Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acta2 |
A |
G |
19: 34,229,191 (GRCm39) |
I66T |
probably damaging |
Het |
Actl11 |
T |
C |
9: 107,806,247 (GRCm39) |
V190A |
probably benign |
Het |
Ankub1 |
T |
A |
3: 57,597,817 (GRCm39) |
Y51F |
possibly damaging |
Het |
Armh3 |
A |
T |
19: 45,928,915 (GRCm39) |
L393H |
probably damaging |
Het |
Ccdc63 |
G |
A |
5: 122,249,027 (GRCm39) |
S434L |
possibly damaging |
Het |
Cdan1 |
T |
A |
2: 120,556,134 (GRCm39) |
I711F |
possibly damaging |
Het |
Cep170b |
C |
A |
12: 112,710,594 (GRCm39) |
N1474K |
probably damaging |
Het |
Cyp2c40 |
A |
G |
19: 39,775,254 (GRCm39) |
S333P |
probably damaging |
Het |
Dars1 |
A |
G |
1: 128,343,081 (GRCm39) |
|
probably benign |
Het |
Dock3 |
T |
A |
9: 106,909,563 (GRCm39) |
|
probably benign |
Het |
Dsp |
A |
G |
13: 38,360,471 (GRCm39) |
I359V |
possibly damaging |
Het |
Fut8 |
T |
G |
12: 77,497,032 (GRCm39) |
L414* |
probably null |
Het |
Gja1 |
A |
G |
10: 56,264,544 (GRCm39) |
Y301C |
probably damaging |
Het |
Glipr1l1 |
T |
C |
10: 111,908,184 (GRCm39) |
S161P |
probably damaging |
Het |
Gpat4 |
A |
T |
8: 23,665,354 (GRCm39) |
|
probably null |
Het |
Grhl1 |
T |
A |
12: 24,658,577 (GRCm39) |
|
probably null |
Het |
Hectd3 |
T |
C |
4: 116,853,569 (GRCm39) |
V181A |
possibly damaging |
Het |
Htr2a |
T |
A |
14: 74,943,194 (GRCm39) |
I258N |
probably damaging |
Het |
Hyou1 |
T |
A |
9: 44,292,414 (GRCm39) |
D83E |
possibly damaging |
Het |
Nkx2-2 |
T |
C |
2: 147,027,833 (GRCm39) |
S36G |
probably benign |
Het |
Nsun2 |
T |
A |
13: 69,771,368 (GRCm39) |
V326E |
probably benign |
Het |
Nuak2 |
T |
C |
1: 132,259,308 (GRCm39) |
V362A |
probably benign |
Het |
Nyap2 |
G |
A |
1: 81,169,642 (GRCm39) |
C133Y |
probably damaging |
Het |
Oas2 |
T |
C |
5: 120,879,288 (GRCm39) |
T351A |
probably benign |
Het |
Or11m3 |
C |
T |
15: 98,396,076 (GRCm39) |
T241I |
probably damaging |
Het |
Or5m13 |
T |
C |
2: 85,748,908 (GRCm39) |
I213T |
probably benign |
Het |
Pde4d |
A |
T |
13: 110,074,606 (GRCm39) |
I404F |
probably damaging |
Het |
Pga5 |
A |
G |
19: 10,652,456 (GRCm39) |
S95P |
probably damaging |
Het |
Pitpnm2 |
A |
T |
5: 124,261,257 (GRCm39) |
D947E |
probably damaging |
Het |
Pla2g10 |
C |
T |
16: 13,545,950 (GRCm39) |
R28H |
probably damaging |
Het |
Prlr |
A |
G |
15: 10,317,676 (GRCm39) |
D84G |
probably damaging |
Het |
Rbm15b |
C |
T |
9: 106,762,908 (GRCm39) |
G420D |
probably damaging |
Het |
Tbcd |
A |
G |
11: 121,496,153 (GRCm39) |
T1063A |
probably benign |
Het |
Tmc2 |
C |
T |
2: 130,102,144 (GRCm39) |
Q770* |
probably null |
Het |
Tpo |
T |
C |
12: 30,169,399 (GRCm39) |
|
probably benign |
Het |
Vim |
A |
G |
2: 13,579,624 (GRCm39) |
N128D |
probably damaging |
Het |
Vmn1r21 |
A |
T |
6: 57,821,222 (GRCm39) |
I74N |
probably damaging |
Het |
Vmn2r52 |
A |
C |
7: 9,893,107 (GRCm39) |
I677M |
probably damaging |
Het |
|
Other mutations in Myh10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00540:Myh10
|
APN |
11 |
68,681,534 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01132:Myh10
|
APN |
11 |
68,659,094 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01348:Myh10
|
APN |
11 |
68,702,629 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01404:Myh10
|
APN |
11 |
68,642,866 (GRCm39) |
splice site |
probably null |
|
IGL01409:Myh10
|
APN |
11 |
68,698,045 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02111:Myh10
|
APN |
11 |
68,680,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02481:Myh10
|
APN |
11 |
68,692,994 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02483:Myh10
|
APN |
11 |
68,692,994 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02502:Myh10
|
APN |
11 |
68,705,198 (GRCm39) |
splice site |
probably null |
|
IGL03178:Myh10
|
APN |
11 |
68,590,239 (GRCm39) |
missense |
probably benign |
0.19 |
algia
|
UTSW |
11 |
68,693,757 (GRCm39) |
missense |
probably damaging |
1.00 |
itis
|
UTSW |
11 |
68,655,071 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4802001:Myh10
|
UTSW |
11 |
68,655,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Myh10
|
UTSW |
11 |
68,590,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Myh10
|
UTSW |
11 |
68,590,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Myh10
|
UTSW |
11 |
68,702,425 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0855:Myh10
|
UTSW |
11 |
68,702,627 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1110:Myh10
|
UTSW |
11 |
68,682,676 (GRCm39) |
splice site |
probably benign |
|
R1135:Myh10
|
UTSW |
11 |
68,698,023 (GRCm39) |
missense |
probably benign |
|
R1169:Myh10
|
UTSW |
11 |
68,653,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R1643:Myh10
|
UTSW |
11 |
68,682,836 (GRCm39) |
missense |
probably damaging |
0.96 |
R1733:Myh10
|
UTSW |
11 |
68,693,122 (GRCm39) |
missense |
probably benign |
0.06 |
R1754:Myh10
|
UTSW |
11 |
68,703,884 (GRCm39) |
missense |
probably damaging |
0.98 |
R1859:Myh10
|
UTSW |
11 |
68,636,239 (GRCm39) |
missense |
probably benign |
0.03 |
R1898:Myh10
|
UTSW |
11 |
68,662,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Myh10
|
UTSW |
11 |
68,662,694 (GRCm39) |
splice site |
probably benign |
|
R1914:Myh10
|
UTSW |
11 |
68,681,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R1915:Myh10
|
UTSW |
11 |
68,681,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R1987:Myh10
|
UTSW |
11 |
68,705,322 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2130:Myh10
|
UTSW |
11 |
68,698,115 (GRCm39) |
splice site |
probably benign |
|
R2132:Myh10
|
UTSW |
11 |
68,698,115 (GRCm39) |
splice site |
probably benign |
|
R2136:Myh10
|
UTSW |
11 |
68,695,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Myh10
|
UTSW |
11 |
68,673,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R2351:Myh10
|
UTSW |
11 |
68,683,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R3407:Myh10
|
UTSW |
11 |
68,681,037 (GRCm39) |
missense |
possibly damaging |
0.68 |
R3721:Myh10
|
UTSW |
11 |
68,703,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R3908:Myh10
|
UTSW |
11 |
68,661,885 (GRCm39) |
critical splice donor site |
probably null |
|
R4275:Myh10
|
UTSW |
11 |
68,642,766 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4526:Myh10
|
UTSW |
11 |
68,705,875 (GRCm39) |
missense |
probably benign |
0.04 |
R4666:Myh10
|
UTSW |
11 |
68,692,556 (GRCm39) |
critical splice donor site |
probably null |
|
R4668:Myh10
|
UTSW |
11 |
68,695,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Myh10
|
UTSW |
11 |
68,676,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4968:Myh10
|
UTSW |
11 |
68,684,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Myh10
|
UTSW |
11 |
68,689,197 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5201:Myh10
|
UTSW |
11 |
68,674,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R5288:Myh10
|
UTSW |
11 |
68,692,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Myh10
|
UTSW |
11 |
68,655,071 (GRCm39) |
missense |
probably damaging |
0.96 |
R5366:Myh10
|
UTSW |
11 |
68,651,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R5384:Myh10
|
UTSW |
11 |
68,692,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R5427:Myh10
|
UTSW |
11 |
68,693,757 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Myh10
|
UTSW |
11 |
68,689,206 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5551:Myh10
|
UTSW |
11 |
68,659,113 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5777:Myh10
|
UTSW |
11 |
68,676,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R5995:Myh10
|
UTSW |
11 |
68,705,809 (GRCm39) |
missense |
probably benign |
0.01 |
R6021:Myh10
|
UTSW |
11 |
68,699,688 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6171:Myh10
|
UTSW |
11 |
68,682,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R6179:Myh10
|
UTSW |
11 |
68,692,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R6263:Myh10
|
UTSW |
11 |
68,701,058 (GRCm39) |
missense |
probably damaging |
0.98 |
R6264:Myh10
|
UTSW |
11 |
68,636,241 (GRCm39) |
missense |
probably benign |
0.01 |
R6484:Myh10
|
UTSW |
11 |
68,590,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6575:Myh10
|
UTSW |
11 |
68,699,676 (GRCm39) |
missense |
probably benign |
0.00 |
R6736:Myh10
|
UTSW |
11 |
68,636,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Myh10
|
UTSW |
11 |
68,692,965 (GRCm39) |
missense |
probably benign |
|
R7256:Myh10
|
UTSW |
11 |
68,681,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R7329:Myh10
|
UTSW |
11 |
68,701,017 (GRCm39) |
missense |
probably benign |
0.44 |
R7363:Myh10
|
UTSW |
11 |
68,705,874 (GRCm39) |
missense |
probably benign |
|
R7576:Myh10
|
UTSW |
11 |
68,692,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Myh10
|
UTSW |
11 |
68,636,806 (GRCm39) |
missense |
unknown |
|
R7681:Myh10
|
UTSW |
11 |
68,662,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R7813:Myh10
|
UTSW |
11 |
68,676,735 (GRCm39) |
missense |
probably benign |
0.00 |
R7834:Myh10
|
UTSW |
11 |
68,676,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Myh10
|
UTSW |
11 |
68,699,719 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7938:Myh10
|
UTSW |
11 |
68,583,327 (GRCm39) |
missense |
unknown |
|
R7958:Myh10
|
UTSW |
11 |
68,612,173 (GRCm39) |
missense |
probably benign |
0.00 |
R7994:Myh10
|
UTSW |
11 |
68,681,070 (GRCm39) |
critical splice donor site |
probably null |
|
R8395:Myh10
|
UTSW |
11 |
68,682,842 (GRCm39) |
missense |
probably damaging |
0.98 |
R8523:Myh10
|
UTSW |
11 |
68,688,235 (GRCm39) |
missense |
probably benign |
0.01 |
R8674:Myh10
|
UTSW |
11 |
68,705,257 (GRCm39) |
missense |
probably damaging |
0.98 |
R8816:Myh10
|
UTSW |
11 |
68,693,778 (GRCm39) |
missense |
probably damaging |
0.97 |
R8912:Myh10
|
UTSW |
11 |
68,680,929 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9057:Myh10
|
UTSW |
11 |
68,656,011 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9333:Myh10
|
UTSW |
11 |
68,680,980 (GRCm39) |
missense |
probably benign |
0.12 |
R9586:Myh10
|
UTSW |
11 |
68,703,820 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9617:Myh10
|
UTSW |
11 |
68,682,815 (GRCm39) |
missense |
probably benign |
0.21 |
X0028:Myh10
|
UTSW |
11 |
68,683,961 (GRCm39) |
missense |
probably damaging |
1.00 |
|