Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730522E02Rik |
C |
T |
11: 25,602,020 (GRCm39) |
C70Y |
unknown |
Het |
Abi3bp |
C |
T |
16: 56,498,193 (GRCm39) |
T929I |
probably damaging |
Het |
Adap2 |
C |
A |
11: 80,056,490 (GRCm39) |
|
probably benign |
Het |
Adgrg5 |
A |
G |
8: 95,668,413 (GRCm39) |
|
probably null |
Het |
Afdn |
C |
A |
17: 14,124,260 (GRCm39) |
N1803K |
probably damaging |
Het |
Alox12b |
T |
C |
11: 69,057,132 (GRCm39) |
L451P |
possibly damaging |
Het |
Ankrd26 |
T |
C |
6: 118,510,434 (GRCm39) |
|
probably benign |
Het |
Bcr |
A |
T |
10: 74,993,039 (GRCm39) |
|
probably benign |
Het |
Cacna1c |
T |
C |
6: 118,734,347 (GRCm39) |
N300D |
probably benign |
Het |
Camsap1 |
G |
T |
2: 25,829,097 (GRCm39) |
Q876K |
probably damaging |
Het |
Cdh10 |
A |
G |
15: 18,986,837 (GRCm39) |
D356G |
possibly damaging |
Het |
Cdipt |
T |
A |
7: 126,576,092 (GRCm39) |
Y16N |
probably damaging |
Het |
Cebpz |
T |
C |
17: 79,233,411 (GRCm39) |
E772G |
probably benign |
Het |
Cep350 |
A |
G |
1: 155,828,992 (GRCm39) |
I304T |
probably benign |
Het |
Chpt1 |
C |
A |
10: 88,312,277 (GRCm39) |
G9V |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,739,263 (GRCm39) |
|
probably null |
Het |
Dock7 |
G |
T |
4: 98,903,982 (GRCm39) |
P688T |
probably damaging |
Het |
Ephb3 |
T |
A |
16: 21,037,784 (GRCm39) |
|
probably benign |
Het |
Fcgr2b |
T |
C |
1: 170,788,599 (GRCm39) |
Y336C |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,110,639 (GRCm39) |
H889L |
unknown |
Het |
Gucy2c |
C |
T |
6: 136,686,746 (GRCm39) |
V806M |
probably damaging |
Het |
Hmgxb3 |
T |
A |
18: 61,304,426 (GRCm39) |
I55F |
probably damaging |
Het |
Igsf9b |
T |
A |
9: 27,230,901 (GRCm39) |
Y301* |
probably null |
Het |
Il12rb2 |
C |
T |
6: 67,333,691 (GRCm39) |
R196H |
probably benign |
Het |
Itgam |
T |
C |
7: 127,715,677 (GRCm39) |
|
probably null |
Het |
Klhl25 |
T |
C |
7: 75,515,943 (GRCm39) |
V283A |
probably damaging |
Het |
Klhl5 |
T |
C |
5: 65,320,135 (GRCm39) |
L423P |
probably damaging |
Het |
Krt6a |
T |
C |
15: 101,602,271 (GRCm39) |
N138S |
probably damaging |
Het |
Lrba |
A |
T |
3: 86,515,677 (GRCm39) |
|
probably null |
Het |
Map4k5 |
T |
C |
12: 69,852,100 (GRCm39) |
T828A |
probably damaging |
Het |
Marchf8 |
T |
A |
6: 116,382,639 (GRCm39) |
M434K |
probably benign |
Het |
Mink1 |
C |
T |
11: 70,500,971 (GRCm39) |
Q743* |
probably null |
Het |
Mrgpra3 |
T |
C |
7: 47,239,884 (GRCm39) |
N14S |
probably benign |
Het |
Mroh7 |
T |
C |
4: 106,557,073 (GRCm39) |
S808G |
probably damaging |
Het |
Msi1 |
T |
C |
5: 115,568,953 (GRCm39) |
|
probably null |
Het |
Nrap |
A |
G |
19: 56,333,990 (GRCm39) |
Y874H |
probably damaging |
Het |
Nup205 |
T |
C |
6: 35,171,501 (GRCm39) |
F455L |
probably benign |
Het |
Or2t1 |
G |
T |
14: 14,328,800 (GRCm38) |
V230L |
probably benign |
Het |
Piwil2 |
A |
G |
14: 70,613,466 (GRCm39) |
V894A |
probably damaging |
Het |
Polr1c |
A |
G |
17: 46,555,990 (GRCm39) |
S173P |
probably damaging |
Het |
Pphln1-ps1 |
A |
G |
16: 13,495,669 (GRCm39) |
Y256C |
probably damaging |
Het |
Prep |
C |
T |
10: 45,031,621 (GRCm39) |
A564V |
probably benign |
Het |
Rab3gap1 |
T |
C |
1: 127,865,922 (GRCm39) |
|
probably benign |
Het |
Rcc1 |
G |
C |
4: 132,063,136 (GRCm39) |
|
probably benign |
Het |
Scn11a |
T |
A |
9: 119,584,073 (GRCm39) |
D1514V |
probably benign |
Het |
Setdb1 |
G |
A |
3: 95,246,171 (GRCm39) |
P584S |
probably damaging |
Het |
Slc12a7 |
A |
G |
13: 73,936,771 (GRCm39) |
I144V |
probably benign |
Het |
Slc45a4 |
T |
C |
15: 73,458,665 (GRCm39) |
M295V |
probably benign |
Het |
Slco1a1 |
T |
A |
6: 141,867,565 (GRCm39) |
D456V |
possibly damaging |
Het |
Sspo |
G |
T |
6: 48,475,668 (GRCm39) |
C4928F |
probably damaging |
Het |
St6galnac1 |
T |
A |
11: 116,659,823 (GRCm39) |
K163N |
probably benign |
Het |
Tcp11l1 |
A |
T |
2: 104,530,181 (GRCm39) |
|
probably benign |
Het |
Tns1 |
T |
A |
1: 73,958,825 (GRCm39) |
I1715F |
probably damaging |
Het |
Ttc28 |
A |
G |
5: 111,371,312 (GRCm39) |
E587G |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,177,864 (GRCm39) |
|
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm39) |
P46S |
probably benign |
Het |
Usp8 |
G |
A |
2: 126,584,034 (GRCm39) |
|
probably benign |
Het |
Zfc3h1 |
G |
T |
10: 115,237,612 (GRCm39) |
A464S |
possibly damaging |
Het |
Zfp106 |
T |
C |
2: 120,366,084 (GRCm39) |
I108V |
probably benign |
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 |
|
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 |
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 |
|