Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
G |
A |
10: 87,042,061 (GRCm39) |
|
probably null |
Het |
4930522H14Rik |
G |
A |
4: 109,362,776 (GRCm39) |
A181V |
probably damaging |
Het |
Alk |
A |
T |
17: 72,274,549 (GRCm39) |
H587Q |
possibly damaging |
Het |
Ascc3 |
A |
G |
10: 50,604,393 (GRCm39) |
Y1371C |
probably benign |
Het |
Asxl1 |
T |
C |
2: 153,238,733 (GRCm39) |
F354S |
probably damaging |
Het |
Cachd1 |
A |
T |
4: 100,824,211 (GRCm39) |
I551F |
possibly damaging |
Het |
Cacna1e |
T |
C |
1: 154,347,149 (GRCm39) |
E1068G |
probably benign |
Het |
Cdc27 |
A |
T |
11: 104,403,830 (GRCm39) |
M644K |
probably damaging |
Het |
Chl1 |
T |
C |
6: 103,668,635 (GRCm39) |
V456A |
probably benign |
Het |
Ctxn1 |
A |
G |
8: 4,308,461 (GRCm39) |
Y57H |
probably damaging |
Het |
Cyp2c54 |
A |
G |
19: 40,058,688 (GRCm39) |
I248T |
probably benign |
Het |
Dchs2 |
A |
G |
3: 83,211,834 (GRCm39) |
T1878A |
probably benign |
Het |
Ddi2 |
A |
G |
4: 141,412,561 (GRCm39) |
V117A |
probably benign |
Het |
Dennd5a |
G |
T |
7: 109,533,196 (GRCm39) |
F191L |
probably benign |
Het |
Dnm3 |
C |
T |
1: 161,819,619 (GRCm39) |
R851H |
possibly damaging |
Het |
Eif3l |
G |
A |
15: 78,973,799 (GRCm39) |
D405N |
possibly damaging |
Het |
Espn |
T |
A |
4: 152,215,738 (GRCm39) |
D507V |
possibly damaging |
Het |
Fam83f |
A |
T |
15: 80,576,704 (GRCm39) |
S452C |
possibly damaging |
Het |
Fbxo22 |
A |
C |
9: 55,125,651 (GRCm39) |
E171D |
probably damaging |
Het |
Fgl2 |
T |
C |
5: 21,577,752 (GRCm39) |
V13A |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,807,044 (GRCm39) |
H1121R |
probably benign |
Het |
G0s2 |
A |
T |
1: 192,955,081 (GRCm39) |
M1K |
probably null |
Het |
Gnptab |
G |
A |
10: 88,276,254 (GRCm39) |
|
probably null |
Het |
Grm1 |
G |
A |
10: 10,956,096 (GRCm39) |
P63S |
probably benign |
Het |
Grsf1 |
G |
A |
5: 88,823,523 (GRCm39) |
|
probably benign |
Het |
Hcfc1r1 |
G |
A |
17: 23,892,985 (GRCm39) |
G10D |
probably damaging |
Het |
Hdac1-ps |
A |
C |
17: 78,799,447 (GRCm39) |
E146A |
probably damaging |
Het |
Igsf11 |
T |
C |
16: 38,827,565 (GRCm39) |
V41A |
possibly damaging |
Het |
Il17a |
C |
A |
1: 20,802,351 (GRCm39) |
A20E |
probably benign |
Het |
Kcnv2 |
A |
G |
19: 27,300,332 (GRCm39) |
Y61C |
probably damaging |
Het |
Kmt2c |
A |
G |
5: 25,499,697 (GRCm39) |
M481T |
possibly damaging |
Het |
Krt40 |
A |
T |
11: 99,430,961 (GRCm39) |
C263S |
possibly damaging |
Het |
Larp1 |
T |
C |
11: 57,938,540 (GRCm39) |
V441A |
possibly damaging |
Het |
Lrwd1 |
T |
C |
5: 136,160,983 (GRCm39) |
E300G |
probably damaging |
Het |
Mcoln3 |
G |
T |
3: 145,845,230 (GRCm39) |
W475C |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,058,796 (GRCm39) |
I30T |
probably benign |
Het |
Mmd |
T |
A |
11: 90,158,433 (GRCm39) |
V181D |
probably benign |
Het |
Muc4 |
T |
A |
16: 32,752,558 (GRCm38) |
L812* |
probably null |
Het |
Mycbp2 |
T |
C |
14: 103,414,729 (GRCm39) |
D2561G |
probably benign |
Het |
Myl12a |
G |
T |
17: 71,303,166 (GRCm39) |
N95K |
probably benign |
Het |
Myo1h |
A |
G |
5: 114,466,872 (GRCm39) |
|
probably null |
Het |
Myrf |
G |
A |
19: 10,196,983 (GRCm39) |
P266S |
possibly damaging |
Het |
Ncf1 |
A |
G |
5: 134,250,949 (GRCm39) |
V330A |
possibly damaging |
Het |
Nfasc |
T |
C |
1: 132,533,287 (GRCm39) |
D638G |
probably damaging |
Het |
Nkapl |
T |
C |
13: 21,651,437 (GRCm39) |
K392R |
possibly damaging |
Het |
Or2y3 |
A |
G |
17: 38,393,293 (GRCm39) |
V192A |
probably benign |
Het |
Or6a2 |
A |
T |
7: 106,600,514 (GRCm39) |
C184* |
probably null |
Het |
Or8b50 |
A |
G |
9: 38,517,708 (GRCm39) |
|
probably benign |
Het |
Pelo |
T |
A |
13: 115,226,184 (GRCm39) |
N91I |
probably damaging |
Het |
Ptk2b |
T |
C |
14: 66,395,850 (GRCm39) |
N836D |
probably benign |
Het |
Pwp2 |
A |
T |
10: 78,018,778 (GRCm39) |
|
probably null |
Het |
Slc44a1 |
G |
A |
4: 53,517,657 (GRCm39) |
V127I |
probably benign |
Het |
Snx13 |
A |
G |
12: 35,155,174 (GRCm39) |
T413A |
probably benign |
Het |
Spaca7 |
C |
T |
8: 12,635,696 (GRCm39) |
P71S |
probably damaging |
Het |
Spef2 |
A |
T |
15: 9,609,637 (GRCm39) |
M1296K |
possibly damaging |
Het |
Suco |
G |
A |
1: 161,656,890 (GRCm39) |
A978V |
probably benign |
Het |
Tcerg1 |
A |
G |
18: 42,670,002 (GRCm39) |
E494G |
probably benign |
Het |
Tenm2 |
A |
G |
11: 35,997,626 (GRCm39) |
V821A |
probably benign |
Het |
Tg |
T |
A |
15: 66,565,112 (GRCm39) |
D1151E |
probably benign |
Het |
Trp53bp2 |
A |
G |
1: 182,283,384 (GRCm39) |
E1040G |
probably damaging |
Het |
Ubap2 |
A |
T |
4: 41,233,655 (GRCm39) |
N79K |
probably damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Yars2 |
T |
G |
16: 16,122,385 (GRCm39) |
|
probably null |
Het |
Ylpm1 |
A |
G |
12: 85,095,640 (GRCm39) |
I1847V |
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 |
|
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 |
|
|
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 |
|
|
|