Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Armc8 |
A |
G |
9: 99,378,202 (GRCm39) |
|
probably null |
Het |
Asxl1 |
A |
G |
2: 153,241,409 (GRCm39) |
E653G |
probably damaging |
Het |
AW551984 |
G |
A |
9: 39,504,118 (GRCm39) |
A616V |
probably benign |
Het |
Birc6 |
T |
C |
17: 75,004,420 (GRCm39) |
M4763T |
possibly damaging |
Het |
Bltp1 |
T |
A |
3: 36,975,509 (GRCm39) |
M727K |
probably benign |
Het |
Cand2 |
T |
G |
6: 115,774,893 (GRCm39) |
F1034V |
probably damaging |
Het |
Ccdc80 |
T |
C |
16: 44,936,741 (GRCm39) |
V722A |
possibly damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Chrnd |
G |
A |
1: 87,125,380 (GRCm39) |
V340I |
possibly damaging |
Het |
Clip1 |
T |
C |
5: 123,751,366 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 47,513,617 (GRCm39) |
E1920G |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 48,403,729 (GRCm39) |
F194I |
probably damaging |
Het |
D930048N14Rik |
T |
A |
11: 51,544,556 (GRCm39) |
|
probably null |
Het |
Defa28 |
T |
C |
8: 22,073,863 (GRCm39) |
Y89H |
probably benign |
Het |
Dnah1 |
C |
T |
14: 30,996,001 (GRCm39) |
G2705E |
probably damaging |
Het |
Eci2 |
A |
T |
13: 35,174,250 (GRCm39) |
S104T |
possibly damaging |
Het |
Ep300 |
T |
C |
15: 81,485,696 (GRCm39) |
S228P |
unknown |
Het |
Gabrb2 |
T |
A |
11: 42,378,201 (GRCm39) |
M139K |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,266,265 (GRCm39) |
N592I |
possibly damaging |
Het |
Gpr158 |
C |
T |
2: 21,751,520 (GRCm39) |
R480C |
probably damaging |
Het |
Gps1 |
A |
G |
11: 120,676,008 (GRCm39) |
D71G |
probably benign |
Het |
Hoxc9 |
T |
C |
15: 102,890,313 (GRCm39) |
Y77H |
possibly damaging |
Het |
Il9r |
T |
A |
11: 32,143,263 (GRCm39) |
Y231F |
probably benign |
Het |
Klhl1 |
A |
G |
14: 96,438,816 (GRCm39) |
M494T |
probably benign |
Het |
Kmt2c |
A |
G |
5: 25,519,015 (GRCm39) |
V2365A |
probably benign |
Het |
Kri1 |
T |
A |
9: 21,192,425 (GRCm39) |
K241M |
possibly damaging |
Het |
Macf1 |
A |
T |
4: 123,397,018 (GRCm39) |
C928S |
probably damaging |
Het |
Mcm2 |
T |
C |
6: 88,870,073 (GRCm39) |
D32G |
probably damaging |
Het |
Mex3d |
T |
C |
10: 80,217,379 (GRCm39) |
T613A |
probably benign |
Het |
Mptx2 |
G |
A |
1: 173,102,414 (GRCm39) |
L92F |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,675,964 (GRCm39) |
I241V |
probably benign |
Het |
Nckap1l |
G |
A |
15: 103,381,195 (GRCm39) |
A366T |
probably benign |
Het |
Or5m11 |
A |
G |
2: 85,782,168 (GRCm39) |
T254A |
possibly damaging |
Het |
Plscr5 |
A |
T |
9: 92,087,564 (GRCm39) |
K178* |
probably null |
Het |
Rapgef6 |
T |
C |
11: 54,567,220 (GRCm39) |
W857R |
possibly damaging |
Het |
Raxos1 |
G |
A |
18: 66,071,059 (GRCm39) |
|
probably benign |
Het |
Rnf145 |
G |
A |
11: 44,422,120 (GRCm39) |
V68M |
possibly damaging |
Het |
Slc66a2 |
T |
A |
18: 80,315,693 (GRCm39) |
D118E |
possibly damaging |
Het |
Synpo2 |
C |
G |
3: 122,873,879 (GRCm39) |
G1029A |
probably damaging |
Het |
Tbc1d5 |
TTGCTGCTGCTGCTGCTGCTGGTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGGTGCTGCTGCTGCTG |
17: 51,106,983 (GRCm39) |
|
probably benign |
Het |
Vmn2r14 |
T |
C |
5: 109,367,816 (GRCm39) |
Y392C |
probably damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,404,492 (GRCm39) |
F304L |
probably benign |
Het |
Zfp316 |
C |
T |
5: 143,240,132 (GRCm39) |
G629D |
probably benign |
Het |
|
Other mutations in Myo6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Myo6
|
APN |
9 |
80,199,754 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00584:Myo6
|
APN |
9 |
80,149,555 (GRCm39) |
splice site |
probably benign |
|
IGL00596:Myo6
|
APN |
9 |
80,189,025 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00778:Myo6
|
APN |
9 |
80,190,868 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01667:Myo6
|
APN |
9 |
80,197,175 (GRCm39) |
missense |
unknown |
|
IGL01939:Myo6
|
APN |
9 |
80,168,100 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02123:Myo6
|
APN |
9 |
80,171,554 (GRCm39) |
splice site |
probably benign |
|
IGL02271:Myo6
|
APN |
9 |
80,168,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02512:Myo6
|
APN |
9 |
80,199,801 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02716:Myo6
|
APN |
9 |
80,176,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02888:Myo6
|
APN |
9 |
80,177,013 (GRCm39) |
splice site |
probably benign |
|
IGL02890:Myo6
|
APN |
9 |
80,173,456 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Myo6
|
APN |
9 |
80,171,516 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02990:Myo6
|
APN |
9 |
80,183,685 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03060:Myo6
|
APN |
9 |
80,168,159 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03145:Myo6
|
APN |
9 |
80,207,947 (GRCm39) |
nonsense |
probably null |
|
IGL03306:Myo6
|
APN |
9 |
80,153,837 (GRCm39) |
missense |
probably damaging |
1.00 |
agnostic
|
UTSW |
9 |
80,190,816 (GRCm39) |
missense |
possibly damaging |
0.62 |
knownothing
|
UTSW |
9 |
80,210,583 (GRCm39) |
critical splice donor site |
probably null |
|
mayday_circler
|
UTSW |
9 |
80,153,733 (GRCm39) |
nonsense |
probably null |
|
torticollis
|
UTSW |
9 |
80,195,499 (GRCm39) |
critical splice donor site |
probably null |
|
toss
|
UTSW |
9 |
80,207,949 (GRCm39) |
critical splice donor site |
probably null |
|
truths
|
UTSW |
9 |
80,177,321 (GRCm39) |
nonsense |
probably null |
|
unbiased
|
UTSW |
9 |
80,181,257 (GRCm39) |
splice site |
probably benign |
|
IGL03134:Myo6
|
UTSW |
9 |
80,199,749 (GRCm39) |
missense |
probably damaging |
0.96 |
R0023:Myo6
|
UTSW |
9 |
80,190,816 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0023:Myo6
|
UTSW |
9 |
80,190,816 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0124:Myo6
|
UTSW |
9 |
80,215,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0133:Myo6
|
UTSW |
9 |
80,181,257 (GRCm39) |
splice site |
probably benign |
|
R0207:Myo6
|
UTSW |
9 |
80,195,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Myo6
|
UTSW |
9 |
80,190,861 (GRCm39) |
missense |
probably damaging |
0.98 |
R0389:Myo6
|
UTSW |
9 |
80,199,748 (GRCm39) |
missense |
probably damaging |
0.98 |
R0432:Myo6
|
UTSW |
9 |
80,181,256 (GRCm39) |
splice site |
probably benign |
|
R0526:Myo6
|
UTSW |
9 |
80,190,823 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0791:Myo6
|
UTSW |
9 |
80,169,656 (GRCm39) |
splice site |
probably benign |
|
R0885:Myo6
|
UTSW |
9 |
80,149,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Myo6
|
UTSW |
9 |
80,195,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R1113:Myo6
|
UTSW |
9 |
80,152,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Myo6
|
UTSW |
9 |
80,193,664 (GRCm39) |
nonsense |
probably null |
|
R1308:Myo6
|
UTSW |
9 |
80,152,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1498:Myo6
|
UTSW |
9 |
80,214,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Myo6
|
UTSW |
9 |
80,195,499 (GRCm39) |
critical splice donor site |
probably null |
|
R1615:Myo6
|
UTSW |
9 |
80,215,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Myo6
|
UTSW |
9 |
80,193,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Myo6
|
UTSW |
9 |
80,177,331 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1789:Myo6
|
UTSW |
9 |
80,207,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Myo6
|
UTSW |
9 |
80,168,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R1978:Myo6
|
UTSW |
9 |
80,136,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R2011:Myo6
|
UTSW |
9 |
80,215,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R2092:Myo6
|
UTSW |
9 |
80,152,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R2098:Myo6
|
UTSW |
9 |
80,188,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R2206:Myo6
|
UTSW |
9 |
80,165,737 (GRCm39) |
missense |
probably benign |
0.01 |
R2286:Myo6
|
UTSW |
9 |
80,173,494 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2429:Myo6
|
UTSW |
9 |
80,210,583 (GRCm39) |
critical splice donor site |
probably null |
|
R2696:Myo6
|
UTSW |
9 |
80,168,176 (GRCm39) |
missense |
probably benign |
0.00 |
R2897:Myo6
|
UTSW |
9 |
80,176,893 (GRCm39) |
splice site |
probably null |
|
R2898:Myo6
|
UTSW |
9 |
80,176,893 (GRCm39) |
splice site |
probably null |
|
R3881:Myo6
|
UTSW |
9 |
80,171,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Myo6
|
UTSW |
9 |
80,195,320 (GRCm39) |
missense |
probably benign |
0.26 |
R4718:Myo6
|
UTSW |
9 |
80,153,799 (GRCm39) |
missense |
probably benign |
0.01 |
R4893:Myo6
|
UTSW |
9 |
80,136,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R4936:Myo6
|
UTSW |
9 |
80,214,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Myo6
|
UTSW |
9 |
80,190,792 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5073:Myo6
|
UTSW |
9 |
80,195,290 (GRCm39) |
missense |
probably benign |
0.00 |
R5101:Myo6
|
UTSW |
9 |
80,177,321 (GRCm39) |
nonsense |
probably null |
|
R5137:Myo6
|
UTSW |
9 |
80,149,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Myo6
|
UTSW |
9 |
80,183,656 (GRCm39) |
nonsense |
probably null |
|
R5510:Myo6
|
UTSW |
9 |
80,152,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Myo6
|
UTSW |
9 |
80,125,002 (GRCm39) |
missense |
probably damaging |
0.99 |
R5693:Myo6
|
UTSW |
9 |
80,173,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R6693:Myo6
|
UTSW |
9 |
80,153,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Myo6
|
UTSW |
9 |
80,152,418 (GRCm39) |
missense |
unknown |
|
R7399:Myo6
|
UTSW |
9 |
80,169,573 (GRCm39) |
missense |
unknown |
|
R7492:Myo6
|
UTSW |
9 |
80,195,328 (GRCm39) |
nonsense |
probably null |
|
R7651:Myo6
|
UTSW |
9 |
80,171,548 (GRCm39) |
critical splice donor site |
probably null |
|
R7698:Myo6
|
UTSW |
9 |
80,124,938 (GRCm39) |
missense |
unknown |
|
R7743:Myo6
|
UTSW |
9 |
80,183,611 (GRCm39) |
missense |
unknown |
|
R7888:Myo6
|
UTSW |
9 |
80,203,947 (GRCm39) |
missense |
probably damaging |
0.99 |
R8161:Myo6
|
UTSW |
9 |
80,124,991 (GRCm39) |
missense |
unknown |
|
R8245:Myo6
|
UTSW |
9 |
80,162,229 (GRCm39) |
missense |
unknown |
|
R8375:Myo6
|
UTSW |
9 |
80,162,206 (GRCm39) |
missense |
unknown |
|
R8387:Myo6
|
UTSW |
9 |
80,183,632 (GRCm39) |
missense |
unknown |
|
R8467:Myo6
|
UTSW |
9 |
80,136,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R8669:Myo6
|
UTSW |
9 |
80,173,531 (GRCm39) |
missense |
unknown |
|
R8770:Myo6
|
UTSW |
9 |
80,171,481 (GRCm39) |
missense |
unknown |
|
R8807:Myo6
|
UTSW |
9 |
80,207,949 (GRCm39) |
critical splice donor site |
probably null |
|
R9006:Myo6
|
UTSW |
9 |
80,136,140 (GRCm39) |
missense |
unknown |
|
R9018:Myo6
|
UTSW |
9 |
80,159,086 (GRCm39) |
missense |
unknown |
|
R9038:Myo6
|
UTSW |
9 |
80,162,285 (GRCm39) |
missense |
unknown |
|
R9124:Myo6
|
UTSW |
9 |
80,195,353 (GRCm39) |
missense |
unknown |
|
R9190:Myo6
|
UTSW |
9 |
80,195,384 (GRCm39) |
missense |
unknown |
|
R9194:Myo6
|
UTSW |
9 |
80,153,836 (GRCm39) |
missense |
unknown |
|
R9281:Myo6
|
UTSW |
9 |
80,162,164 (GRCm39) |
nonsense |
probably null |
|
Z1191:Myo6
|
UTSW |
9 |
80,149,509 (GRCm39) |
nonsense |
probably null |
|
|