Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap4e1 |
T |
A |
2: 126,889,061 (GRCm39) |
F509I |
probably damaging |
Het |
Asmt |
A |
T |
X: 169,106,456 (GRCm39) |
M19L |
probably benign |
Het |
Atf6 |
C |
T |
1: 170,621,608 (GRCm39) |
R471Q |
probably damaging |
Het |
Atp4a |
G |
A |
7: 30,419,650 (GRCm39) |
R671Q |
probably benign |
Het |
Baiap3 |
T |
A |
17: 25,468,510 (GRCm39) |
D250V |
probably damaging |
Het |
C2cd4d |
T |
A |
3: 94,271,054 (GRCm39) |
F107I |
probably damaging |
Het |
Cdkn2d |
C |
G |
9: 21,202,185 (GRCm39) |
V21L |
probably benign |
Het |
Cldn6 |
T |
C |
17: 23,900,060 (GRCm39) |
|
probably null |
Het |
Cpa5 |
A |
G |
6: 30,626,323 (GRCm39) |
N228S |
possibly damaging |
Het |
Cracdl |
T |
C |
1: 37,663,834 (GRCm39) |
E163G |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,747,716 (GRCm39) |
S1478G |
possibly damaging |
Het |
Csmd1 |
A |
T |
8: 15,995,011 (GRCm39) |
C2675S |
probably damaging |
Het |
Cthrc1 |
C |
A |
15: 38,940,408 (GRCm39) |
Q4K |
probably benign |
Het |
Ddo |
A |
T |
10: 40,523,543 (GRCm39) |
I178F |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,026,399 (GRCm39) |
T1836A |
probably benign |
Het |
Dnah9 |
T |
G |
11: 66,038,215 (GRCm39) |
Q107P |
probably damaging |
Het |
Dusp26 |
A |
G |
8: 31,584,172 (GRCm39) |
N93S |
probably damaging |
Het |
Egr2 |
GAA |
GA |
10: 67,375,733 (GRCm39) |
|
probably null |
Het |
Epha5 |
T |
C |
5: 84,304,303 (GRCm39) |
I501V |
probably damaging |
Het |
Eya1 |
C |
T |
1: 14,253,420 (GRCm39) |
V519M |
probably damaging |
Het |
Fam227b |
T |
A |
2: 125,988,188 (GRCm39) |
|
probably benign |
Het |
Fgd5 |
C |
T |
6: 91,966,167 (GRCm39) |
S642F |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,821,120 (GRCm39) |
A5618S |
possibly damaging |
Het |
Gm12034 |
T |
A |
11: 20,396,476 (GRCm39) |
|
noncoding transcript |
Het |
Liph |
T |
C |
16: 21,803,018 (GRCm39) |
D17G |
probably benign |
Het |
Mbd3 |
A |
T |
10: 80,229,817 (GRCm39) |
L164H |
probably damaging |
Het |
Med4 |
A |
G |
14: 73,755,502 (GRCm39) |
|
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Or4k1 |
T |
C |
14: 50,377,953 (GRCm39) |
I48V |
probably benign |
Het |
Or8b1b |
C |
A |
9: 38,375,938 (GRCm39) |
F200L |
probably benign |
Het |
Pcdha11 |
G |
A |
18: 37,140,426 (GRCm39) |
G685D |
probably benign |
Het |
Pgc |
A |
G |
17: 48,043,335 (GRCm39) |
I228V |
probably benign |
Het |
Pramel25 |
A |
G |
4: 143,519,394 (GRCm39) |
S52G |
probably benign |
Het |
Rad51 |
C |
T |
2: 118,962,049 (GRCm39) |
H199Y |
probably damaging |
Het |
Robo2 |
A |
T |
16: 74,149,407 (GRCm39) |
|
probably benign |
Het |
Sap130 |
C |
T |
18: 31,844,413 (GRCm39) |
T861I |
probably damaging |
Het |
Sh3tc2 |
A |
T |
18: 62,140,844 (GRCm39) |
D1061V |
probably damaging |
Het |
Shoc1 |
T |
C |
4: 59,092,383 (GRCm39) |
D266G |
possibly damaging |
Het |
Snapc3 |
A |
G |
4: 83,336,996 (GRCm39) |
E119G |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,464,159 (GRCm39) |
G3862D |
probably benign |
Het |
Tbc1d16 |
G |
A |
11: 119,048,699 (GRCm39) |
T318M |
possibly damaging |
Het |
Thrb |
T |
A |
14: 18,011,187 (GRCm38) |
W188R |
probably damaging |
Het |
Thsd1 |
T |
C |
8: 22,733,594 (GRCm39) |
Y214H |
probably damaging |
Het |
Tnfrsf13b |
T |
C |
11: 61,032,264 (GRCm39) |
V98A |
probably benign |
Het |
Topbp1 |
T |
C |
9: 103,222,070 (GRCm39) |
Y1314H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,616,150 (GRCm39) |
V8271L |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,777,257 (GRCm39) |
M1382V |
probably benign |
Het |
Utrn |
G |
T |
10: 12,603,584 (GRCm39) |
Q599K |
possibly damaging |
Het |
Zfp995 |
G |
A |
17: 22,098,932 (GRCm39) |
T434I |
probably benign |
Het |
Zfy1 |
G |
T |
Y: 725,518 (GRCm39) |
T749K |
possibly damaging |
Het |
|
Other mutations in Nav2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01097:Nav2
|
APN |
7 |
49,220,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01150:Nav2
|
APN |
7 |
49,102,269 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01649:Nav2
|
APN |
7 |
49,225,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Nav2
|
APN |
7 |
49,220,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02297:Nav2
|
APN |
7 |
49,243,977 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02313:Nav2
|
APN |
7 |
49,208,521 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02441:Nav2
|
APN |
7 |
49,102,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:Nav2
|
APN |
7 |
49,195,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02477:Nav2
|
APN |
7 |
49,232,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02725:Nav2
|
APN |
7 |
49,214,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02944:Nav2
|
APN |
7 |
49,070,004 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02953:Nav2
|
APN |
7 |
49,198,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Nav2
|
APN |
7 |
49,114,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Nav2
|
APN |
7 |
49,111,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03274:Nav2
|
APN |
7 |
49,011,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Nav2
|
APN |
7 |
49,141,205 (GRCm39) |
nonsense |
probably null |
|
R0006:Nav2
|
UTSW |
7 |
49,102,978 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0070:Nav2
|
UTSW |
7 |
49,220,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Nav2
|
UTSW |
7 |
49,185,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Nav2
|
UTSW |
7 |
49,195,651 (GRCm39) |
missense |
probably benign |
0.01 |
R0346:Nav2
|
UTSW |
7 |
49,254,333 (GRCm39) |
missense |
probably benign |
0.11 |
R0539:Nav2
|
UTSW |
7 |
49,111,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Nav2
|
UTSW |
7 |
49,058,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Nav2
|
UTSW |
7 |
49,070,081 (GRCm39) |
missense |
probably benign |
0.06 |
R0970:Nav2
|
UTSW |
7 |
49,233,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Nav2
|
UTSW |
7 |
49,185,788 (GRCm39) |
splice site |
probably benign |
|
R1274:Nav2
|
UTSW |
7 |
49,254,178 (GRCm39) |
nonsense |
probably null |
|
R1463:Nav2
|
UTSW |
7 |
49,185,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Nav2
|
UTSW |
7 |
49,011,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Nav2
|
UTSW |
7 |
49,011,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1536:Nav2
|
UTSW |
7 |
49,195,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Nav2
|
UTSW |
7 |
49,220,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Nav2
|
UTSW |
7 |
49,102,213 (GRCm39) |
missense |
probably benign |
|
R1731:Nav2
|
UTSW |
7 |
49,197,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Nav2
|
UTSW |
7 |
49,225,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Nav2
|
UTSW |
7 |
49,197,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1945:Nav2
|
UTSW |
7 |
49,114,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Nav2
|
UTSW |
7 |
49,198,219 (GRCm39) |
missense |
probably benign |
0.16 |
R2061:Nav2
|
UTSW |
7 |
49,248,645 (GRCm39) |
splice site |
probably benign |
|
R2117:Nav2
|
UTSW |
7 |
49,114,328 (GRCm39) |
missense |
probably benign |
0.00 |
R2174:Nav2
|
UTSW |
7 |
49,102,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R2182:Nav2
|
UTSW |
7 |
49,247,002 (GRCm39) |
missense |
probably benign |
0.38 |
R2251:Nav2
|
UTSW |
7 |
49,103,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R2283:Nav2
|
UTSW |
7 |
49,141,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Nav2
|
UTSW |
7 |
49,248,565 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2472:Nav2
|
UTSW |
7 |
49,058,632 (GRCm39) |
missense |
probably benign |
|
R2568:Nav2
|
UTSW |
7 |
49,247,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Nav2
|
UTSW |
7 |
49,195,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2964:Nav2
|
UTSW |
7 |
49,206,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Nav2
|
UTSW |
7 |
49,206,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3817:Nav2
|
UTSW |
7 |
49,114,310 (GRCm39) |
missense |
probably benign |
0.00 |
R3834:Nav2
|
UTSW |
7 |
49,195,606 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4207:Nav2
|
UTSW |
7 |
49,246,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4207:Nav2
|
UTSW |
7 |
49,222,046 (GRCm39) |
splice site |
probably null |
|
R4411:Nav2
|
UTSW |
7 |
49,047,857 (GRCm39) |
missense |
probably benign |
0.37 |
R4413:Nav2
|
UTSW |
7 |
49,047,857 (GRCm39) |
missense |
probably benign |
0.37 |
R4440:Nav2
|
UTSW |
7 |
49,225,011 (GRCm39) |
splice site |
probably benign |
|
R4440:Nav2
|
UTSW |
7 |
49,201,785 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4729:Nav2
|
UTSW |
7 |
49,102,567 (GRCm39) |
missense |
probably benign |
0.17 |
R4801:Nav2
|
UTSW |
7 |
49,195,600 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4802:Nav2
|
UTSW |
7 |
49,195,600 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4824:Nav2
|
UTSW |
7 |
49,058,749 (GRCm39) |
intron |
probably benign |
|
R4887:Nav2
|
UTSW |
7 |
49,198,182 (GRCm39) |
nonsense |
probably null |
|
R4908:Nav2
|
UTSW |
7 |
49,254,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Nav2
|
UTSW |
7 |
48,954,288 (GRCm39) |
intron |
probably benign |
|
R4965:Nav2
|
UTSW |
7 |
49,202,625 (GRCm39) |
nonsense |
probably null |
|
R5169:Nav2
|
UTSW |
7 |
49,198,231 (GRCm39) |
nonsense |
probably null |
|
R5224:Nav2
|
UTSW |
7 |
49,201,473 (GRCm39) |
missense |
probably benign |
0.00 |
R5249:Nav2
|
UTSW |
7 |
49,185,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Nav2
|
UTSW |
7 |
49,197,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Nav2
|
UTSW |
7 |
49,058,440 (GRCm39) |
small deletion |
probably benign |
|
R5320:Nav2
|
UTSW |
7 |
49,141,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5377:Nav2
|
UTSW |
7 |
49,238,908 (GRCm39) |
missense |
probably benign |
0.02 |
R5471:Nav2
|
UTSW |
7 |
49,197,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Nav2
|
UTSW |
7 |
49,206,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5832:Nav2
|
UTSW |
7 |
49,197,817 (GRCm39) |
splice site |
probably null |
|
R5884:Nav2
|
UTSW |
7 |
49,246,917 (GRCm39) |
nonsense |
probably null |
|
R5921:Nav2
|
UTSW |
7 |
48,954,324 (GRCm39) |
intron |
probably benign |
|
R6180:Nav2
|
UTSW |
7 |
49,107,915 (GRCm39) |
missense |
probably benign |
0.39 |
R6208:Nav2
|
UTSW |
7 |
49,213,851 (GRCm39) |
missense |
probably damaging |
0.99 |
R6373:Nav2
|
UTSW |
7 |
49,102,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Nav2
|
UTSW |
7 |
49,244,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Nav2
|
UTSW |
7 |
49,247,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6626:Nav2
|
UTSW |
7 |
49,244,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Nav2
|
UTSW |
7 |
49,114,652 (GRCm39) |
missense |
probably benign |
0.04 |
R6705:Nav2
|
UTSW |
7 |
49,201,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Nav2
|
UTSW |
7 |
49,107,917 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6847:Nav2
|
UTSW |
7 |
49,141,204 (GRCm39) |
missense |
probably benign |
0.14 |
R7287:Nav2
|
UTSW |
7 |
49,070,076 (GRCm39) |
missense |
probably benign |
0.01 |
R7312:Nav2
|
UTSW |
7 |
49,111,672 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7315:Nav2
|
UTSW |
7 |
49,198,037 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7337:Nav2
|
UTSW |
7 |
49,201,521 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7366:Nav2
|
UTSW |
7 |
49,203,951 (GRCm39) |
splice site |
probably null |
|
R7451:Nav2
|
UTSW |
7 |
49,202,577 (GRCm39) |
splice site |
probably null |
|
R7545:Nav2
|
UTSW |
7 |
49,232,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7706:Nav2
|
UTSW |
7 |
49,244,067 (GRCm39) |
missense |
probably benign |
0.35 |
R7730:Nav2
|
UTSW |
7 |
49,222,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7812:Nav2
|
UTSW |
7 |
49,246,921 (GRCm39) |
missense |
probably benign |
0.13 |
R8097:Nav2
|
UTSW |
7 |
49,237,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Nav2
|
UTSW |
7 |
49,201,698 (GRCm39) |
nonsense |
probably null |
|
R8119:Nav2
|
UTSW |
7 |
49,103,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R8298:Nav2
|
UTSW |
7 |
49,204,009 (GRCm39) |
critical splice donor site |
probably null |
|
R8306:Nav2
|
UTSW |
7 |
49,195,765 (GRCm39) |
missense |
probably benign |
0.33 |
R8331:Nav2
|
UTSW |
7 |
49,102,371 (GRCm39) |
missense |
probably benign |
|
R8402:Nav2
|
UTSW |
7 |
49,103,185 (GRCm39) |
missense |
probably benign |
0.43 |
R8421:Nav2
|
UTSW |
7 |
49,102,269 (GRCm39) |
missense |
probably benign |
|
R8478:Nav2
|
UTSW |
7 |
49,111,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R8724:Nav2
|
UTSW |
7 |
49,141,184 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8753:Nav2
|
UTSW |
7 |
49,102,320 (GRCm39) |
missense |
probably benign |
|
R8835:Nav2
|
UTSW |
7 |
49,248,551 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8933:Nav2
|
UTSW |
7 |
49,111,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R8957:Nav2
|
UTSW |
7 |
49,220,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Nav2
|
UTSW |
7 |
49,208,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R9095:Nav2
|
UTSW |
7 |
49,254,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Nav2
|
UTSW |
7 |
49,202,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Nav2
|
UTSW |
7 |
49,246,904 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Nav2
|
UTSW |
7 |
49,197,647 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Nav2
|
UTSW |
7 |
49,243,971 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Nav2
|
UTSW |
7 |
49,102,509 (GRCm39) |
missense |
possibly damaging |
0.47 |
|