Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
A |
5: 8,984,320 (GRCm39) |
N683K |
probably benign |
Het |
Atad2b |
T |
A |
12: 5,060,351 (GRCm39) |
H915Q |
probably benign |
Het |
Bltp2 |
T |
C |
11: 78,160,367 (GRCm39) |
S609P |
probably damaging |
Het |
Camk1d |
G |
T |
2: 5,449,908 (GRCm39) |
P91Q |
probably benign |
Het |
Camk1d |
G |
C |
2: 5,449,910 (GRCm39) |
S90R |
probably damaging |
Het |
Card11 |
T |
C |
5: 140,885,524 (GRCm39) |
E345G |
probably damaging |
Het |
Ccpg1 |
G |
T |
9: 72,920,526 (GRCm39) |
V714L |
possibly damaging |
Het |
Chst9 |
T |
C |
18: 15,586,254 (GRCm39) |
E103G |
possibly damaging |
Het |
Cnga1 |
C |
T |
5: 72,762,615 (GRCm39) |
V300I |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,159,337 (GRCm39) |
Y1295C |
probably damaging |
Het |
Dnah5 |
A |
G |
15: 28,402,014 (GRCm39) |
T3392A |
probably benign |
Het |
Elp3 |
C |
A |
14: 65,785,439 (GRCm39) |
R473L |
probably damaging |
Het |
Epgn |
T |
A |
5: 91,181,807 (GRCm39) |
I145N |
probably benign |
Het |
Fam107b |
G |
A |
2: 3,779,457 (GRCm39) |
G220D |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,257,383 (GRCm39) |
V328A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,639,481 (GRCm39) |
I1770N |
probably damaging |
Het |
Fndc1 |
T |
A |
17: 7,988,585 (GRCm39) |
Y1159F |
unknown |
Het |
Frem2 |
A |
G |
3: 53,444,679 (GRCm39) |
L2484P |
probably damaging |
Het |
Grk2 |
C |
T |
19: 4,340,496 (GRCm39) |
R295H |
probably damaging |
Het |
Gtf3c1 |
A |
T |
7: 125,243,237 (GRCm39) |
V1789D |
possibly damaging |
Het |
Hmgcl |
T |
C |
4: 135,677,898 (GRCm39) |
V33A |
probably damaging |
Het |
Ighv7-1 |
A |
G |
12: 113,860,239 (GRCm39) |
F51S |
probably damaging |
Het |
Kcna6 |
A |
G |
6: 126,716,688 (GRCm39) |
L67P |
probably damaging |
Het |
Lamc1 |
A |
T |
1: 153,123,030 (GRCm39) |
V720E |
probably benign |
Het |
Lrch1 |
T |
C |
14: 75,054,558 (GRCm39) |
D312G |
probably damaging |
Het |
Mix23 |
A |
G |
16: 35,905,427 (GRCm39) |
N63S |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,206,794 (GRCm39) |
T1540A |
probably damaging |
Het |
Nisch |
A |
T |
14: 30,913,373 (GRCm39) |
|
probably benign |
Het |
Nos1ap |
T |
A |
1: 170,176,968 (GRCm39) |
K145M |
probably damaging |
Het |
Npc1l1 |
A |
G |
11: 6,177,839 (GRCm39) |
Y524H |
probably damaging |
Het |
Nrap |
T |
C |
19: 56,377,916 (GRCm39) |
T25A |
possibly damaging |
Het |
Nusap1 |
A |
G |
2: 119,477,580 (GRCm39) |
K363R |
probably damaging |
Het |
Or5ar1 |
T |
C |
2: 85,671,656 (GRCm39) |
T160A |
probably damaging |
Het |
Or5b124 |
A |
G |
19: 13,611,357 (GRCm39) |
E294G |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,212,390 (GRCm39) |
L298Q |
probably damaging |
Het |
Pde4d |
T |
C |
13: 110,074,547 (GRCm39) |
I384T |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,593,875 (GRCm39) |
R1413* |
probably null |
Het |
Plcd3 |
T |
A |
11: 102,964,592 (GRCm39) |
Y593F |
possibly damaging |
Het |
Plxna1 |
A |
T |
6: 89,310,087 (GRCm39) |
I1026N |
possibly damaging |
Het |
Podxl |
T |
A |
6: 31,501,329 (GRCm39) |
I409F |
probably damaging |
Het |
Polq |
A |
C |
16: 36,837,625 (GRCm39) |
Q179P |
probably benign |
Het |
Pomt1 |
T |
C |
2: 32,137,602 (GRCm39) |
V401A |
probably damaging |
Het |
Qdpr |
C |
T |
5: 45,596,727 (GRCm39) |
G146S |
probably damaging |
Het |
Shc4 |
T |
A |
2: 125,512,218 (GRCm39) |
Q2L |
probably damaging |
Het |
Skint8 |
T |
A |
4: 111,807,387 (GRCm39) |
C358S |
probably benign |
Het |
Smc5 |
T |
C |
19: 23,221,467 (GRCm39) |
E354G |
possibly damaging |
Het |
Snx30 |
T |
C |
4: 59,868,275 (GRCm39) |
V129A |
probably damaging |
Het |
Sp110 |
G |
C |
1: 85,504,923 (GRCm39) |
|
probably benign |
Het |
Spag6 |
T |
A |
2: 18,703,613 (GRCm39) |
|
probably benign |
Het |
Trim28 |
T |
A |
7: 12,763,036 (GRCm39) |
Y450N |
probably benign |
Het |
Trip11 |
C |
T |
12: 101,851,924 (GRCm39) |
W428* |
probably null |
Het |
Umodl1 |
T |
A |
17: 31,213,761 (GRCm39) |
V966E |
probably damaging |
Het |
Utf1 |
A |
G |
7: 139,524,704 (GRCm39) |
|
probably benign |
Het |
Vmn1r72 |
T |
C |
7: 11,403,776 (GRCm39) |
Y224C |
probably damaging |
Het |
Whrn |
A |
G |
4: 63,334,825 (GRCm39) |
S748P |
probably damaging |
Het |
Zbtb41 |
T |
A |
1: 139,359,816 (GRCm39) |
|
probably null |
Het |
Zfp456 |
A |
T |
13: 67,514,359 (GRCm39) |
I449K |
probably benign |
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 |
R5377:Zfhx3
|
UTSW |
8 |
109,677,817 (GRCm39) |
missense |
possibly damaging |
0.95 |
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 |
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 |
|