Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad12 |
A |
G |
5: 121,742,357 (GRCm39) |
I417T |
possibly damaging |
Het |
Adcy9 |
T |
C |
16: 4,106,088 (GRCm39) |
T1009A |
probably benign |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Baat |
T |
C |
4: 49,490,425 (GRCm39) |
|
probably benign |
Het |
Bpi |
T |
A |
2: 158,115,072 (GRCm39) |
L311* |
probably null |
Het |
Brd2 |
A |
C |
17: 34,332,233 (GRCm39) |
F294L |
probably damaging |
Het |
Carmil1 |
T |
A |
13: 24,209,850 (GRCm39) |
E804D |
probably benign |
Het |
Cd209g |
A |
T |
8: 4,184,785 (GRCm39) |
|
probably benign |
Het |
Cfi |
A |
G |
3: 129,668,635 (GRCm39) |
I554V |
probably benign |
Het |
Clvs2 |
G |
C |
10: 33,498,542 (GRCm39) |
S129R |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,268,268 (GRCm39) |
S2897P |
probably damaging |
Het |
Efcab7 |
T |
C |
4: 99,761,877 (GRCm39) |
|
probably benign |
Het |
Fbxo2 |
T |
C |
4: 148,249,367 (GRCm39) |
|
probably null |
Het |
Fgfr2 |
C |
A |
7: 129,797,993 (GRCm39) |
R400L |
probably damaging |
Het |
Hsd17b14 |
T |
C |
7: 45,205,834 (GRCm39) |
|
probably benign |
Het |
Il23r |
T |
C |
6: 67,463,206 (GRCm39) |
N96D |
probably damaging |
Het |
Ints13 |
T |
A |
6: 146,476,285 (GRCm39) |
|
probably benign |
Het |
Khdc4 |
T |
A |
3: 88,619,046 (GRCm39) |
S583R |
probably damaging |
Het |
Lig1 |
A |
G |
7: 13,041,495 (GRCm39) |
I776V |
possibly damaging |
Het |
Madd |
T |
C |
2: 90,993,083 (GRCm39) |
I997V |
probably benign |
Het |
Mgat4b |
C |
T |
11: 50,121,826 (GRCm39) |
H116Y |
possibly damaging |
Het |
Myo5b |
A |
C |
18: 74,834,751 (GRCm39) |
D937A |
probably benign |
Het |
Nox3 |
T |
C |
17: 3,685,556 (GRCm39) |
N584S |
probably benign |
Het |
Ogfr |
A |
G |
2: 180,232,830 (GRCm39) |
|
probably null |
Het |
Or11g25 |
T |
A |
14: 50,723,791 (GRCm39) |
M292K |
probably benign |
Het |
Or13p3 |
T |
C |
4: 118,567,078 (GRCm39) |
V158A |
probably benign |
Het |
Or8b1b |
T |
C |
9: 38,375,958 (GRCm39) |
I207T |
probably benign |
Het |
Osbpl6 |
G |
T |
2: 76,423,758 (GRCm39) |
V728F |
probably benign |
Het |
Picalm |
T |
A |
7: 89,831,525 (GRCm39) |
S453T |
probably benign |
Het |
Piezo1 |
A |
G |
8: 123,228,354 (GRCm39) |
L310P |
probably damaging |
Het |
Pitrm1 |
C |
T |
13: 6,599,604 (GRCm39) |
|
probably benign |
Het |
Pkd1 |
T |
C |
17: 24,805,197 (GRCm39) |
F3250L |
probably damaging |
Het |
Plekha4 |
C |
T |
7: 45,193,373 (GRCm39) |
R376* |
probably null |
Het |
Pnma8b |
A |
T |
7: 16,679,474 (GRCm39) |
S153C |
unknown |
Het |
Rp1l1 |
C |
T |
14: 64,259,744 (GRCm39) |
R129W |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,690,108 (GRCm39) |
V1147A |
probably damaging |
Het |
Sema3d |
G |
A |
5: 12,620,953 (GRCm39) |
V520I |
probably benign |
Het |
Sgsm1 |
A |
G |
5: 113,427,136 (GRCm39) |
|
probably benign |
Het |
Slc13a2 |
A |
G |
11: 78,297,694 (GRCm39) |
V58A |
probably damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,510 (GRCm39) |
|
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,074,690 (GRCm39) |
|
probably benign |
Het |
Tab1 |
G |
T |
15: 80,040,094 (GRCm39) |
A305S |
probably benign |
Het |
Tmem30a |
T |
A |
9: 79,678,576 (GRCm39) |
T327S |
probably benign |
Het |
Tpr |
A |
C |
1: 150,293,164 (GRCm39) |
E863A |
possibly damaging |
Het |
Upk3bl |
A |
G |
5: 136,088,969 (GRCm39) |
N161D |
probably benign |
Het |
Ush1c |
T |
A |
7: 45,874,979 (GRCm39) |
I131F |
probably benign |
Het |
Wdfy4 |
C |
A |
14: 32,800,200 (GRCm39) |
R1975S |
possibly damaging |
Het |
Zbtb18 |
C |
T |
1: 177,275,501 (GRCm39) |
A287V |
probably benign |
Het |
Zfp712 |
T |
C |
13: 67,189,256 (GRCm39) |
T424A |
probably benign |
Het |
Zfp791 |
G |
T |
8: 85,838,862 (GRCm39) |
Y56* |
probably null |
Het |
|
Other mutations in Myh11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01362:Myh11
|
APN |
16 |
14,095,586 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01398:Myh11
|
APN |
16 |
14,019,964 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01646:Myh11
|
APN |
16 |
14,039,639 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02470:Myh11
|
APN |
16 |
14,035,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02680:Myh11
|
APN |
16 |
14,027,384 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02687:Myh11
|
APN |
16 |
14,030,482 (GRCm39) |
nonsense |
probably null |
|
IGL02987:Myh11
|
APN |
16 |
14,050,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03008:Myh11
|
APN |
16 |
14,022,617 (GRCm39) |
missense |
probably benign |
0.00 |
G5030:Myh11
|
UTSW |
16 |
14,068,443 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4618001:Myh11
|
UTSW |
16 |
14,018,930 (GRCm39) |
missense |
|
|
R0008:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0086:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Myh11
|
UTSW |
16 |
14,022,231 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0096:Myh11
|
UTSW |
16 |
14,022,231 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0207:Myh11
|
UTSW |
16 |
14,029,124 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0326:Myh11
|
UTSW |
16 |
14,036,744 (GRCm39) |
missense |
probably benign |
0.32 |
R0546:Myh11
|
UTSW |
16 |
14,023,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Myh11
|
UTSW |
16 |
14,041,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0715:Myh11
|
UTSW |
16 |
14,044,480 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0839:Myh11
|
UTSW |
16 |
14,021,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R1014:Myh11
|
UTSW |
16 |
14,054,274 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1104:Myh11
|
UTSW |
16 |
14,019,991 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1426:Myh11
|
UTSW |
16 |
14,023,795 (GRCm39) |
nonsense |
probably null |
|
R1560:Myh11
|
UTSW |
16 |
14,044,484 (GRCm39) |
nonsense |
probably null |
|
R1714:Myh11
|
UTSW |
16 |
14,054,232 (GRCm39) |
critical splice donor site |
probably null |
|
R1742:Myh11
|
UTSW |
16 |
14,037,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Myh11
|
UTSW |
16 |
14,033,654 (GRCm39) |
missense |
probably damaging |
0.98 |
R1750:Myh11
|
UTSW |
16 |
14,018,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1753:Myh11
|
UTSW |
16 |
14,095,734 (GRCm39) |
missense |
probably benign |
|
R1760:Myh11
|
UTSW |
16 |
14,051,559 (GRCm39) |
splice site |
probably benign |
|
R1829:Myh11
|
UTSW |
16 |
14,041,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R1876:Myh11
|
UTSW |
16 |
14,086,967 (GRCm39) |
splice site |
probably benign |
|
R2027:Myh11
|
UTSW |
16 |
14,050,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Myh11
|
UTSW |
16 |
14,035,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Myh11
|
UTSW |
16 |
14,095,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2495:Myh11
|
UTSW |
16 |
14,023,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R2863:Myh11
|
UTSW |
16 |
14,057,290 (GRCm39) |
missense |
probably benign |
0.02 |
R3684:Myh11
|
UTSW |
16 |
14,021,098 (GRCm39) |
missense |
probably benign |
0.00 |
R3693:Myh11
|
UTSW |
16 |
14,035,813 (GRCm39) |
missense |
probably benign |
0.01 |
R4080:Myh11
|
UTSW |
16 |
14,041,923 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4367:Myh11
|
UTSW |
16 |
14,036,747 (GRCm39) |
missense |
probably damaging |
0.97 |
R4664:Myh11
|
UTSW |
16 |
14,044,448 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4673:Myh11
|
UTSW |
16 |
14,087,105 (GRCm39) |
missense |
probably damaging |
0.99 |
R4694:Myh11
|
UTSW |
16 |
14,018,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Myh11
|
UTSW |
16 |
14,052,329 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4806:Myh11
|
UTSW |
16 |
14,018,947 (GRCm39) |
splice site |
probably null |
|
R4905:Myh11
|
UTSW |
16 |
14,068,387 (GRCm39) |
missense |
probably benign |
0.13 |
R4939:Myh11
|
UTSW |
16 |
14,057,371 (GRCm39) |
missense |
probably benign |
|
R4964:Myh11
|
UTSW |
16 |
14,023,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4966:Myh11
|
UTSW |
16 |
14,023,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R5029:Myh11
|
UTSW |
16 |
14,023,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5045:Myh11
|
UTSW |
16 |
14,057,391 (GRCm39) |
nonsense |
probably null |
|
R5097:Myh11
|
UTSW |
16 |
14,023,770 (GRCm39) |
splice site |
probably null |
|
R5288:Myh11
|
UTSW |
16 |
14,025,872 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5385:Myh11
|
UTSW |
16 |
14,025,872 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5621:Myh11
|
UTSW |
16 |
14,062,719 (GRCm39) |
missense |
probably damaging |
0.96 |
R5856:Myh11
|
UTSW |
16 |
14,023,840 (GRCm39) |
missense |
probably benign |
0.00 |
R5869:Myh11
|
UTSW |
16 |
14,048,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Myh11
|
UTSW |
16 |
14,023,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6024:Myh11
|
UTSW |
16 |
14,095,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R6139:Myh11
|
UTSW |
16 |
14,033,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6209:Myh11
|
UTSW |
16 |
14,026,155 (GRCm39) |
nonsense |
probably null |
|
R6373:Myh11
|
UTSW |
16 |
14,022,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6671:Myh11
|
UTSW |
16 |
14,044,480 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6688:Myh11
|
UTSW |
16 |
14,023,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R6709:Myh11
|
UTSW |
16 |
14,041,358 (GRCm39) |
critical splice donor site |
probably null |
|
R7069:Myh11
|
UTSW |
16 |
14,036,803 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7176:Myh11
|
UTSW |
16 |
14,033,690 (GRCm39) |
missense |
|
|
R7644:Myh11
|
UTSW |
16 |
14,039,688 (GRCm39) |
missense |
|
|
R7838:Myh11
|
UTSW |
16 |
14,027,481 (GRCm39) |
missense |
|
|
R7905:Myh11
|
UTSW |
16 |
14,025,545 (GRCm39) |
nonsense |
probably null |
|
R8261:Myh11
|
UTSW |
16 |
14,041,867 (GRCm39) |
missense |
|
|
R8272:Myh11
|
UTSW |
16 |
14,036,718 (GRCm39) |
missense |
|
|
R8317:Myh11
|
UTSW |
16 |
14,025,941 (GRCm39) |
missense |
|
|
R8359:Myh11
|
UTSW |
16 |
14,026,095 (GRCm39) |
critical splice donor site |
probably null |
|
R8486:Myh11
|
UTSW |
16 |
14,022,532 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8527:Myh11
|
UTSW |
16 |
14,048,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R8861:Myh11
|
UTSW |
16 |
14,064,646 (GRCm39) |
missense |
|
|
R8886:Myh11
|
UTSW |
16 |
14,052,278 (GRCm39) |
missense |
|
|
R8946:Myh11
|
UTSW |
16 |
14,048,580 (GRCm39) |
missense |
probably benign |
0.08 |
R9151:Myh11
|
UTSW |
16 |
14,050,439 (GRCm39) |
missense |
|
|
R9253:Myh11
|
UTSW |
16 |
14,074,359 (GRCm39) |
missense |
|
|
R9257:Myh11
|
UTSW |
16 |
14,087,120 (GRCm39) |
missense |
|
|
R9273:Myh11
|
UTSW |
16 |
14,054,283 (GRCm39) |
missense |
|
|
R9320:Myh11
|
UTSW |
16 |
14,029,152 (GRCm39) |
missense |
|
|
R9364:Myh11
|
UTSW |
16 |
14,018,580 (GRCm39) |
missense |
|
|
R9365:Myh11
|
UTSW |
16 |
14,052,297 (GRCm39) |
missense |
|
|
R9496:Myh11
|
UTSW |
16 |
14,048,616 (GRCm39) |
nonsense |
probably null |
|
R9499:Myh11
|
UTSW |
16 |
14,064,673 (GRCm39) |
missense |
|
|
R9551:Myh11
|
UTSW |
16 |
14,064,673 (GRCm39) |
missense |
|
|
R9554:Myh11
|
UTSW |
16 |
14,018,580 (GRCm39) |
missense |
|
|
R9631:Myh11
|
UTSW |
16 |
14,025,441 (GRCm39) |
missense |
|
|
R9661:Myh11
|
UTSW |
16 |
14,041,857 (GRCm39) |
missense |
|
|
R9679:Myh11
|
UTSW |
16 |
14,095,436 (GRCm39) |
missense |
|
|
R9780:Myh11
|
UTSW |
16 |
14,064,613 (GRCm39) |
missense |
|
|
R9790:Myh11
|
UTSW |
16 |
14,025,992 (GRCm39) |
missense |
|
|
R9791:Myh11
|
UTSW |
16 |
14,025,992 (GRCm39) |
missense |
|
|
X0018:Myh11
|
UTSW |
16 |
14,095,497 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Myh11
|
UTSW |
16 |
14,027,553 (GRCm39) |
missense |
possibly damaging |
0.93 |
X0027:Myh11
|
UTSW |
16 |
14,052,266 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Myh11
|
UTSW |
16 |
14,087,126 (GRCm39) |
frame shift |
probably null |
|
Z1176:Myh11
|
UTSW |
16 |
14,095,639 (GRCm39) |
missense |
|
|
Z1176:Myh11
|
UTSW |
16 |
14,057,260 (GRCm39) |
missense |
probably null |
|
Z1177:Myh11
|
UTSW |
16 |
14,027,459 (GRCm39) |
missense |
|
|
|