Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
G |
A |
5: 109,885,370 (GRCm39) |
Q163* |
probably null |
Het |
Anxa6 |
T |
A |
11: 54,898,725 (GRCm39) |
T150S |
probably damaging |
Het |
Bpifb6 |
T |
A |
2: 153,744,929 (GRCm39) |
L45Q |
probably damaging |
Het |
Brwd1 |
T |
C |
16: 95,828,568 (GRCm39) |
D1121G |
probably damaging |
Het |
C1ql3 |
A |
G |
2: 13,015,483 (GRCm39) |
I59T |
possibly damaging |
Het |
Ccdc80 |
A |
G |
16: 44,924,888 (GRCm39) |
H674R |
possibly damaging |
Het |
Cdhr1 |
T |
G |
14: 36,811,337 (GRCm39) |
E258A |
probably damaging |
Het |
Ces2g |
T |
A |
8: 105,692,962 (GRCm39) |
F333L |
probably damaging |
Het |
Chn2 |
C |
T |
6: 54,277,156 (GRCm39) |
T445I |
probably benign |
Het |
Cpe |
T |
C |
8: 65,050,562 (GRCm39) |
D382G |
possibly damaging |
Het |
Crb1 |
T |
A |
1: 139,165,428 (GRCm39) |
I960L |
probably benign |
Het |
Cyp4a14 |
A |
T |
4: 115,350,806 (GRCm39) |
V156D |
probably damaging |
Het |
Ddx23 |
A |
T |
15: 98,556,315 (GRCm39) |
M1K |
probably null |
Het |
Dnajc7 |
T |
C |
11: 100,482,387 (GRCm39) |
I202V |
probably benign |
Het |
Dsn1 |
T |
A |
2: 156,839,636 (GRCm39) |
D255V |
possibly damaging |
Het |
Dvl3 |
A |
T |
16: 20,346,000 (GRCm39) |
|
probably null |
Het |
Epm2a |
A |
G |
10: 11,266,684 (GRCm39) |
D143G |
possibly damaging |
Het |
Erc1 |
T |
A |
6: 119,738,149 (GRCm39) |
M565L |
probably benign |
Het |
Fancm |
T |
C |
12: 65,173,321 (GRCm39) |
C1878R |
possibly damaging |
Het |
Gapvd1 |
T |
C |
2: 34,590,834 (GRCm39) |
E946G |
probably damaging |
Het |
Gm9195 |
C |
T |
14: 72,678,113 (GRCm39) |
R2352K |
possibly damaging |
Het |
Greb1 |
C |
A |
12: 16,790,122 (GRCm39) |
|
probably benign |
Het |
Haus5 |
G |
A |
7: 30,362,678 (GRCm39) |
A44V |
possibly damaging |
Het |
Herc4 |
A |
G |
10: 63,105,457 (GRCm39) |
Y146C |
probably benign |
Het |
Herc6 |
T |
G |
6: 57,636,802 (GRCm39) |
|
probably null |
Het |
Hivep2 |
G |
T |
10: 14,003,414 (GRCm39) |
G4V |
probably damaging |
Het |
Hsdl2 |
G |
T |
4: 59,612,724 (GRCm39) |
G425V |
probably damaging |
Het |
Igkv1-110 |
C |
T |
6: 68,247,974 (GRCm39) |
L28F |
probably benign |
Het |
Il21r |
T |
A |
7: 125,231,727 (GRCm39) |
L385Q |
possibly damaging |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Krtap5-2 |
C |
T |
7: 141,728,699 (GRCm39) |
C149Y |
unknown |
Het |
Lingo2 |
T |
A |
4: 35,709,248 (GRCm39) |
N244I |
probably damaging |
Het |
Lrrk2 |
C |
T |
15: 91,651,527 (GRCm39) |
R1728C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,578,096 (GRCm39) |
|
probably benign |
Het |
Malrd1 |
G |
A |
2: 15,619,026 (GRCm39) |
V297I |
not run |
Het |
Mars1 |
T |
A |
10: 127,136,444 (GRCm39) |
E460D |
probably benign |
Het |
Nr1i3 |
A |
G |
1: 171,044,396 (GRCm39) |
I174V |
probably benign |
Het |
Odf2 |
C |
T |
2: 29,820,636 (GRCm39) |
T814M |
probably damaging |
Het |
Or10q1 |
T |
C |
19: 13,727,328 (GRCm39) |
V286A |
probably benign |
Het |
Or4k1 |
T |
C |
14: 50,377,803 (GRCm39) |
M98V |
probably benign |
Het |
Or4k52 |
A |
T |
2: 111,610,793 (GRCm39) |
I43F |
possibly damaging |
Het |
Pcdhga8 |
T |
C |
18: 37,860,470 (GRCm39) |
S509P |
probably benign |
Het |
Pdzd2 |
A |
G |
15: 12,374,102 (GRCm39) |
L2011S |
probably benign |
Het |
Pole |
T |
A |
5: 110,478,907 (GRCm39) |
S1930T |
probably benign |
Het |
Poteg |
T |
A |
8: 27,952,052 (GRCm39) |
|
probably null |
Het |
Ptprk |
T |
A |
10: 28,372,920 (GRCm39) |
C724S |
probably damaging |
Het |
Rabgap1l |
T |
C |
1: 160,509,673 (GRCm39) |
E468G |
probably benign |
Het |
Rbm12b1 |
G |
T |
4: 12,145,954 (GRCm39) |
R642L |
probably benign |
Het |
Relch |
T |
C |
1: 105,658,986 (GRCm39) |
V914A |
probably damaging |
Het |
S1pr4 |
A |
T |
10: 81,334,855 (GRCm39) |
Y206* |
probably null |
Het |
Sim2 |
A |
G |
16: 93,915,819 (GRCm39) |
I261V |
probably benign |
Het |
Slc22a12 |
C |
A |
19: 6,587,199 (GRCm39) |
A448S |
probably benign |
Het |
Slc4a2 |
A |
G |
5: 24,636,666 (GRCm39) |
|
probably null |
Het |
Slc6a7 |
T |
C |
18: 61,133,495 (GRCm39) |
E567G |
possibly damaging |
Het |
St6gal1 |
T |
C |
16: 23,139,785 (GRCm39) |
|
probably benign |
Het |
Syne3 |
T |
C |
12: 104,920,546 (GRCm39) |
K550R |
probably benign |
Het |
Tekt1 |
T |
A |
11: 72,250,544 (GRCm39) |
T51S |
probably benign |
Het |
Tm9sf4 |
T |
A |
2: 153,050,663 (GRCm39) |
V640E |
probably damaging |
Het |
Tnfsf8 |
G |
T |
4: 63,752,683 (GRCm39) |
H127Q |
possibly damaging |
Het |
Tomm20 |
A |
G |
8: 127,666,633 (GRCm39) |
L80S |
probably damaging |
Het |
Top2a |
T |
C |
11: 98,884,640 (GRCm39) |
D1526G |
probably benign |
Het |
Trmt1l |
T |
C |
1: 151,316,639 (GRCm39) |
V200A |
possibly damaging |
Het |
Vmn2r12 |
A |
T |
5: 109,239,615 (GRCm39) |
V316D |
probably damaging |
Het |
Vmn2r14 |
A |
T |
5: 109,368,324 (GRCm39) |
L223M |
probably benign |
Het |
Zfp2 |
T |
C |
11: 50,791,605 (GRCm39) |
H146R |
probably damaging |
Het |
Zfp52 |
T |
C |
17: 21,781,252 (GRCm39) |
S367P |
probably 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 |
R5193:Trpa1
|
UTSW |
1 |
14,946,141 (GRCm39) |
missense |
possibly damaging |
0.92 |
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 |
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 |
|