Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
A |
T |
10: 100,448,680 (GRCm39) |
|
probably null |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
Abcc5 |
A |
G |
16: 20,218,678 (GRCm39) |
S235P |
probably damaging |
Het |
Abcc6 |
T |
C |
7: 45,644,649 (GRCm39) |
N842S |
probably benign |
Het |
Acbd6 |
G |
A |
1: 155,500,669 (GRCm39) |
V210I |
probably benign |
Het |
Ahctf1 |
A |
T |
1: 179,576,192 (GRCm39) |
V2130D |
probably damaging |
Het |
Akap5 |
A |
G |
12: 76,375,207 (GRCm39) |
E213G |
probably damaging |
Het |
Alyref |
T |
G |
11: 120,486,879 (GRCm39) |
|
probably null |
Het |
Anapc5 |
G |
T |
5: 122,955,973 (GRCm39) |
N152K |
probably benign |
Het |
Atp8b2 |
A |
T |
3: 89,856,315 (GRCm39) |
D416E |
probably benign |
Het |
AW551984 |
A |
T |
9: 39,508,454 (GRCm39) |
V354E |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,364,162 (GRCm39) |
E844G |
probably damaging |
Het |
Bmp1 |
C |
T |
14: 70,728,802 (GRCm39) |
R590H |
probably benign |
Het |
Ccnh |
T |
C |
13: 85,354,254 (GRCm39) |
S233P |
possibly damaging |
Het |
Cdca7 |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGA |
TGAAGAAGAAGAAGAAGAAGAAGAAGAAGA |
2: 72,312,205 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
A |
G |
9: 105,644,623 (GRCm39) |
S1222P |
probably damaging |
Het |
Dhfr |
G |
A |
13: 92,502,282 (GRCm39) |
G118S |
probably damaging |
Het |
Dnah9 |
G |
A |
11: 65,764,950 (GRCm39) |
R1414* |
probably null |
Het |
Dnai1 |
A |
G |
4: 41,614,269 (GRCm39) |
D315G |
probably benign |
Het |
Eogt |
T |
C |
6: 97,119,792 (GRCm39) |
R139G |
probably benign |
Het |
Fcgbpl1 |
A |
T |
7: 27,856,408 (GRCm39) |
K2065M |
possibly damaging |
Het |
Fh1 |
C |
T |
1: 175,446,639 (GRCm39) |
G79E |
probably damaging |
Het |
Gabrg3 |
A |
G |
7: 56,374,304 (GRCm39) |
Y421H |
probably damaging |
Het |
Glipr1 |
C |
A |
10: 111,821,545 (GRCm39) |
R219L |
probably damaging |
Het |
Gm1123 |
T |
C |
9: 98,891,369 (GRCm39) |
D360G |
probably benign |
Het |
Ift81 |
C |
T |
5: 122,729,142 (GRCm39) |
|
probably null |
Het |
Itsn2 |
A |
G |
12: 4,684,583 (GRCm39) |
|
probably benign |
Het |
Kri1 |
A |
T |
9: 21,198,998 (GRCm39) |
H55Q |
probably benign |
Het |
Mcidas |
C |
T |
13: 113,134,038 (GRCm39) |
T174M |
possibly damaging |
Het |
Mcidas |
C |
A |
13: 113,130,951 (GRCm39) |
A92E |
possibly damaging |
Het |
Mmp25 |
C |
A |
17: 23,863,022 (GRCm39) |
G130* |
probably null |
Het |
Myo10 |
A |
G |
15: 25,800,298 (GRCm39) |
D1458G |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,139,104 (GRCm39) |
T154A |
probably damaging |
Het |
Nfatc4 |
T |
C |
14: 56,068,039 (GRCm39) |
I620T |
probably benign |
Het |
Nos3 |
A |
T |
5: 24,572,329 (GRCm39) |
Y134F |
probably benign |
Het |
Nup50l |
T |
A |
6: 96,142,911 (GRCm39) |
R44S |
possibly damaging |
Het |
Or13c3 |
T |
C |
4: 52,855,613 (GRCm39) |
N300S |
probably damaging |
Het |
Or51a6 |
A |
T |
7: 102,604,721 (GRCm39) |
I36N |
probably damaging |
Het |
Or5b106 |
C |
A |
19: 13,123,541 (GRCm39) |
A161S |
probably benign |
Het |
Or6c209 |
T |
A |
10: 129,483,792 (GRCm39) |
V265E |
possibly damaging |
Het |
Pax9 |
G |
T |
12: 56,743,411 (GRCm39) |
R19S |
probably damaging |
Het |
Pcdha9 |
T |
C |
18: 37,131,945 (GRCm39) |
I338T |
probably damaging |
Het |
Plxnb2 |
G |
T |
15: 89,041,614 (GRCm39) |
T1730K |
probably damaging |
Het |
Rac1 |
A |
G |
5: 143,502,907 (GRCm39) |
|
probably null |
Het |
Samsn1 |
G |
T |
16: 75,673,353 (GRCm39) |
F174L |
possibly damaging |
Het |
Scaf1 |
G |
A |
7: 44,662,129 (GRCm39) |
T86M |
probably damaging |
Het |
Smc1b |
A |
G |
15: 84,950,428 (GRCm39) |
Y1199H |
probably damaging |
Het |
Svep1 |
A |
G |
4: 58,069,308 (GRCm39) |
I2826T |
probably benign |
Het |
Tex36 |
A |
G |
7: 133,189,182 (GRCm39) |
V130A |
probably damaging |
Het |
Tigd5 |
A |
G |
15: 75,783,252 (GRCm39) |
H538R |
probably damaging |
Het |
Tlr3 |
C |
A |
8: 45,852,260 (GRCm39) |
|
probably null |
Het |
Tubb2b |
A |
T |
13: 34,312,187 (GRCm39) |
I202N |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,587,674 (GRCm39) |
V1453A |
probably benign |
Het |
Unc5c |
A |
T |
3: 141,507,071 (GRCm39) |
T608S |
probably benign |
Het |
Vrk1 |
C |
A |
12: 106,018,087 (GRCm39) |
H119N |
probably damaging |
Het |
Wdr53 |
T |
A |
16: 32,075,476 (GRCm39) |
M227K |
probably benign |
Het |
Xpo4 |
T |
C |
14: 57,875,746 (GRCm39) |
D129G |
possibly damaging |
Het |
Zcchc4 |
T |
C |
5: 52,953,992 (GRCm39) |
I224T |
probably damaging |
Het |
Zdhhc1 |
T |
A |
8: 106,210,326 (GRCm39) |
E30D |
probably damaging |
Het |
Zscan29 |
C |
G |
2: 120,991,864 (GRCm39) |
R540T |
possibly damaging |
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 |
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 |
|
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 |
|
|
|