Het |
Or1e16 |
AGCGGTCGTAGGC |
AGC |
11: 73,286,480 (GRCm39) |
|
probably null |
Het |
Or51a7 |
T |
A |
7: 102,615,143 (GRCm39) |
F279I |
possibly damaging |
Het |
Or5w17 |
A |
T |
2: 87,583,448 (GRCm39) |
D296E |
possibly damaging |
Het |
Pcsk5 |
T |
A |
19: 17,542,174 (GRCm39) |
T806S |
possibly damaging |
Het |
Pigc |
T |
C |
1: 161,798,465 (GRCm39) |
I149T |
possibly damaging |
Het |
Pou5f2 |
C |
A |
13: 78,173,083 (GRCm39) |
N8K |
probably benign |
Het |
Pou6f2 |
T |
C |
13: 18,300,129 (GRCm39) |
|
probably benign |
Het |
Prl3d2 |
T |
A |
13: 27,306,312 (GRCm39) |
M13K |
possibly damaging |
Het |
Pzp |
T |
C |
6: 128,479,297 (GRCm39) |
N619D |
probably benign |
Het |
Rnps1 |
G |
A |
17: 24,637,517 (GRCm39) |
S53N |
probably benign |
Het |
Scaf8 |
C |
G |
17: 3,240,440 (GRCm39) |
A604G |
probably benign |
Het |
Scn10a |
T |
C |
9: 119,438,721 (GRCm39) |
N1716S |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc34a1 |
A |
G |
13: 24,003,845 (GRCm39) |
|
probably null |
Het |
Syne2 |
A |
G |
12: 76,141,194 (GRCm39) |
D6102G |
probably damaging |
Het |
Tbc1d16 |
A |
T |
11: 119,049,646 (GRCm39) |
D283E |
probably benign |
Het |
Tet1 |
T |
C |
10: 62,674,026 (GRCm39) |
D1350G |
probably benign |
Het |
Tyro3 |
T |
C |
2: 119,640,998 (GRCm39) |
L494P |
probably damaging |
Het |
Uba6 |
G |
T |
5: 86,272,281 (GRCm39) |
Q803K |
probably benign |
Het |
Vgll2 |
T |
A |
10: 51,904,088 (GRCm39) |
L317Q |
possibly damaging |
Het |
Wdr62 |
A |
T |
7: 29,964,592 (GRCm39) |
I384N |
probably damaging |
Het |
Wdtc1 |
G |
A |
4: 133,021,678 (GRCm39) |
R619* |
probably null |
Het |
Xkr6 |
A |
G |
14: 64,056,356 (GRCm39) |
D89G |
possibly damaging |
Het |
|
Other mutations in Trpa1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00801:Trpa1
|
APN |
1 |
14,961,557 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00937:Trpa1
|
APN |
1 |
14,950,501 (GRCm39) |
splice site |
probably benign |
|
IGL00957:Trpa1
|
APN |
1 |
14,951,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01307:Trpa1
|
APN |
1 |
14,966,771 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01336:Trpa1
|
APN |
1 |
14,957,104 (GRCm39) |
splice site |
probably benign |
|
IGL01408:Trpa1
|
APN |
1 |
14,959,637 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01504:Trpa1
|
APN |
1 |
14,952,443 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01543:Trpa1
|
APN |
1 |
14,970,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01609:Trpa1
|
APN |
1 |
14,982,607 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01895:Trpa1
|
APN |
1 |
14,957,867 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02449:Trpa1
|
APN |
1 |
14,968,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02936:Trpa1
|
APN |
1 |
14,946,193 (GRCm39) |
splice site |
probably null |
|
fear-2
|
UTSW |
1 |
14,961,527 (GRCm39) |
critical splice donor site |
probably null |
|
petrified
|
UTSW |
1 |
14,954,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Trpa1
|
UTSW |
1 |
14,973,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0008:Trpa1
|
UTSW |
1 |
14,973,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0317:Trpa1
|
UTSW |
1 |
14,951,856 (GRCm39) |
missense |
probably benign |
0.03 |
R0454:Trpa1
|
UTSW |
1 |
14,955,972 (GRCm39) |
critical splice donor site |
probably null |
|
R0828:Trpa1
|
UTSW |
1 |
14,946,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R0944:Trpa1
|
UTSW |
1 |
14,982,585 (GRCm39) |
splice site |
probably null |
|
R0962:Trpa1
|
UTSW |
1 |
14,968,387 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1025:Trpa1
|
UTSW |
1 |
14,974,407 (GRCm39) |
missense |
probably benign |
0.01 |
R1035:Trpa1
|
UTSW |
1 |
14,961,527 (GRCm39) |
critical splice donor site |
probably null |
|
R1134:Trpa1
|
UTSW |
1 |
14,951,972 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1278:Trpa1
|
UTSW |
1 |
14,988,947 (GRCm39) |
critical splice donor site |
probably null |
|
R1497:Trpa1
|
UTSW |
1 |
14,956,036 (GRCm39) |
missense |
probably benign |
0.30 |
R1617:Trpa1
|
UTSW |
1 |
14,943,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1800:Trpa1
|
UTSW |
1 |
14,944,648 (GRCm39) |
missense |
probably benign |
0.04 |
R1856:Trpa1
|
UTSW |
1 |
14,969,612 (GRCm39) |
nonsense |
probably null |
|
R1886:Trpa1
|
UTSW |
1 |
14,959,649 (GRCm39) |
missense |
probably benign |
0.00 |
R2004:Trpa1
|
UTSW |
1 |
14,976,207 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2152:Trpa1
|
UTSW |
1 |
14,969,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Trpa1
|
UTSW |
1 |
14,951,880 (GRCm39) |
missense |
probably benign |
0.01 |
R2198:Trpa1
|
UTSW |
1 |
14,980,970 (GRCm39) |
missense |
probably benign |
|
R2221:Trpa1
|
UTSW |
1 |
14,973,480 (GRCm39) |
missense |
probably null |
0.12 |
R2223:Trpa1
|
UTSW |
1 |
14,973,480 (GRCm39) |
missense |
probably null |
0.12 |
R2307:Trpa1
|
UTSW |
1 |
14,982,605 (GRCm39) |
missense |
probably benign |
0.00 |
R2338:Trpa1
|
UTSW |
1 |
14,954,469 (GRCm39) |
missense |
probably damaging |
0.97 |
R2698:Trpa1
|
UTSW |
1 |
14,976,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Trpa1
|
UTSW |
1 |
14,957,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Trpa1
|
UTSW |
1 |
14,957,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R2873:Trpa1
|
UTSW |
1 |
14,957,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R2874:Trpa1
|
UTSW |
1 |
14,957,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Trpa1
|
UTSW |
1 |
14,944,605 (GRCm39) |
missense |
probably benign |
0.01 |
R3419:Trpa1
|
UTSW |
1 |
14,944,605 (GRCm39) |
missense |
probably benign |
0.01 |
R3796:Trpa1
|
UTSW |
1 |
14,963,488 (GRCm39) |
missense |
possibly damaging |
0.74 |
R3799:Trpa1
|
UTSW |
1 |
14,963,488 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4238:Trpa1
|
UTSW |
1 |
14,954,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R4320:Trpa1
|
UTSW |
1 |
14,944,676 (GRCm39) |
missense |
probably benign |
0.00 |
R4591:Trpa1
|
UTSW |
1 |
14,952,332 (GRCm39) |
splice site |
probably null |
|
R4834:Trpa1
|
UTSW |
1 |
14,966,747 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4991:Trpa1
|
UTSW |
1 |
14,980,970 (GRCm39) |
missense |
probably benign |
0.00 |
R4999:Trpa1
|
UTSW |
1 |
14,946,085 (GRCm39) |
missense |
probably benign |
0.05 |
R5038:Trpa1
|
UTSW |
1 |
14,981,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5055:Trpa1
|
UTSW |
1 |
14,946,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Trpa1
|
UTSW |
1 |
14,951,885 (GRCm39) |
missense |
probably benign |
0.01 |
R5558:Trpa1
|
UTSW |
1 |
14,968,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5578:Trpa1
|
UTSW |
1 |
14,957,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R5680:Trpa1
|
UTSW |
1 |
14,946,078 (GRCm39) |
missense |
probably benign |
0.00 |
R5738:Trpa1
|
UTSW |
1 |
14,946,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R5801:Trpa1
|
UTSW |
1 |
14,968,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5945:Trpa1
|
UTSW |
1 |
14,968,359 (GRCm39) |
missense |
probably benign |
0.03 |
R6092:Trpa1
|
UTSW |
1 |
14,959,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Trpa1
|
UTSW |
1 |
14,982,601 (GRCm39) |
missense |
probably benign |
|
R7126:Trpa1
|
UTSW |
1 |
14,960,648 (GRCm39) |
missense |
probably benign |
0.00 |
R7154:Trpa1
|
UTSW |
1 |
14,952,457 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7175:Trpa1
|
UTSW |
1 |
14,963,431 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7258:Trpa1
|
UTSW |
1 |
14,973,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Trpa1
|
UTSW |
1 |
14,968,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Trpa1
|
UTSW |
1 |
14,954,422 (GRCm39) |
missense |
probably benign |
0.43 |
R7639:Trpa1
|
UTSW |
1 |
14,957,137 (GRCm39) |
missense |
probably benign |
0.00 |
R7740:Trpa1
|
UTSW |
1 |
14,982,625 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7815:Trpa1
|
UTSW |
1 |
14,974,486 (GRCm39) |
missense |
probably benign |
0.01 |
R7854:Trpa1
|
UTSW |
1 |
14,951,918 (GRCm39) |
missense |
probably benign |
0.00 |
R8112:Trpa1
|
UTSW |
1 |
14,974,490 (GRCm39) |
missense |
probably benign |
|
R8217:Trpa1
|
UTSW |
1 |
14,957,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R8711:Trpa1
|
UTSW |
1 |
14,980,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R8834:Trpa1
|
UTSW |
1 |
14,963,528 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8907:Trpa1
|
UTSW |
1 |
14,963,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Trpa1
|
UTSW |
1 |
14,959,664 (GRCm39) |
missense |
probably benign |
0.00 |
R9058:Trpa1
|
UTSW |
1 |
14,959,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R9135:Trpa1
|
UTSW |
1 |
14,952,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Trpa1
|
UTSW |
1 |
14,963,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R9266:Trpa1
|
UTSW |
1 |
14,980,953 (GRCm39) |
critical splice donor site |
probably null |
|
R9287:Trpa1
|
UTSW |
1 |
14,956,040 (GRCm39) |
nonsense |
probably null |
|
R9323:Trpa1
|
UTSW |
1 |
14,968,564 (GRCm39) |
missense |
probably benign |
0.01 |
R9379:Trpa1
|
UTSW |
1 |
14,966,739 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9497:Trpa1
|
UTSW |
1 |
14,989,026 (GRCm39) |
missense |
probably benign |
0.02 |
R9616:Trpa1
|
UTSW |
1 |
14,989,077 (GRCm39) |
start gained |
probably benign |
|
R9666:Trpa1
|
UTSW |
1 |
14,973,455 (GRCm39) |
missense |
possibly damaging |
0.67 |
X0028:Trpa1
|
UTSW |
1 |
14,960,644 (GRCm39) |
missense |
probably benign |
0.16 |
Z1176:Trpa1
|
UTSW |
1 |
14,968,574 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Trpa1
|
UTSW |
1 |
14,961,530 (GRCm39) |
missense |
possibly damaging |
0.80 |
Z1176:Trpa1
|
UTSW |
1 |
14,951,916 (GRCm39) |
missense |
probably damaging |
1.00 |
|