Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,622,212 (GRCm39) |
V372F |
probably benign |
Het |
Adcy10 |
G |
A |
1: 165,347,464 (GRCm39) |
C393Y |
probably damaging |
Het |
Adgrg7 |
A |
C |
16: 56,550,669 (GRCm39) |
I681S |
possibly damaging |
Het |
Akap8l |
T |
C |
17: 32,540,485 (GRCm39) |
|
probably benign |
Het |
Akr1a1 |
A |
T |
4: 116,497,092 (GRCm39) |
V156E |
probably damaging |
Het |
Alk |
T |
G |
17: 72,202,734 (GRCm39) |
D1167A |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,620,453 (GRCm39) |
|
probably null |
Het |
Aspm |
T |
A |
1: 139,385,221 (GRCm39) |
N288K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,398,133 (GRCm39) |
|
probably null |
Het |
Asxl2 |
G |
A |
12: 3,524,618 (GRCm39) |
|
probably null |
Het |
Atp6v0a1 |
A |
G |
11: 100,946,413 (GRCm39) |
H802R |
probably damaging |
Het |
B4galnt1 |
A |
G |
10: 127,007,691 (GRCm39) |
T531A |
possibly damaging |
Het |
Cecr2 |
A |
G |
6: 120,733,530 (GRCm39) |
N506D |
possibly damaging |
Het |
Crebrf |
T |
C |
17: 26,978,839 (GRCm39) |
V509A |
probably damaging |
Het |
Cyp4f40 |
A |
T |
17: 32,894,590 (GRCm39) |
I413F |
probably null |
Het |
Defb12 |
C |
A |
8: 19,164,342 (GRCm39) |
|
probably null |
Het |
Dnah2 |
T |
C |
11: 69,312,674 (GRCm39) |
E4297G |
probably damaging |
Het |
Dpysl5 |
A |
T |
5: 30,948,857 (GRCm39) |
N371Y |
probably damaging |
Het |
Eef1d |
G |
T |
15: 75,775,038 (GRCm39) |
T207N |
probably benign |
Het |
Esrrb |
C |
T |
12: 86,565,783 (GRCm39) |
Q416* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,536,222 (GRCm39) |
L284P |
probably damaging |
Het |
Fat3 |
T |
A |
9: 16,287,739 (GRCm39) |
I595F |
probably benign |
Het |
Gm9920 |
A |
G |
15: 54,972,371 (GRCm39) |
|
probably benign |
Het |
Hephl1 |
T |
C |
9: 14,981,084 (GRCm39) |
K783E |
probably damaging |
Het |
Irs2 |
A |
G |
8: 11,055,277 (GRCm39) |
S1052P |
probably benign |
Het |
Kctd18 |
T |
C |
1: 58,002,252 (GRCm39) |
I192V |
probably benign |
Het |
Lama3 |
A |
G |
18: 12,586,803 (GRCm39) |
D722G |
probably damaging |
Het |
Lepr |
T |
C |
4: 101,672,216 (GRCm39) |
V1080A |
possibly damaging |
Het |
Lpin1 |
C |
T |
12: 16,613,656 (GRCm39) |
G504S |
probably damaging |
Het |
Lrit2 |
A |
C |
14: 36,791,140 (GRCm39) |
Q273P |
possibly damaging |
Het |
Mlkl |
T |
A |
8: 112,054,569 (GRCm39) |
E189D |
probably benign |
Het |
Mttp |
C |
T |
3: 137,810,790 (GRCm39) |
R608H |
probably benign |
Het |
Nav2 |
T |
C |
7: 49,238,908 (GRCm39) |
V2011A |
probably benign |
Het |
Nos2 |
A |
T |
11: 78,848,317 (GRCm39) |
I1075F |
probably benign |
Het |
Npat |
A |
G |
9: 53,461,336 (GRCm39) |
|
probably null |
Het |
Nucks1 |
T |
C |
1: 131,846,771 (GRCm39) |
F16L |
probably damaging |
Het |
Nus1 |
T |
C |
10: 52,305,309 (GRCm39) |
S150P |
possibly damaging |
Het |
Odad1 |
C |
T |
7: 45,591,506 (GRCm39) |
R257* |
probably null |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or4c123 |
G |
T |
2: 89,127,506 (GRCm39) |
T36K |
probably damaging |
Het |
Or8b35 |
A |
T |
9: 37,903,908 (GRCm39) |
Y40F |
probably benign |
Het |
Pclo |
A |
G |
5: 14,731,367 (GRCm39) |
T3290A |
unknown |
Het |
Pign |
A |
T |
1: 105,585,537 (GRCm39) |
F4Y |
probably benign |
Het |
Rfx4 |
A |
G |
10: 84,696,406 (GRCm39) |
N233D |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,397,652 (GRCm39) |
M1325L |
possibly damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Scaf11 |
T |
A |
15: 96,315,001 (GRCm39) |
H1227L |
possibly damaging |
Het |
Sec31b |
G |
T |
19: 44,507,076 (GRCm39) |
P840T |
probably damaging |
Het |
Slc16a9 |
T |
A |
10: 70,118,958 (GRCm39) |
L426I |
probably damaging |
Het |
Slc22a30 |
G |
A |
19: 8,321,757 (GRCm39) |
Q436* |
probably null |
Het |
Slc34a1 |
T |
C |
13: 23,996,575 (GRCm39) |
S27P |
probably damaging |
Het |
Tacc1 |
A |
G |
8: 25,672,299 (GRCm39) |
S310P |
possibly damaging |
Het |
Tmem245 |
G |
A |
4: 56,947,084 (GRCm39) |
R110C |
probably damaging |
Het |
Trip12 |
T |
C |
1: 84,735,152 (GRCm39) |
Y953C |
probably damaging |
Het |
Trpm7 |
C |
A |
2: 126,684,775 (GRCm39) |
|
probably null |
Het |
Ush2a |
G |
A |
1: 188,644,320 (GRCm39) |
V4561I |
probably benign |
Het |
Vmn1r192 |
C |
T |
13: 22,371,801 (GRCm39) |
V140I |
probably benign |
Het |
Vmn2r66 |
A |
T |
7: 84,656,026 (GRCm39) |
I330N |
probably damaging |
Het |
Vmn2r99 |
T |
C |
17: 19,599,531 (GRCm39) |
V405A |
probably damaging |
Het |
Wdhd1 |
A |
C |
14: 47,509,678 (GRCm39) |
V172G |
probably benign |
Het |
Zfp446 |
T |
C |
7: 12,716,178 (GRCm39) |
L283P |
possibly damaging |
Het |
Zfp82 |
T |
C |
7: 29,756,591 (GRCm39) |
K164E |
probably damaging |
Het |
|
Other mutations in Zfhx3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Zfhx3
|
APN |
8 |
109,520,226 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01946:Zfhx3
|
APN |
8 |
109,660,561 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01973:Zfhx3
|
APN |
8 |
109,673,825 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01983:Zfhx3
|
APN |
8 |
109,673,866 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02151:Zfhx3
|
APN |
8 |
109,520,515 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02405:Zfhx3
|
APN |
8 |
109,682,374 (GRCm39) |
missense |
unknown |
|
IGL02406:Zfhx3
|
APN |
8 |
109,682,374 (GRCm39) |
missense |
unknown |
|
IGL02408:Zfhx3
|
APN |
8 |
109,682,004 (GRCm39) |
splice site |
probably benign |
|
IGL02549:Zfhx3
|
APN |
8 |
109,527,141 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02601:Zfhx3
|
APN |
8 |
109,583,462 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Zfhx3
|
APN |
8 |
109,520,167 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03027:Zfhx3
|
APN |
8 |
109,519,820 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03053:Zfhx3
|
APN |
8 |
109,673,132 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03168:Zfhx3
|
APN |
8 |
109,673,132 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03194:Zfhx3
|
APN |
8 |
109,521,359 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03248:Zfhx3
|
APN |
8 |
109,673,182 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Zfhx3
|
UTSW |
8 |
109,682,726 (GRCm39) |
small insertion |
probably benign |
|
FR4589:Zfhx3
|
UTSW |
8 |
109,682,733 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfhx3
|
UTSW |
8 |
109,682,735 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfhx3
|
UTSW |
8 |
109,682,734 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Zfhx3
|
UTSW |
8 |
109,682,720 (GRCm39) |
small insertion |
probably benign |
|
G5030:Zfhx3
|
UTSW |
8 |
109,678,091 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0016:Zfhx3
|
UTSW |
8 |
109,676,810 (GRCm39) |
missense |
probably benign |
0.02 |
R0090:Zfhx3
|
UTSW |
8 |
109,676,689 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0330:Zfhx3
|
UTSW |
8 |
109,675,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R0332:Zfhx3
|
UTSW |
8 |
109,673,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0398:Zfhx3
|
UTSW |
8 |
109,677,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R0539:Zfhx3
|
UTSW |
8 |
109,527,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Zfhx3
|
UTSW |
8 |
109,520,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Zfhx3
|
UTSW |
8 |
109,675,599 (GRCm39) |
nonsense |
probably null |
|
R0614:Zfhx3
|
UTSW |
8 |
109,675,171 (GRCm39) |
missense |
probably benign |
0.03 |
R0653:Zfhx3
|
UTSW |
8 |
109,673,440 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0718:Zfhx3
|
UTSW |
8 |
109,682,282 (GRCm39) |
missense |
unknown |
|
R0825:Zfhx3
|
UTSW |
8 |
109,675,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R1143:Zfhx3
|
UTSW |
8 |
109,521,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R1319:Zfhx3
|
UTSW |
8 |
109,660,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R1347:Zfhx3
|
UTSW |
8 |
109,527,330 (GRCm39) |
splice site |
probably benign |
|
R1412:Zfhx3
|
UTSW |
8 |
109,641,199 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1447:Zfhx3
|
UTSW |
8 |
109,675,076 (GRCm39) |
missense |
probably benign |
0.03 |
R1530:Zfhx3
|
UTSW |
8 |
109,675,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Zfhx3
|
UTSW |
8 |
109,682,494 (GRCm39) |
missense |
unknown |
|
R1764:Zfhx3
|
UTSW |
8 |
109,678,276 (GRCm39) |
missense |
probably benign |
0.18 |
R1781:Zfhx3
|
UTSW |
8 |
109,520,167 (GRCm39) |
missense |
probably benign |
0.01 |
R1917:Zfhx3
|
UTSW |
8 |
109,682,880 (GRCm39) |
missense |
unknown |
|
R1956:Zfhx3
|
UTSW |
8 |
109,520,774 (GRCm39) |
missense |
probably benign |
0.02 |
R2049:Zfhx3
|
UTSW |
8 |
109,671,809 (GRCm39) |
missense |
probably benign |
0.01 |
R2196:Zfhx3
|
UTSW |
8 |
109,526,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R3085:Zfhx3
|
UTSW |
8 |
109,682,664 (GRCm39) |
missense |
unknown |
|
R3765:Zfhx3
|
UTSW |
8 |
109,519,394 (GRCm39) |
missense |
probably damaging |
0.97 |
R4162:Zfhx3
|
UTSW |
8 |
109,683,619 (GRCm39) |
missense |
unknown |
|
R4243:Zfhx3
|
UTSW |
8 |
109,518,952 (GRCm39) |
missense |
probably damaging |
0.97 |
R4380:Zfhx3
|
UTSW |
8 |
109,683,022 (GRCm39) |
missense |
unknown |
|
R4433:Zfhx3
|
UTSW |
8 |
109,682,269 (GRCm39) |
missense |
unknown |
|
R4509:Zfhx3
|
UTSW |
8 |
109,520,411 (GRCm39) |
missense |
probably benign |
0.01 |
R4731:Zfhx3
|
UTSW |
8 |
109,682,716 (GRCm39) |
missense |
unknown |
|
R4788:Zfhx3
|
UTSW |
8 |
109,520,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Zfhx3
|
UTSW |
8 |
109,674,593 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4893:Zfhx3
|
UTSW |
8 |
109,683,639 (GRCm39) |
missense |
unknown |
|
R4907:Zfhx3
|
UTSW |
8 |
109,519,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R4935:Zfhx3
|
UTSW |
8 |
109,674,482 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4943:Zfhx3
|
UTSW |
8 |
109,674,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R5154:Zfhx3
|
UTSW |
8 |
109,527,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Zfhx3
|
UTSW |
8 |
109,673,446 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5434:Zfhx3
|
UTSW |
8 |
109,519,031 (GRCm39) |
missense |
probably damaging |
0.99 |
R5445:Zfhx3
|
UTSW |
8 |
109,682,842 (GRCm39) |
missense |
unknown |
|
R5541:Zfhx3
|
UTSW |
8 |
109,675,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R5571:Zfhx3
|
UTSW |
8 |
109,682,623 (GRCm39) |
missense |
unknown |
|
R5700:Zfhx3
|
UTSW |
8 |
109,660,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Zfhx3
|
UTSW |
8 |
109,526,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R5867:Zfhx3
|
UTSW |
8 |
109,520,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Zfhx3
|
UTSW |
8 |
109,520,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5922:Zfhx3
|
UTSW |
8 |
109,673,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5972:Zfhx3
|
UTSW |
8 |
109,677,483 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6020:Zfhx3
|
UTSW |
8 |
109,519,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Zfhx3
|
UTSW |
8 |
109,520,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R6113:Zfhx3
|
UTSW |
8 |
109,674,053 (GRCm39) |
missense |
probably benign |
0.04 |
R6253:Zfhx3
|
UTSW |
8 |
109,682,020 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6356:Zfhx3
|
UTSW |
8 |
109,673,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6800:Zfhx3
|
UTSW |
8 |
109,676,149 (GRCm39) |
missense |
probably benign |
0.20 |
R6829:Zfhx3
|
UTSW |
8 |
109,676,915 (GRCm39) |
missense |
probably damaging |
0.98 |
R6872:Zfhx3
|
UTSW |
8 |
109,527,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Zfhx3
|
UTSW |
8 |
109,527,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Zfhx3
|
UTSW |
8 |
109,527,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R6921:Zfhx3
|
UTSW |
8 |
109,678,024 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6925:Zfhx3
|
UTSW |
8 |
109,683,453 (GRCm39) |
missense |
unknown |
|
R6927:Zfhx3
|
UTSW |
8 |
109,683,453 (GRCm39) |
missense |
unknown |
|
R7152:Zfhx3
|
UTSW |
8 |
109,674,839 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7169:Zfhx3
|
UTSW |
8 |
109,678,030 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7214:Zfhx3
|
UTSW |
8 |
109,675,493 (GRCm39) |
missense |
probably damaging |
0.98 |
R7378:Zfhx3
|
UTSW |
8 |
109,519,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R7391:Zfhx3
|
UTSW |
8 |
109,674,475 (GRCm39) |
missense |
probably damaging |
0.96 |
R7442:Zfhx3
|
UTSW |
8 |
109,519,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R7636:Zfhx3
|
UTSW |
8 |
109,673,441 (GRCm39) |
missense |
probably benign |
0.25 |
R7649:Zfhx3
|
UTSW |
8 |
109,678,276 (GRCm39) |
missense |
probably benign |
0.18 |
R7699:Zfhx3
|
UTSW |
8 |
109,677,754 (GRCm39) |
missense |
probably benign |
0.18 |
R7728:Zfhx3
|
UTSW |
8 |
109,678,201 (GRCm39) |
missense |
probably benign |
0.01 |
R7780:Zfhx3
|
UTSW |
8 |
109,678,283 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7904:Zfhx3
|
UTSW |
8 |
109,677,695 (GRCm39) |
missense |
probably damaging |
0.98 |
R8032:Zfhx3
|
UTSW |
8 |
109,677,854 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8158:Zfhx3
|
UTSW |
8 |
109,675,353 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8163:Zfhx3
|
UTSW |
8 |
109,675,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R8215:Zfhx3
|
UTSW |
8 |
109,677,349 (GRCm39) |
missense |
probably benign |
|
R8217:Zfhx3
|
UTSW |
8 |
109,677,349 (GRCm39) |
missense |
probably benign |
|
R8218:Zfhx3
|
UTSW |
8 |
109,677,349 (GRCm39) |
missense |
probably benign |
|
R8369:Zfhx3
|
UTSW |
8 |
109,583,448 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8424:Zfhx3
|
UTSW |
8 |
109,583,385 (GRCm39) |
missense |
probably damaging |
0.98 |
R8482:Zfhx3
|
UTSW |
8 |
109,674,511 (GRCm39) |
missense |
probably benign |
0.02 |
R8504:Zfhx3
|
UTSW |
8 |
109,583,549 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8871:Zfhx3
|
UTSW |
8 |
109,676,867 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9144:Zfhx3
|
UTSW |
8 |
109,676,794 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9202:Zfhx3
|
UTSW |
8 |
109,677,920 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9213:Zfhx3
|
UTSW |
8 |
109,676,756 (GRCm39) |
missense |
probably benign |
0.18 |
R9218:Zfhx3
|
UTSW |
8 |
109,520,501 (GRCm39) |
missense |
probably benign |
0.17 |
R9370:Zfhx3
|
UTSW |
8 |
109,521,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R9422:Zfhx3
|
UTSW |
8 |
109,430,850 (GRCm39) |
start gained |
probably benign |
|
R9530:Zfhx3
|
UTSW |
8 |
109,527,010 (GRCm39) |
missense |
probably damaging |
1.00 |
RF027:Zfhx3
|
UTSW |
8 |
109,682,730 (GRCm39) |
small insertion |
probably benign |
|
RF028:Zfhx3
|
UTSW |
8 |
109,682,728 (GRCm39) |
small insertion |
probably benign |
|
RF029:Zfhx3
|
UTSW |
8 |
109,682,724 (GRCm39) |
small insertion |
probably benign |
|
RF031:Zfhx3
|
UTSW |
8 |
109,682,730 (GRCm39) |
small insertion |
probably benign |
|
RF032:Zfhx3
|
UTSW |
8 |
109,682,724 (GRCm39) |
small insertion |
probably benign |
|
RF037:Zfhx3
|
UTSW |
8 |
109,682,730 (GRCm39) |
nonsense |
probably null |
|
RF038:Zfhx3
|
UTSW |
8 |
109,682,733 (GRCm39) |
small insertion |
probably benign |
|
RF040:Zfhx3
|
UTSW |
8 |
109,682,733 (GRCm39) |
small insertion |
probably benign |
|
RF042:Zfhx3
|
UTSW |
8 |
109,682,730 (GRCm39) |
small insertion |
probably benign |
|
RF042:Zfhx3
|
UTSW |
8 |
109,682,720 (GRCm39) |
small insertion |
probably benign |
|
RF054:Zfhx3
|
UTSW |
8 |
109,682,728 (GRCm39) |
small insertion |
probably benign |
|
RF060:Zfhx3
|
UTSW |
8 |
109,682,720 (GRCm39) |
small insertion |
probably benign |
|
X0019:Zfhx3
|
UTSW |
8 |
109,678,285 (GRCm39) |
missense |
probably benign |
0.00 |
X0026:Zfhx3
|
UTSW |
8 |
109,675,777 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Zfhx3
|
UTSW |
8 |
109,677,989 (GRCm39) |
missense |
possibly damaging |
0.72 |
Z1176:Zfhx3
|
UTSW |
8 |
109,527,081 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfhx3
|
UTSW |
8 |
109,520,555 (GRCm39) |
missense |
probably benign |
0.09 |
|