Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,333,959 (GRCm39) |
V1181G |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,217,915 (GRCm39) |
I291F |
probably damaging |
Het |
Aspm |
G |
C |
1: 139,407,282 (GRCm39) |
Q2056H |
probably benign |
Het |
C7 |
A |
T |
15: 5,076,406 (GRCm39) |
V122E |
probably benign |
Het |
Casp12 |
A |
T |
9: 5,352,844 (GRCm39) |
Q152L |
probably null |
Het |
Cdh16 |
T |
A |
8: 105,344,264 (GRCm39) |
T92S |
probably benign |
Het |
Chrd |
G |
C |
16: 20,553,058 (GRCm39) |
V162L |
possibly damaging |
Het |
Cpne8 |
A |
G |
15: 90,385,608 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
T |
C |
13: 113,502,639 (GRCm39) |
Y115H |
probably damaging |
Het |
Cyp2j7 |
T |
A |
4: 96,090,384 (GRCm39) |
I347F |
probably damaging |
Het |
Cyp4a10 |
A |
T |
4: 115,378,304 (GRCm39) |
Q130L |
probably damaging |
Het |
Dach1 |
C |
T |
14: 98,406,184 (GRCm39) |
G188R |
probably damaging |
Het |
Dgkd |
T |
C |
1: 87,845,674 (GRCm39) |
S294P |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,882,290 (GRCm39) |
I621V |
probably benign |
Het |
Dync2h1 |
A |
G |
9: 7,144,346 (GRCm39) |
|
probably benign |
Het |
Echdc1 |
A |
T |
10: 29,198,417 (GRCm39) |
|
probably benign |
Het |
Elovl3 |
T |
A |
19: 46,120,597 (GRCm39) |
F30Y |
probably damaging |
Het |
Fa2h |
T |
C |
8: 112,120,146 (GRCm39) |
Y80C |
probably damaging |
Het |
Fgd3 |
C |
T |
13: 49,450,085 (GRCm39) |
D55N |
probably benign |
Het |
Fhod1 |
T |
C |
8: 106,058,287 (GRCm39) |
E823G |
possibly damaging |
Het |
Gapvd1 |
A |
G |
2: 34,589,925 (GRCm39) |
|
probably benign |
Het |
Gm17067 |
A |
T |
7: 42,358,046 (GRCm39) |
I152K |
probably benign |
Het |
Gvin3 |
G |
A |
7: 106,202,453 (GRCm39) |
L264F |
probably benign |
Het |
Kif27 |
A |
G |
13: 58,502,528 (GRCm39) |
V50A |
probably damaging |
Het |
Kpna2 |
T |
C |
11: 106,881,912 (GRCm39) |
T305A |
probably benign |
Het |
Krtap22-2 |
A |
G |
16: 88,807,407 (GRCm39) |
|
probably benign |
Het |
Lrp2bp |
T |
A |
8: 46,465,068 (GRCm39) |
F62L |
probably damaging |
Het |
Marf1 |
G |
A |
16: 13,970,129 (GRCm39) |
H197Y |
probably damaging |
Het |
Mob3b |
A |
G |
4: 35,083,947 (GRCm39) |
F81L |
probably benign |
Het |
Mon2 |
C |
T |
10: 122,871,451 (GRCm39) |
V389M |
probably damaging |
Het |
Myef2l |
A |
T |
3: 10,154,379 (GRCm39) |
M383L |
possibly damaging |
Het |
Myh8 |
A |
G |
11: 67,189,351 (GRCm39) |
K1176E |
probably damaging |
Het |
Naf1 |
T |
C |
8: 67,341,707 (GRCm39) |
|
probably benign |
Het |
Nckap1l |
A |
G |
15: 103,384,063 (GRCm39) |
T554A |
probably benign |
Het |
Oog3 |
A |
G |
4: 143,884,641 (GRCm39) |
Y432H |
probably damaging |
Het |
Paxbp1 |
A |
T |
16: 90,832,924 (GRCm39) |
|
probably benign |
Het |
Phf20 |
A |
T |
2: 156,109,114 (GRCm39) |
K154* |
probably null |
Het |
Pip4p1 |
C |
T |
14: 51,166,351 (GRCm39) |
R213Q |
probably damaging |
Het |
Plekhj1 |
T |
C |
10: 80,632,250 (GRCm39) |
D74G |
possibly damaging |
Het |
Plpp4 |
T |
C |
7: 128,925,148 (GRCm39) |
C128R |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,145,689 (GRCm39) |
|
probably null |
Het |
Sh3rf1 |
T |
A |
8: 61,827,172 (GRCm39) |
M642K |
probably benign |
Het |
Slc7a1 |
A |
G |
5: 148,271,393 (GRCm39) |
V522A |
probably benign |
Het |
Sorbs1 |
A |
G |
19: 40,303,182 (GRCm39) |
|
probably benign |
Het |
Spry2 |
C |
T |
14: 106,130,731 (GRCm39) |
V152M |
probably benign |
Het |
Srgap2 |
A |
G |
1: 131,277,200 (GRCm39) |
M349T |
possibly damaging |
Het |
Stag3 |
A |
G |
5: 138,289,643 (GRCm39) |
H271R |
possibly damaging |
Het |
Stat4 |
T |
C |
1: 52,107,939 (GRCm39) |
V136A |
probably benign |
Het |
Stc2 |
A |
T |
11: 31,310,177 (GRCm39) |
D286E |
probably benign |
Het |
Stk31 |
T |
C |
6: 49,414,311 (GRCm39) |
Y482H |
probably damaging |
Het |
Tasor2 |
A |
C |
13: 3,635,170 (GRCm39) |
|
probably null |
Het |
Ticrr |
C |
T |
7: 79,343,540 (GRCm39) |
P1135L |
probably benign |
Het |
Trim27 |
A |
T |
13: 21,375,399 (GRCm39) |
E310V |
probably benign |
Het |
Uvrag |
T |
C |
7: 98,641,188 (GRCm39) |
K284R |
probably benign |
Het |
Vmn1r78 |
A |
C |
7: 11,887,279 (GRCm39) |
S297R |
probably benign |
Het |
Xylt2 |
A |
G |
11: 94,560,466 (GRCm39) |
S270P |
probably damaging |
Het |
Zkscan2 |
C |
A |
7: 123,099,219 (GRCm39) |
|
probably benign |
Het |
Zwint |
T |
C |
10: 72,493,030 (GRCm39) |
|
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 |
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 |
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 |
|