Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap2 |
A |
G |
16: 30,920,641 (GRCm39) |
|
probably null |
Het |
Adgrb3 |
T |
C |
1: 25,865,496 (GRCm39) |
N116D |
probably benign |
Het |
Arfgef1 |
T |
A |
1: 10,243,122 (GRCm39) |
R1073* |
probably null |
Het |
Atp6v1d |
T |
A |
12: 78,904,023 (GRCm39) |
Q46L |
probably benign |
Het |
Brme1 |
A |
G |
8: 84,898,878 (GRCm39) |
S589G |
possibly damaging |
Het |
Car15 |
A |
T |
16: 17,653,246 (GRCm39) |
L307* |
probably null |
Het |
Catspere2 |
A |
T |
1: 177,938,996 (GRCm39) |
H623L |
possibly damaging |
Het |
Ccdc146 |
T |
C |
5: 21,502,023 (GRCm39) |
D797G |
probably damaging |
Het |
Ccdc27 |
A |
T |
4: 154,125,507 (GRCm39) |
D112E |
unknown |
Het |
Ccp110 |
A |
G |
7: 118,321,673 (GRCm39) |
I443V |
probably benign |
Het |
Cd74 |
T |
A |
18: 60,941,364 (GRCm39) |
M103K |
possibly damaging |
Het |
Cdca2 |
T |
A |
14: 67,914,831 (GRCm39) |
R809S |
possibly damaging |
Het |
Cfap46 |
A |
T |
7: 139,198,165 (GRCm39) |
V2061E |
unknown |
Het |
Cimap1b |
T |
C |
15: 89,262,601 (GRCm39) |
S119G |
probably benign |
Het |
Ddx11 |
G |
A |
17: 66,457,807 (GRCm39) |
E873K |
probably benign |
Het |
Gucy2d |
G |
A |
7: 98,116,979 (GRCm39) |
|
probably null |
Het |
Herc1 |
T |
A |
9: 66,309,834 (GRCm39) |
S1061R |
probably damaging |
Het |
Ildr1 |
G |
A |
16: 36,536,574 (GRCm39) |
R201H |
probably damaging |
Het |
Jakmip2 |
T |
A |
18: 43,715,194 (GRCm39) |
I111F |
possibly damaging |
Het |
Kcnj2 |
A |
G |
11: 110,963,355 (GRCm39) |
D249G |
probably damaging |
Het |
Kif1a |
T |
A |
1: 93,002,776 (GRCm39) |
T208S |
probably damaging |
Het |
Mgam |
T |
G |
6: 40,706,577 (GRCm39) |
M76R |
probably damaging |
Het |
Mib1 |
T |
G |
18: 10,800,088 (GRCm39) |
I809S |
probably benign |
Het |
Mzf1 |
T |
C |
7: 12,777,647 (GRCm39) |
T665A |
probably benign |
Het |
Nfya |
T |
C |
17: 48,699,943 (GRCm39) |
H27R |
|
Het |
Nhsl3 |
A |
G |
4: 129,117,269 (GRCm39) |
V510A |
probably benign |
Het |
Nktr |
T |
C |
9: 121,579,415 (GRCm39) |
M1161T |
unknown |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Or13c7b |
C |
T |
4: 43,821,109 (GRCm39) |
G84D |
probably benign |
Het |
Pde8b |
C |
T |
13: 95,169,424 (GRCm39) |
D567N |
probably damaging |
Het |
Pik3cd |
A |
G |
4: 149,740,087 (GRCm39) |
I491T |
possibly damaging |
Het |
Plcd3 |
G |
T |
11: 102,968,380 (GRCm39) |
Y392* |
probably null |
Het |
Plcd4 |
A |
G |
1: 74,588,359 (GRCm39) |
I69M |
probably damaging |
Het |
Plekhm2 |
T |
C |
4: 141,356,443 (GRCm39) |
Y799C |
probably damaging |
Het |
Pnlip |
T |
A |
19: 58,669,273 (GRCm39) |
I424N |
possibly damaging |
Het |
Prlr |
A |
G |
15: 10,326,550 (GRCm39) |
|
probably benign |
Het |
Ptprq |
A |
G |
10: 107,522,247 (GRCm39) |
V568A |
probably benign |
Het |
Rtkn |
A |
G |
6: 83,125,143 (GRCm39) |
E201G |
probably damaging |
Het |
Scg2 |
C |
T |
1: 79,414,069 (GRCm39) |
R218H |
probably damaging |
Het |
Shank2 |
A |
G |
7: 143,622,535 (GRCm39) |
H223R |
possibly damaging |
Het |
Slc23a2 |
A |
T |
2: 131,913,842 (GRCm39) |
F312I |
probably damaging |
Het |
Slc24a1 |
T |
A |
9: 64,835,394 (GRCm39) |
E911V |
probably damaging |
Het |
St8sia4 |
CCTCT |
CCT |
1: 95,555,232 (GRCm39) |
|
probably null |
Het |
Stat1 |
C |
A |
1: 52,174,831 (GRCm39) |
Q178K |
probably benign |
Het |
Stat6 |
A |
C |
10: 127,483,661 (GRCm39) |
N75T |
probably benign |
Het |
Stk10 |
G |
T |
11: 32,538,915 (GRCm39) |
K251N |
|
Het |
Sult1e1 |
G |
T |
5: 87,737,973 (GRCm39) |
A36E |
probably damaging |
Het |
Tbc1d12 |
A |
G |
19: 38,899,477 (GRCm39) |
S466G |
probably benign |
Het |
Thsd4 |
C |
A |
9: 59,964,230 (GRCm39) |
A421S |
probably benign |
Het |
Tsga10 |
T |
A |
1: 37,873,364 (GRCm39) |
I172L |
probably benign |
Het |
Ttn |
A |
T |
2: 76,600,856 (GRCm39) |
M18842K |
probably benign |
Het |
Ttpal |
T |
G |
2: 163,449,105 (GRCm39) |
|
probably benign |
Het |
Twf2 |
A |
G |
9: 106,088,999 (GRCm39) |
D62G |
probably benign |
Het |
Ube3d |
C |
A |
9: 86,254,501 (GRCm39) |
V327F |
probably damaging |
Het |
Ugt1a8 |
T |
C |
1: 88,015,706 (GRCm39) |
S40P |
probably benign |
Het |
Unc13c |
A |
T |
9: 73,424,553 (GRCm39) |
I2021N |
possibly damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,167,849 (GRCm39) |
Y701F |
probably benign |
Het |
|
Other mutations in Myh8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01020:Myh8
|
APN |
11 |
67,174,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01348:Myh8
|
APN |
11 |
67,188,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01382:Myh8
|
APN |
11 |
67,192,799 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01454:Myh8
|
APN |
11 |
67,174,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Myh8
|
APN |
11 |
67,183,505 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01472:Myh8
|
APN |
11 |
67,179,205 (GRCm39) |
splice site |
probably benign |
|
IGL01473:Myh8
|
APN |
11 |
67,192,651 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01613:Myh8
|
APN |
11 |
67,192,536 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01763:Myh8
|
APN |
11 |
67,177,245 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01828:Myh8
|
APN |
11 |
67,194,652 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01862:Myh8
|
APN |
11 |
67,180,520 (GRCm39) |
nonsense |
probably null |
|
IGL01905:Myh8
|
APN |
11 |
67,175,477 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02280:Myh8
|
APN |
11 |
67,174,198 (GRCm39) |
unclassified |
probably benign |
|
IGL02386:Myh8
|
APN |
11 |
67,185,266 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02449:Myh8
|
APN |
11 |
67,185,440 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02500:Myh8
|
APN |
11 |
67,196,536 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02745:Myh8
|
APN |
11 |
67,188,327 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02799:Myh8
|
APN |
11 |
67,192,418 (GRCm39) |
splice site |
probably benign |
|
IGL03063:Myh8
|
APN |
11 |
67,179,031 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03223:Myh8
|
APN |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03336:Myh8
|
APN |
11 |
67,175,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03338:Myh8
|
APN |
11 |
67,189,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03351:Myh8
|
APN |
11 |
67,194,739 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03392:Myh8
|
APN |
11 |
67,185,244 (GRCm39) |
missense |
probably damaging |
1.00 |
BB003:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB009:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
BB013:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
BB019:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Myh8
|
UTSW |
11 |
67,180,456 (GRCm39) |
missense |
probably benign |
0.01 |
R0012:Myh8
|
UTSW |
11 |
67,190,847 (GRCm39) |
missense |
probably benign |
0.02 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Myh8
|
UTSW |
11 |
67,189,351 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Myh8
|
UTSW |
11 |
67,197,090 (GRCm39) |
splice site |
probably benign |
|
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0131:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0132:Myh8
|
UTSW |
11 |
67,183,014 (GRCm39) |
missense |
probably damaging |
0.96 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0238:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0239:Myh8
|
UTSW |
11 |
67,192,518 (GRCm39) |
missense |
probably benign |
0.00 |
R0393:Myh8
|
UTSW |
11 |
67,196,843 (GRCm39) |
splice site |
probably benign |
|
R0453:Myh8
|
UTSW |
11 |
67,183,731 (GRCm39) |
missense |
probably benign |
0.03 |
R0454:Myh8
|
UTSW |
11 |
67,194,591 (GRCm39) |
nonsense |
probably null |
|
R0466:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R0487:Myh8
|
UTSW |
11 |
67,192,837 (GRCm39) |
missense |
probably benign |
|
R0511:Myh8
|
UTSW |
11 |
67,175,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0557:Myh8
|
UTSW |
11 |
67,192,624 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0589:Myh8
|
UTSW |
11 |
67,189,453 (GRCm39) |
missense |
probably benign |
0.00 |
R0658:Myh8
|
UTSW |
11 |
67,175,358 (GRCm39) |
critical splice donor site |
probably null |
|
R0782:Myh8
|
UTSW |
11 |
67,180,580 (GRCm39) |
missense |
probably benign |
0.16 |
R0829:Myh8
|
UTSW |
11 |
67,174,326 (GRCm39) |
unclassified |
probably benign |
|
R0845:Myh8
|
UTSW |
11 |
67,177,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0930:Myh8
|
UTSW |
11 |
67,196,824 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0972:Myh8
|
UTSW |
11 |
67,188,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R1132:Myh8
|
UTSW |
11 |
67,187,957 (GRCm39) |
nonsense |
probably null |
|
R1417:Myh8
|
UTSW |
11 |
67,197,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R1478:Myh8
|
UTSW |
11 |
67,183,551 (GRCm39) |
missense |
probably benign |
0.23 |
R1497:Myh8
|
UTSW |
11 |
67,180,638 (GRCm39) |
missense |
probably benign |
0.00 |
R1605:Myh8
|
UTSW |
11 |
67,192,497 (GRCm39) |
missense |
probably damaging |
0.99 |
R1701:Myh8
|
UTSW |
11 |
67,170,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R1950:Myh8
|
UTSW |
11 |
67,169,830 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1989:Myh8
|
UTSW |
11 |
67,183,550 (GRCm39) |
missense |
probably benign |
0.00 |
R2010:Myh8
|
UTSW |
11 |
67,187,990 (GRCm39) |
nonsense |
probably null |
|
R2095:Myh8
|
UTSW |
11 |
67,177,050 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Myh8
|
UTSW |
11 |
67,183,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R2152:Myh8
|
UTSW |
11 |
67,185,295 (GRCm39) |
missense |
probably damaging |
0.97 |
R2229:Myh8
|
UTSW |
11 |
67,199,174 (GRCm39) |
missense |
probably damaging |
0.98 |
R2302:Myh8
|
UTSW |
11 |
67,177,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Myh8
|
UTSW |
11 |
67,185,344 (GRCm39) |
missense |
probably benign |
0.03 |
R2429:Myh8
|
UTSW |
11 |
67,194,723 (GRCm39) |
missense |
probably benign |
0.21 |
R2880:Myh8
|
UTSW |
11 |
67,188,090 (GRCm39) |
missense |
probably damaging |
0.97 |
R3692:Myh8
|
UTSW |
11 |
67,192,744 (GRCm39) |
missense |
probably damaging |
0.98 |
R3756:Myh8
|
UTSW |
11 |
67,175,443 (GRCm39) |
unclassified |
probably benign |
|
R3924:Myh8
|
UTSW |
11 |
67,187,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R4172:Myh8
|
UTSW |
11 |
67,183,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R4255:Myh8
|
UTSW |
11 |
67,190,560 (GRCm39) |
missense |
probably benign |
|
R4621:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Myh8
|
UTSW |
11 |
67,177,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Myh8
|
UTSW |
11 |
67,170,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R4914:Myh8
|
UTSW |
11 |
67,183,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Myh8
|
UTSW |
11 |
67,196,742 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5119:Myh8
|
UTSW |
11 |
67,189,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R5159:Myh8
|
UTSW |
11 |
67,179,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R5229:Myh8
|
UTSW |
11 |
67,175,310 (GRCm39) |
missense |
probably damaging |
0.96 |
R5320:Myh8
|
UTSW |
11 |
67,177,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Myh8
|
UTSW |
11 |
67,192,244 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5523:Myh8
|
UTSW |
11 |
67,196,788 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5540:Myh8
|
UTSW |
11 |
67,177,266 (GRCm39) |
missense |
probably benign |
0.00 |
R5726:Myh8
|
UTSW |
11 |
67,185,392 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5770:Myh8
|
UTSW |
11 |
67,188,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R6135:Myh8
|
UTSW |
11 |
67,188,326 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6253:Myh8
|
UTSW |
11 |
67,192,793 (GRCm39) |
missense |
probably benign |
0.06 |
R6318:Myh8
|
UTSW |
11 |
67,190,167 (GRCm39) |
missense |
probably benign |
0.00 |
R6432:Myh8
|
UTSW |
11 |
67,189,405 (GRCm39) |
missense |
probably benign |
0.01 |
R6452:Myh8
|
UTSW |
11 |
67,196,565 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6452:Myh8
|
UTSW |
11 |
67,183,275 (GRCm39) |
missense |
probably benign |
0.27 |
R6512:Myh8
|
UTSW |
11 |
67,180,488 (GRCm39) |
nonsense |
probably null |
|
R6714:Myh8
|
UTSW |
11 |
67,197,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Myh8
|
UTSW |
11 |
67,175,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:Myh8
|
UTSW |
11 |
67,179,142 (GRCm39) |
missense |
probably benign |
0.03 |
R7025:Myh8
|
UTSW |
11 |
67,188,365 (GRCm39) |
missense |
probably benign |
0.02 |
R7086:Myh8
|
UTSW |
11 |
67,183,453 (GRCm39) |
splice site |
probably null |
|
R7098:Myh8
|
UTSW |
11 |
67,169,879 (GRCm39) |
missense |
probably benign |
0.03 |
R7498:Myh8
|
UTSW |
11 |
67,174,263 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7716:Myh8
|
UTSW |
11 |
67,189,478 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7765:Myh8
|
UTSW |
11 |
67,194,481 (GRCm39) |
missense |
probably benign |
0.44 |
R7825:Myh8
|
UTSW |
11 |
67,194,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7921:Myh8
|
UTSW |
11 |
67,174,644 (GRCm39) |
missense |
probably damaging |
0.97 |
R7926:Myh8
|
UTSW |
11 |
67,169,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7932:Myh8
|
UTSW |
11 |
67,185,430 (GRCm39) |
missense |
probably benign |
0.00 |
R8003:Myh8
|
UTSW |
11 |
67,190,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R8028:Myh8
|
UTSW |
11 |
67,194,502 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8121:Myh8
|
UTSW |
11 |
67,180,647 (GRCm39) |
missense |
probably benign |
0.00 |
R8125:Myh8
|
UTSW |
11 |
67,190,598 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8170:Myh8
|
UTSW |
11 |
67,179,092 (GRCm39) |
missense |
probably benign |
0.30 |
R8277:Myh8
|
UTSW |
11 |
67,183,735 (GRCm39) |
missense |
probably benign |
0.10 |
R8304:Myh8
|
UTSW |
11 |
67,195,162 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8431:Myh8
|
UTSW |
11 |
67,174,440 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8535:Myh8
|
UTSW |
11 |
67,169,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Myh8
|
UTSW |
11 |
67,174,203 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8858:Myh8
|
UTSW |
11 |
67,192,820 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8927:Myh8
|
UTSW |
11 |
67,174,081 (GRCm39) |
missense |
probably benign |
0.10 |
R8928:Myh8
|
UTSW |
11 |
67,174,081 (GRCm39) |
missense |
probably benign |
0.10 |
R9031:Myh8
|
UTSW |
11 |
67,190,141 (GRCm39) |
missense |
possibly damaging |
0.49 |
R9172:Myh8
|
UTSW |
11 |
67,183,260 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9365:Myh8
|
UTSW |
11 |
67,174,632 (GRCm39) |
missense |
probably benign |
0.42 |
R9468:Myh8
|
UTSW |
11 |
67,197,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R9564:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
R9565:Myh8
|
UTSW |
11 |
67,177,215 (GRCm39) |
missense |
probably benign |
0.40 |
T0722:Myh8
|
UTSW |
11 |
67,195,262 (GRCm39) |
missense |
probably benign |
0.41 |
Z1088:Myh8
|
UTSW |
11 |
67,189,418 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myh8
|
UTSW |
11 |
67,194,500 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myh8
|
UTSW |
11 |
67,199,181 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1177:Myh8
|
UTSW |
11 |
67,192,250 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1187:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1188:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1190:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
Z1191:Myh8
|
UTSW |
11 |
67,188,312 (GRCm39) |
missense |
probably benign |
|
|