Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp7 |
T |
C |
7: 28,328,914 (GRCm39) |
T31A |
probably benign |
Het |
Aldh16a1 |
G |
A |
7: 44,795,459 (GRCm39) |
P400L |
probably damaging |
Het |
Ampd3 |
T |
C |
7: 110,401,766 (GRCm39) |
V429A |
possibly damaging |
Het |
Brd8 |
C |
T |
18: 34,735,780 (GRCm39) |
S899N |
probably damaging |
Het |
Cldn11 |
C |
T |
3: 31,204,336 (GRCm39) |
T13M |
probably benign |
Het |
Cngb3 |
C |
A |
4: 19,367,801 (GRCm39) |
Q237K |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,569,740 (GRCm39) |
|
probably null |
Het |
Copa |
T |
A |
1: 171,939,695 (GRCm39) |
L621H |
probably damaging |
Het |
Dbn1 |
T |
C |
13: 55,624,553 (GRCm39) |
D332G |
possibly damaging |
Het |
Drc1 |
T |
C |
5: 30,504,448 (GRCm39) |
S197P |
probably benign |
Het |
E2f2 |
A |
G |
4: 135,900,159 (GRCm39) |
N23S |
probably benign |
Het |
Epb41l2 |
T |
A |
10: 25,336,742 (GRCm39) |
L246H |
probably damaging |
Het |
Fam13b |
G |
A |
18: 34,578,671 (GRCm39) |
|
probably benign |
Het |
Fam184b |
A |
G |
5: 45,796,493 (GRCm39) |
M30T |
possibly damaging |
Het |
Fn3krp |
G |
A |
11: 121,320,270 (GRCm39) |
R205H |
probably benign |
Het |
Fndc11 |
A |
G |
2: 180,863,443 (GRCm39) |
I83V |
probably benign |
Het |
Garin2 |
T |
C |
12: 78,780,981 (GRCm39) |
|
probably null |
Het |
Gm3629 |
C |
T |
14: 17,834,541 (GRCm39) |
R150H |
probably benign |
Het |
Hs6st1 |
T |
A |
1: 36,142,952 (GRCm39) |
F296I |
possibly damaging |
Het |
Igsf10 |
T |
A |
3: 59,226,081 (GRCm39) |
I2531F |
probably damaging |
Het |
Klhl40 |
T |
C |
9: 121,608,989 (GRCm39) |
F385L |
probably benign |
Het |
Krt87 |
A |
T |
15: 101,385,466 (GRCm39) |
M302K |
possibly damaging |
Het |
Lrrc43 |
A |
T |
5: 123,632,342 (GRCm39) |
I162F |
probably damaging |
Het |
Map3k21 |
A |
G |
8: 126,652,849 (GRCm39) |
E325G |
probably damaging |
Het |
Mpo |
A |
T |
11: 87,685,621 (GRCm39) |
N33I |
probably benign |
Het |
Mpp4 |
A |
G |
1: 59,200,625 (GRCm39) |
|
probably null |
Het |
Muc5b |
C |
T |
7: 141,417,494 (GRCm39) |
T3480I |
possibly damaging |
Het |
Nostrin |
C |
T |
2: 68,986,453 (GRCm39) |
|
probably benign |
Het |
Nphp1 |
T |
C |
2: 127,595,969 (GRCm39) |
M498V |
probably benign |
Het |
Nr4a2 |
A |
T |
2: 57,001,667 (GRCm39) |
L199Q |
possibly damaging |
Het |
Pcdhb6 |
A |
T |
18: 37,468,873 (GRCm39) |
N598I |
probably damaging |
Het |
Pex19 |
T |
A |
1: 171,961,853 (GRCm39) |
M207K |
probably damaging |
Het |
Pfkfb4 |
C |
T |
9: 108,854,178 (GRCm39) |
R351W |
probably damaging |
Het |
Plekha2 |
T |
C |
8: 25,532,745 (GRCm39) |
K409E |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,476,691 (GRCm39) |
L1169P |
probably damaging |
Het |
Pmpcb |
A |
G |
5: 21,948,373 (GRCm39) |
|
probably benign |
Het |
Ptrh1 |
T |
C |
2: 32,666,826 (GRCm39) |
|
probably benign |
Het |
Rc3h2 |
T |
C |
2: 37,288,265 (GRCm39) |
E439G |
probably damaging |
Het |
Ric1 |
C |
T |
19: 29,572,200 (GRCm39) |
A665V |
probably benign |
Het |
Stx18 |
T |
A |
5: 38,285,447 (GRCm39) |
V219D |
probably damaging |
Het |
Taf7 |
A |
T |
18: 37,775,533 (GRCm39) |
|
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,415,988 (GRCm39) |
I895T |
possibly damaging |
Het |
Tbc1d8 |
A |
G |
1: 39,419,317 (GRCm39) |
S766P |
probably damaging |
Het |
Tekt3 |
C |
A |
11: 62,974,766 (GRCm39) |
H362N |
probably benign |
Het |
Tmem214 |
G |
A |
5: 31,030,090 (GRCm39) |
A296T |
probably benign |
Het |
Tmem94 |
T |
C |
11: 115,678,364 (GRCm39) |
S196P |
possibly damaging |
Het |
Vmn2r14 |
T |
C |
5: 109,367,933 (GRCm39) |
Y353C |
probably damaging |
Het |
Vmn2r9 |
G |
A |
5: 108,991,502 (GRCm39) |
L620F |
probably damaging |
Het |
Vmn2r90 |
T |
G |
17: 17,953,744 (GRCm39) |
M636R |
probably benign |
Het |
Vmn2r98 |
T |
A |
17: 19,300,941 (GRCm39) |
C648S |
probably damaging |
Het |
Zfpm2 |
G |
A |
15: 40,965,591 (GRCm39) |
C560Y |
probably damaging |
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 |
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 |
R5701:Myo6
|
UTSW |
9 |
80,165,809 (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 |
|
|