Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl1 |
T |
A |
8: 46,961,374 (GRCm39) |
N106K |
probably damaging |
Het |
Ak8 |
T |
C |
2: 28,632,767 (GRCm39) |
|
probably benign |
Het |
BC016579 |
C |
T |
16: 45,449,849 (GRCm39) |
G190S |
probably damaging |
Het |
C4bp |
A |
G |
1: 130,564,454 (GRCm39) |
V410A |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,780,388 (GRCm39) |
T658A |
probably damaging |
Het |
Cadps2 |
T |
C |
6: 23,287,659 (GRCm39) |
|
probably null |
Het |
Car10 |
G |
T |
11: 93,381,351 (GRCm39) |
V105F |
probably damaging |
Het |
Car15 |
C |
T |
16: 17,653,249 (GRCm39) |
C306Y |
possibly damaging |
Het |
Casr |
C |
T |
16: 36,316,250 (GRCm39) |
A530T |
probably benign |
Het |
Col5a3 |
A |
G |
9: 20,708,868 (GRCm39) |
|
probably null |
Het |
Creld1 |
A |
G |
6: 113,465,058 (GRCm39) |
E95G |
probably damaging |
Het |
Dcstamp |
T |
A |
15: 39,623,793 (GRCm39) |
D366E |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 117,866,856 (GRCm39) |
Y4095C |
probably damaging |
Het |
Eps8l2 |
A |
G |
7: 140,937,148 (GRCm39) |
|
probably benign |
Het |
Gsn |
T |
C |
2: 35,172,471 (GRCm39) |
|
probably benign |
Het |
Ifi27l2a |
T |
C |
12: 103,401,803 (GRCm39) |
V30A |
possibly damaging |
Het |
Ifit1bl2 |
C |
T |
19: 34,597,124 (GRCm39) |
R164Q |
probably benign |
Het |
Impg2 |
T |
C |
16: 56,088,779 (GRCm39) |
S1102P |
probably damaging |
Het |
Kif24 |
G |
T |
4: 41,394,323 (GRCm39) |
P984Q |
possibly damaging |
Het |
Krtap29-1 |
T |
A |
11: 99,869,455 (GRCm39) |
Q142L |
possibly damaging |
Het |
Lpar6 |
C |
T |
14: 73,476,510 (GRCm39) |
T157I |
probably benign |
Het |
Lrrc32 |
A |
T |
7: 98,148,629 (GRCm39) |
T470S |
probably benign |
Het |
Lyl1 |
C |
T |
8: 85,429,300 (GRCm39) |
P3L |
possibly damaging |
Het |
Mroh9 |
A |
T |
1: 162,854,071 (GRCm39) |
H776Q |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,462,031 (GRCm39) |
N309S |
possibly damaging |
Het |
Myo5b |
A |
T |
18: 74,767,630 (GRCm39) |
T313S |
probably benign |
Het |
Myo5b |
G |
A |
18: 74,713,615 (GRCm39) |
|
probably benign |
Het |
Npas4 |
C |
T |
19: 5,036,365 (GRCm39) |
V600M |
probably damaging |
Het |
Nrxn3 |
T |
A |
12: 89,478,698 (GRCm39) |
Y557* |
probably null |
Het |
Or2aj4 |
T |
C |
16: 19,385,463 (GRCm39) |
T57A |
possibly damaging |
Het |
Or52k2 |
A |
G |
7: 102,253,946 (GRCm39) |
I128M |
probably damaging |
Het |
Or8g53 |
T |
A |
9: 39,683,458 (GRCm39) |
T213S |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,152,843 (GRCm39) |
I383V |
probably damaging |
Het |
Pdzrn3 |
C |
A |
6: 101,128,816 (GRCm39) |
D617Y |
probably damaging |
Het |
Prodh2 |
A |
T |
7: 30,212,258 (GRCm39) |
K408* |
probably null |
Het |
Ptprs |
T |
C |
17: 56,725,830 (GRCm39) |
I1052V |
probably damaging |
Het |
Rpl14 |
T |
C |
9: 120,401,193 (GRCm39) |
V12A |
probably damaging |
Het |
Sf3a1 |
C |
T |
11: 4,125,493 (GRCm39) |
R428C |
probably damaging |
Het |
Sgsm2 |
G |
T |
11: 74,741,962 (GRCm39) |
N1009K |
probably damaging |
Het |
Slc28a2 |
A |
T |
2: 122,284,980 (GRCm39) |
I323F |
probably damaging |
Het |
Snx19 |
T |
A |
9: 30,344,928 (GRCm39) |
F676I |
probably damaging |
Het |
Stxbp2 |
A |
T |
8: 3,691,971 (GRCm39) |
I538F |
probably benign |
Het |
Tg |
A |
C |
15: 66,543,254 (GRCm39) |
D56A |
probably damaging |
Het |
Tln1 |
G |
T |
4: 43,545,694 (GRCm39) |
A928E |
probably damaging |
Het |
Tmem94 |
T |
C |
11: 115,683,247 (GRCm39) |
S677P |
possibly damaging |
Het |
Ttc41 |
C |
A |
10: 86,572,721 (GRCm39) |
H698N |
possibly damaging |
Het |
Vcan |
T |
C |
13: 89,851,394 (GRCm39) |
T1189A |
probably benign |
Het |
Vmn1r215 |
G |
T |
13: 23,260,088 (GRCm39) |
V43F |
probably damaging |
Het |
Vmn2r28 |
A |
T |
7: 5,487,015 (GRCm39) |
N549K |
probably damaging |
Het |
Zfp598 |
T |
C |
17: 24,898,566 (GRCm39) |
V455A |
probably benign |
Het |
|
Other mutations in Myh7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Myh7
|
APN |
14 |
55,224,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01025:Myh7
|
APN |
14 |
55,216,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01092:Myh7
|
APN |
14 |
55,209,089 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01384:Myh7
|
APN |
14 |
55,208,916 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh7
|
APN |
14 |
55,226,336 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01671:Myh7
|
APN |
14 |
55,210,381 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01923:Myh7
|
APN |
14 |
55,222,916 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02183:Myh7
|
APN |
14 |
55,212,188 (GRCm39) |
missense |
probably benign |
|
IGL02379:Myh7
|
APN |
14 |
55,216,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02884:Myh7
|
APN |
14 |
55,230,276 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02898:Myh7
|
APN |
14 |
55,221,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Myh7
|
APN |
14 |
55,221,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03145:Myh7
|
APN |
14 |
55,220,802 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03250:Myh7
|
APN |
14 |
55,229,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03394:Myh7
|
APN |
14 |
55,212,818 (GRCm39) |
missense |
probably damaging |
1.00 |
BB008:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB018:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0019:Myh7
|
UTSW |
14 |
55,221,191 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0030:Myh7
|
UTSW |
14 |
55,229,427 (GRCm39) |
missense |
probably benign |
0.00 |
R0183:Myh7
|
UTSW |
14 |
55,216,333 (GRCm39) |
missense |
probably benign |
0.02 |
R0230:Myh7
|
UTSW |
14 |
55,211,390 (GRCm39) |
missense |
probably benign |
0.03 |
R0295:Myh7
|
UTSW |
14 |
55,222,278 (GRCm39) |
splice site |
probably benign |
|
R0423:Myh7
|
UTSW |
14 |
55,216,646 (GRCm39) |
missense |
probably benign |
0.06 |
R0537:Myh7
|
UTSW |
14 |
55,228,256 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0541:Myh7
|
UTSW |
14 |
55,212,158 (GRCm39) |
missense |
probably benign |
|
R0581:Myh7
|
UTSW |
14 |
55,222,953 (GRCm39) |
missense |
probably benign |
0.02 |
R0786:Myh7
|
UTSW |
14 |
55,230,330 (GRCm39) |
start codon destroyed |
probably null |
|
R0866:Myh7
|
UTSW |
14 |
55,210,596 (GRCm39) |
missense |
probably benign |
|
R1068:Myh7
|
UTSW |
14 |
55,224,776 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1075:Myh7
|
UTSW |
14 |
55,224,860 (GRCm39) |
missense |
probably benign |
|
R1124:Myh7
|
UTSW |
14 |
55,211,327 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1140:Myh7
|
UTSW |
14 |
55,210,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Myh7
|
UTSW |
14 |
55,225,908 (GRCm39) |
missense |
probably benign |
0.00 |
R1653:Myh7
|
UTSW |
14 |
55,228,246 (GRCm39) |
missense |
probably benign |
0.00 |
R1677:Myh7
|
UTSW |
14 |
55,224,973 (GRCm39) |
missense |
probably benign |
0.17 |
R1760:Myh7
|
UTSW |
14 |
55,210,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R1838:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1839:Myh7
|
UTSW |
14 |
55,210,637 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2483:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R2566:Myh7
|
UTSW |
14 |
55,220,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R3623:Myh7
|
UTSW |
14 |
55,210,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R3916:Myh7
|
UTSW |
14 |
55,211,503 (GRCm39) |
missense |
probably damaging |
0.97 |
R4236:Myh7
|
UTSW |
14 |
55,228,575 (GRCm39) |
missense |
probably benign |
0.34 |
R4471:Myh7
|
UTSW |
14 |
55,229,311 (GRCm39) |
nonsense |
probably null |
|
R4700:Myh7
|
UTSW |
14 |
55,225,778 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4805:Myh7
|
UTSW |
14 |
55,222,590 (GRCm39) |
missense |
probably benign |
0.27 |
R4880:Myh7
|
UTSW |
14 |
55,216,045 (GRCm39) |
missense |
probably benign |
0.18 |
R4975:Myh7
|
UTSW |
14 |
55,209,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Myh7
|
UTSW |
14 |
55,210,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R5004:Myh7
|
UTSW |
14 |
55,209,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R5107:Myh7
|
UTSW |
14 |
55,223,881 (GRCm39) |
intron |
probably benign |
|
R5124:Myh7
|
UTSW |
14 |
55,223,199 (GRCm39) |
nonsense |
probably null |
|
R5256:Myh7
|
UTSW |
14 |
55,216,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Myh7
|
UTSW |
14 |
55,224,020 (GRCm39) |
intron |
probably benign |
|
R5581:Myh7
|
UTSW |
14 |
55,216,411 (GRCm39) |
missense |
probably benign |
0.00 |
R5861:Myh7
|
UTSW |
14 |
55,226,347 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5957:Myh7
|
UTSW |
14 |
55,226,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Myh7
|
UTSW |
14 |
55,208,259 (GRCm39) |
missense |
probably benign |
0.01 |
R6184:Myh7
|
UTSW |
14 |
55,226,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Myh7
|
UTSW |
14 |
55,226,753 (GRCm39) |
missense |
probably benign |
0.00 |
R6268:Myh7
|
UTSW |
14 |
55,226,741 (GRCm39) |
missense |
probably benign |
0.00 |
R6274:Myh7
|
UTSW |
14 |
55,216,943 (GRCm39) |
missense |
probably damaging |
0.97 |
R6345:Myh7
|
UTSW |
14 |
55,221,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Myh7
|
UTSW |
14 |
55,226,351 (GRCm39) |
missense |
probably benign |
0.00 |
R6641:Myh7
|
UTSW |
14 |
55,219,737 (GRCm39) |
missense |
probably benign |
0.37 |
R6755:Myh7
|
UTSW |
14 |
55,229,770 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6952:Myh7
|
UTSW |
14 |
55,229,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Myh7
|
UTSW |
14 |
55,212,101 (GRCm39) |
nonsense |
probably null |
|
R7201:Myh7
|
UTSW |
14 |
55,228,402 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7257:Myh7
|
UTSW |
14 |
55,209,947 (GRCm39) |
splice site |
probably null |
|
R7296:Myh7
|
UTSW |
14 |
55,227,482 (GRCm39) |
missense |
probably benign |
0.05 |
R7709:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7710:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7711:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Myh7
|
UTSW |
14 |
55,227,500 (GRCm39) |
missense |
probably benign |
0.09 |
R7869:Myh7
|
UTSW |
14 |
55,226,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Myh7
|
UTSW |
14 |
55,226,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R7887:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7931:Myh7
|
UTSW |
14 |
55,221,119 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7936:Myh7
|
UTSW |
14 |
55,216,920 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8056:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8061:Myh7
|
UTSW |
14 |
55,228,398 (GRCm39) |
missense |
probably benign |
|
R8101:Myh7
|
UTSW |
14 |
55,210,776 (GRCm39) |
nonsense |
probably null |
|
R8202:Myh7
|
UTSW |
14 |
55,227,497 (GRCm39) |
missense |
probably benign |
|
R8504:Myh7
|
UTSW |
14 |
55,227,786 (GRCm39) |
missense |
probably damaging |
0.98 |
R8560:Myh7
|
UTSW |
14 |
55,213,405 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8843:Myh7
|
UTSW |
14 |
55,212,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R8903:Myh7
|
UTSW |
14 |
55,230,228 (GRCm39) |
nonsense |
probably null |
|
R8926:Myh7
|
UTSW |
14 |
55,222,533 (GRCm39) |
missense |
probably benign |
0.33 |
R8936:Myh7
|
UTSW |
14 |
55,228,440 (GRCm39) |
missense |
probably benign |
0.00 |
R9182:Myh7
|
UTSW |
14 |
55,226,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R9260:Myh7
|
UTSW |
14 |
55,224,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R9264:Myh7
|
UTSW |
14 |
55,213,454 (GRCm39) |
missense |
probably benign |
0.01 |
R9288:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.35 |
R9362:Myh7
|
UTSW |
14 |
55,222,932 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Myh7
|
UTSW |
14 |
55,217,841 (GRCm39) |
missense |
probably benign |
0.12 |
R9561:Myh7
|
UTSW |
14 |
55,216,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9663:Myh7
|
UTSW |
14 |
55,221,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R9789:Myh7
|
UTSW |
14 |
55,229,384 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1192:Myh7
|
UTSW |
14 |
55,220,748 (GRCm39) |
missense |
probably damaging |
0.99 |
|