Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam32 |
T |
C |
8: 25,374,471 (GRCm39) |
E507G |
probably damaging |
Het |
Adam39 |
C |
T |
8: 41,277,768 (GRCm39) |
T53I |
probably benign |
Het |
Adam4 |
A |
T |
12: 81,468,535 (GRCm39) |
S29T |
possibly damaging |
Het |
Adamdec1 |
C |
A |
14: 68,815,353 (GRCm39) |
E104* |
probably null |
Het |
Alas1 |
G |
T |
9: 106,113,676 (GRCm39) |
P523Q |
probably damaging |
Het |
Aldh3a1 |
A |
G |
11: 61,104,320 (GRCm39) |
D69G |
probably benign |
Het |
Arhgap29 |
T |
A |
3: 121,808,620 (GRCm39) |
V1266E |
probably damaging |
Het |
Bcdin3d |
T |
C |
15: 99,368,719 (GRCm39) |
D160G |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,955,772 (GRCm39) |
F569I |
probably benign |
Het |
Cacna1b |
A |
G |
2: 24,521,956 (GRCm39) |
L1718S |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,629,975 (GRCm39) |
Y457C |
probably damaging |
Het |
Creb3 |
T |
C |
4: 43,563,192 (GRCm39) |
V97A |
probably benign |
Het |
Cux2 |
G |
T |
5: 122,025,539 (GRCm39) |
S43* |
probably null |
Het |
Fhip1a |
A |
T |
3: 85,638,020 (GRCm39) |
V93D |
probably damaging |
Het |
Fsbp |
T |
G |
4: 11,579,841 (GRCm39) |
N36K |
probably benign |
Het |
Gm11565 |
A |
G |
11: 99,806,040 (GRCm39) |
D144G |
probably benign |
Het |
Gpn3 |
A |
G |
5: 122,511,981 (GRCm39) |
Y19C |
probably damaging |
Het |
Gstz1 |
A |
T |
12: 87,208,837 (GRCm39) |
T148S |
probably benign |
Het |
Gtf3c5 |
A |
G |
2: 28,462,236 (GRCm39) |
I282T |
probably benign |
Het |
Hspa2 |
T |
A |
12: 76,452,514 (GRCm39) |
S403T |
possibly damaging |
Het |
Il27 |
G |
A |
7: 126,190,251 (GRCm39) |
T121I |
possibly damaging |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kctd1 |
T |
A |
18: 15,196,284 (GRCm39) |
|
probably benign |
Het |
Kynu |
A |
G |
2: 43,569,815 (GRCm39) |
T366A |
probably damaging |
Het |
Lama5 |
G |
A |
2: 179,841,059 (GRCm39) |
T507I |
probably damaging |
Het |
Myh14 |
T |
A |
7: 44,273,754 (GRCm39) |
H1331L |
probably damaging |
Het |
Myh2 |
T |
A |
11: 67,079,303 (GRCm39) |
L957Q |
probably damaging |
Het |
Myh4 |
T |
C |
11: 67,137,227 (GRCm39) |
F483L |
probably benign |
Het |
Nbeal1 |
A |
C |
1: 60,368,549 (GRCm39) |
K2631N |
probably damaging |
Het |
Ofcc1 |
G |
A |
13: 40,168,864 (GRCm39) |
T841I |
probably damaging |
Het |
Ogg1 |
T |
C |
6: 113,304,268 (GRCm39) |
C28R |
probably damaging |
Het |
Or13c7c |
T |
C |
4: 43,836,430 (GRCm39) |
H20R |
probably benign |
Het |
Or5b24 |
G |
A |
19: 12,912,461 (GRCm39) |
A120T |
probably damaging |
Het |
Or5k17 |
C |
T |
16: 58,746,053 (GRCm39) |
V294I |
possibly damaging |
Het |
Or6e1 |
C |
T |
14: 54,519,789 (GRCm39) |
A188T |
possibly damaging |
Het |
Or7g35 |
A |
G |
9: 19,496,726 (GRCm39) |
K298E |
possibly damaging |
Het |
Parp6 |
G |
C |
9: 59,547,393 (GRCm39) |
R460P |
probably damaging |
Het |
Phf14 |
A |
G |
6: 11,992,056 (GRCm39) |
H744R |
probably damaging |
Het |
Pibf1 |
A |
G |
14: 99,370,787 (GRCm39) |
N263S |
possibly damaging |
Het |
Plcb4 |
A |
G |
2: 135,774,191 (GRCm39) |
T158A |
possibly damaging |
Het |
Plce1 |
T |
C |
19: 38,737,840 (GRCm39) |
S1615P |
possibly damaging |
Het |
Plxna3 |
T |
G |
X: 73,382,554 (GRCm39) |
|
probably null |
Het |
Rad54b |
T |
A |
4: 11,609,449 (GRCm39) |
H633Q |
probably benign |
Het |
Rgs22 |
T |
A |
15: 36,100,079 (GRCm39) |
Y212F |
probably benign |
Het |
Rnd3 |
G |
A |
2: 51,022,553 (GRCm39) |
A163V |
probably benign |
Het |
Rnf10 |
A |
T |
5: 115,389,148 (GRCm39) |
V315E |
probably damaging |
Het |
Robo2 |
C |
T |
16: 73,701,266 (GRCm39) |
|
probably null |
Het |
Rp1l1 |
T |
G |
14: 64,268,719 (GRCm39) |
V1435G |
probably damaging |
Het |
Scaf8 |
T |
A |
17: 3,248,260 (GRCm39) |
D1194E |
probably benign |
Het |
Septin12 |
T |
C |
16: 4,809,807 (GRCm39) |
T198A |
probably damaging |
Het |
Shisa2 |
A |
G |
14: 59,867,629 (GRCm39) |
T294A |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,018,628 (GRCm39) |
|
probably null |
Het |
Strbp |
A |
T |
2: 37,535,691 (GRCm39) |
S6T |
probably damaging |
Het |
Syf2 |
A |
G |
4: 134,661,804 (GRCm39) |
E56G |
probably damaging |
Het |
Thap4 |
T |
C |
1: 93,642,588 (GRCm39) |
|
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 18,887,580 (GRCm39) |
|
probably benign |
Het |
Tnxb |
A |
G |
17: 34,891,514 (GRCm39) |
E619G |
probably damaging |
Het |
Tpr |
G |
A |
1: 150,299,318 (GRCm39) |
A1173T |
probably benign |
Het |
Tspan3 |
G |
A |
9: 56,043,980 (GRCm39) |
R240W |
probably damaging |
Het |
Tut7 |
G |
T |
13: 59,944,659 (GRCm39) |
T658K |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,138,027 (GRCm39) |
S1128L |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,021,876 (GRCm39) |
V236A |
probably damaging |
Het |
Usp34 |
TCACCACCACCACCACCACCACCACCAC |
TCACCACCACCACCACCACCACCAC |
11: 23,314,480 (GRCm39) |
|
probably benign |
Het |
Zfp940 |
T |
C |
7: 29,544,863 (GRCm39) |
D348G |
probably benign |
Het |
Zpld2 |
G |
A |
4: 133,927,658 (GRCm39) |
A365V |
probably benign |
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 |
R0085: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 |
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 |
|
|
|