Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730071L15Rik |
A |
G |
11: 6,150,442 (GRCm39) |
*138W |
probably null |
Het |
Abcb1a |
T |
A |
5: 8,787,773 (GRCm39) |
|
probably null |
Het |
Acp6 |
T |
C |
3: 97,079,060 (GRCm39) |
|
probably null |
Het |
Adcyap1 |
A |
T |
17: 93,511,541 (GRCm39) |
I172L |
probably benign |
Het |
Adgrf1 |
A |
C |
17: 43,606,130 (GRCm39) |
I85L |
probably benign |
Het |
Afdn |
A |
T |
17: 14,111,228 (GRCm39) |
T1604S |
probably benign |
Het |
Angpt2 |
T |
C |
8: 18,742,131 (GRCm39) |
Y475C |
probably damaging |
Het |
Ank2 |
A |
G |
3: 126,749,713 (GRCm39) |
S439P |
probably damaging |
Het |
Ank3 |
T |
A |
10: 69,812,033 (GRCm39) |
N366K |
probably damaging |
Het |
Ankrd11 |
A |
G |
8: 123,626,922 (GRCm39) |
S87P |
probably benign |
Het |
Ano7 |
T |
A |
1: 93,323,036 (GRCm39) |
S459T |
possibly damaging |
Het |
Asxl3 |
G |
A |
18: 22,656,369 (GRCm39) |
V1460M |
probably benign |
Het |
Atg16l1 |
A |
C |
1: 87,694,764 (GRCm39) |
N147T |
possibly damaging |
Het |
Atp10a |
T |
C |
7: 58,463,512 (GRCm39) |
V1015A |
probably damaging |
Het |
Atxn7 |
T |
A |
14: 14,100,401 (GRCm38) |
S696T |
probably benign |
Het |
Babam1 |
C |
T |
8: 71,852,446 (GRCm39) |
T184I |
probably benign |
Het |
Blk |
A |
G |
14: 63,618,711 (GRCm39) |
S175P |
possibly damaging |
Het |
Col5a1 |
T |
A |
2: 27,914,754 (GRCm39) |
F123L |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 48,024,480 (GRCm39) |
Y496C |
probably damaging |
Het |
Dnah3 |
A |
T |
7: 119,615,700 (GRCm39) |
Y1676* |
probably null |
Het |
Fdxacb1 |
T |
A |
9: 50,683,243 (GRCm39) |
M402K |
probably benign |
Het |
Frmd5 |
A |
G |
2: 121,393,405 (GRCm39) |
V141A |
possibly damaging |
Het |
Gapvd1 |
G |
A |
2: 34,594,504 (GRCm39) |
R685* |
probably null |
Het |
Grik2 |
A |
G |
10: 49,116,826 (GRCm39) |
L645P |
probably damaging |
Het |
H2aj |
T |
A |
6: 136,785,681 (GRCm39) |
V115E |
possibly damaging |
Het |
Hrh3 |
T |
C |
2: 179,743,061 (GRCm39) |
Y189C |
probably damaging |
Het |
Kcnc2 |
A |
G |
10: 112,108,133 (GRCm39) |
T175A |
probably benign |
Het |
Kcnv2 |
A |
G |
19: 27,300,332 (GRCm39) |
Y61C |
probably damaging |
Het |
Kif24 |
T |
C |
4: 41,394,939 (GRCm39) |
R645G |
probably damaging |
Het |
Knl1 |
A |
G |
2: 118,899,438 (GRCm39) |
I380V |
possibly damaging |
Het |
Lamb2 |
A |
G |
9: 108,364,700 (GRCm39) |
I1151M |
possibly damaging |
Het |
Leo1 |
A |
G |
9: 75,353,159 (GRCm39) |
D234G |
probably benign |
Het |
Lrp1b |
T |
G |
2: 41,388,405 (GRCm39) |
N407H |
probably benign |
Het |
Matn2 |
T |
C |
15: 34,428,831 (GRCm39) |
S732P |
probably damaging |
Het |
Mrps30 |
A |
T |
13: 118,523,431 (GRCm39) |
F114I |
possibly damaging |
Het |
Or1l8 |
T |
C |
2: 36,817,713 (GRCm39) |
N138D |
probably benign |
Het |
Or4f17-ps1 |
G |
A |
2: 111,357,793 (GRCm39) |
V45I |
probably damaging |
Het |
Or5b123 |
T |
C |
19: 13,597,066 (GRCm39) |
I180T |
probably benign |
Het |
Oxr1 |
T |
C |
15: 41,676,980 (GRCm39) |
V179A |
probably benign |
Het |
Plaur |
A |
T |
7: 24,166,141 (GRCm39) |
S71C |
possibly damaging |
Het |
Plbd2 |
T |
C |
5: 120,624,786 (GRCm39) |
N461D |
possibly damaging |
Het |
Plcb2 |
T |
A |
2: 118,549,396 (GRCm39) |
Y322F |
probably damaging |
Het |
Prkab2 |
T |
C |
3: 97,569,671 (GRCm39) |
V79A |
probably damaging |
Het |
Ptpn3 |
A |
T |
4: 57,197,568 (GRCm39) |
C774S |
probably damaging |
Het |
Ring1 |
A |
C |
17: 34,242,016 (GRCm39) |
L131R |
probably benign |
Het |
Rxfp2 |
G |
A |
5: 149,975,097 (GRCm39) |
|
probably null |
Het |
Selenbp1 |
A |
T |
3: 94,845,269 (GRCm39) |
I122F |
probably benign |
Het |
Septin7 |
A |
G |
9: 25,217,468 (GRCm39) |
H394R |
probably benign |
Het |
Slc1a7 |
G |
A |
4: 107,864,758 (GRCm39) |
V266I |
probably damaging |
Het |
Slc2a10 |
A |
G |
2: 165,359,578 (GRCm39) |
T481A |
probably benign |
Het |
Spmap2l |
T |
C |
5: 77,185,200 (GRCm39) |
|
probably null |
Het |
Tapbp |
A |
G |
17: 34,144,596 (GRCm39) |
M231V |
probably benign |
Het |
Tbxas1 |
A |
T |
6: 38,999,981 (GRCm39) |
N256I |
probably benign |
Het |
Uimc1 |
A |
G |
13: 55,240,998 (GRCm39) |
I30T |
probably damaging |
Het |
Usp48 |
C |
A |
4: 137,377,669 (GRCm39) |
N231K |
probably benign |
Het |
Znrf3 |
A |
T |
11: 5,233,422 (GRCm39) |
C212S |
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 |
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 |
|