Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adora2b |
A |
G |
11: 62,156,010 (GRCm39) |
N153S |
possibly damaging |
Het |
Afm |
C |
T |
5: 90,672,765 (GRCm39) |
T200I |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,604,165 (GRCm39) |
D397G |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,998,952 (GRCm39) |
V1032A |
probably benign |
Het |
Elovl7 |
T |
G |
13: 108,410,854 (GRCm39) |
V143G |
probably damaging |
Het |
Fhl4 |
T |
C |
10: 84,934,734 (GRCm39) |
K16E |
probably damaging |
Het |
Golga1 |
C |
T |
2: 38,924,161 (GRCm39) |
C383Y |
probably benign |
Het |
Gucy1a2 |
C |
T |
9: 3,865,409 (GRCm39) |
R628* |
probably null |
Het |
Hectd4 |
A |
G |
5: 121,466,481 (GRCm39) |
D2432G |
possibly damaging |
Het |
Iqcf5 |
T |
A |
9: 106,393,189 (GRCm39) |
*149R |
probably null |
Het |
Kcnab1 |
T |
A |
3: 65,226,875 (GRCm39) |
Y185N |
probably damaging |
Het |
Lars1 |
G |
T |
18: 42,335,615 (GRCm39) |
T1167K |
probably benign |
Het |
Mib2 |
A |
T |
4: 155,739,715 (GRCm39) |
|
probably null |
Het |
Mrps2 |
T |
C |
2: 28,358,348 (GRCm39) |
V46A |
probably benign |
Het |
Myo18b |
T |
C |
5: 113,025,916 (GRCm39) |
T45A |
unknown |
Het |
Or10ag59 |
A |
G |
2: 87,405,823 (GRCm39) |
I132V |
probably damaging |
Het |
Or4k39 |
T |
A |
2: 111,239,078 (GRCm39) |
V106E |
probably damaging |
Het |
Osbp2 |
A |
T |
11: 3,667,127 (GRCm39) |
I8N |
probably damaging |
Het |
Pcdhb22 |
A |
T |
18: 37,652,974 (GRCm39) |
N481Y |
probably damaging |
Het |
Pde3a |
T |
C |
6: 141,433,263 (GRCm39) |
W765R |
probably damaging |
Het |
Phf11c |
T |
C |
14: 59,630,586 (GRCm39) |
T40A |
probably benign |
Het |
Pih1d2 |
T |
A |
9: 50,533,177 (GRCm39) |
S268R |
probably benign |
Het |
Pkd1l2 |
T |
C |
8: 117,724,913 (GRCm39) |
N2333D |
probably damaging |
Het |
Prex1 |
A |
G |
2: 166,463,165 (GRCm39) |
I62T |
probably damaging |
Het |
Ptcd2 |
T |
C |
13: 99,463,219 (GRCm39) |
N245S |
possibly damaging |
Het |
Ripor3 |
C |
A |
2: 167,822,763 (GRCm39) |
V933F |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,534,561 (GRCm39) |
S105P |
probably benign |
Het |
Sphk2 |
A |
G |
7: 45,360,480 (GRCm39) |
|
probably null |
Het |
Tfcp2 |
T |
G |
15: 100,402,320 (GRCm39) |
E492D |
probably benign |
Het |
Ttn |
C |
T |
2: 76,629,106 (GRCm39) |
V14411I |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,628,549 (GRCm39) |
Q915R |
probably damaging |
Het |
Vmn2r45 |
C |
A |
7: 8,488,556 (GRCm39) |
S158I |
probably benign |
Het |
|
Other mutations in Myo1e |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00817:Myo1e
|
APN |
9 |
70,249,430 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00833:Myo1e
|
APN |
9 |
70,246,060 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00973:Myo1e
|
APN |
9 |
70,246,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Myo1e
|
APN |
9 |
70,223,871 (GRCm39) |
splice site |
probably benign |
|
IGL01401:Myo1e
|
APN |
9 |
70,234,448 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01402:Myo1e
|
APN |
9 |
70,245,048 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01404:Myo1e
|
APN |
9 |
70,245,048 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01613:Myo1e
|
APN |
9 |
70,248,555 (GRCm39) |
splice site |
probably benign |
|
IGL01738:Myo1e
|
APN |
9 |
70,266,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02233:Myo1e
|
APN |
9 |
70,291,081 (GRCm39) |
splice site |
probably benign |
|
IGL02244:Myo1e
|
APN |
9 |
70,274,971 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02440:Myo1e
|
APN |
9 |
70,254,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Myo1e
|
APN |
9 |
70,269,552 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02886:Myo1e
|
APN |
9 |
70,276,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03178:Myo1e
|
APN |
9 |
70,194,231 (GRCm39) |
missense |
possibly damaging |
0.47 |
I2288:Myo1e
|
UTSW |
9 |
70,249,379 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0036:Myo1e
|
UTSW |
9 |
70,248,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Myo1e
|
UTSW |
9 |
70,249,408 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0238:Myo1e
|
UTSW |
9 |
70,249,408 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0399:Myo1e
|
UTSW |
9 |
70,209,075 (GRCm39) |
splice site |
probably benign |
|
R0526:Myo1e
|
UTSW |
9 |
70,229,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R0599:Myo1e
|
UTSW |
9 |
70,283,942 (GRCm39) |
splice site |
probably benign |
|
R0656:Myo1e
|
UTSW |
9 |
70,274,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R1078:Myo1e
|
UTSW |
9 |
70,291,281 (GRCm39) |
missense |
probably benign |
|
R1278:Myo1e
|
UTSW |
9 |
70,306,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1300:Myo1e
|
UTSW |
9 |
70,209,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1329:Myo1e
|
UTSW |
9 |
70,246,020 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1349:Myo1e
|
UTSW |
9 |
70,194,351 (GRCm39) |
splice site |
probably benign |
|
R1463:Myo1e
|
UTSW |
9 |
70,246,038 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1656:Myo1e
|
UTSW |
9 |
70,303,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Myo1e
|
UTSW |
9 |
70,283,806 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1789:Myo1e
|
UTSW |
9 |
70,246,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R1970:Myo1e
|
UTSW |
9 |
70,276,055 (GRCm39) |
missense |
probably benign |
0.00 |
R2029:Myo1e
|
UTSW |
9 |
70,285,997 (GRCm39) |
splice site |
probably benign |
|
R2029:Myo1e
|
UTSW |
9 |
70,275,969 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2039:Myo1e
|
UTSW |
9 |
70,227,415 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2076:Myo1e
|
UTSW |
9 |
70,291,159 (GRCm39) |
missense |
probably benign |
|
R2256:Myo1e
|
UTSW |
9 |
70,285,655 (GRCm39) |
splice site |
probably null |
|
R2257:Myo1e
|
UTSW |
9 |
70,285,655 (GRCm39) |
splice site |
probably null |
|
R2323:Myo1e
|
UTSW |
9 |
70,286,040 (GRCm39) |
nonsense |
probably null |
|
R2443:Myo1e
|
UTSW |
9 |
70,234,454 (GRCm39) |
missense |
probably benign |
|
R4023:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4024:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4025:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4026:Myo1e
|
UTSW |
9 |
70,232,157 (GRCm39) |
missense |
probably benign |
|
R4151:Myo1e
|
UTSW |
9 |
70,204,633 (GRCm39) |
nonsense |
probably null |
|
R4764:Myo1e
|
UTSW |
9 |
70,250,417 (GRCm39) |
splice site |
probably null |
|
R4768:Myo1e
|
UTSW |
9 |
70,277,751 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4911:Myo1e
|
UTSW |
9 |
70,250,378 (GRCm39) |
missense |
probably benign |
|
R4995:Myo1e
|
UTSW |
9 |
70,260,554 (GRCm39) |
missense |
probably benign |
0.01 |
R4999:Myo1e
|
UTSW |
9 |
70,260,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R5228:Myo1e
|
UTSW |
9 |
70,229,640 (GRCm39) |
splice site |
probably null |
|
R5414:Myo1e
|
UTSW |
9 |
70,229,640 (GRCm39) |
splice site |
probably null |
|
R5577:Myo1e
|
UTSW |
9 |
70,277,753 (GRCm39) |
missense |
probably benign |
0.31 |
R5851:Myo1e
|
UTSW |
9 |
70,291,086 (GRCm39) |
missense |
probably benign |
0.17 |
R6208:Myo1e
|
UTSW |
9 |
70,283,887 (GRCm39) |
missense |
probably damaging |
0.99 |
R6907:Myo1e
|
UTSW |
9 |
70,234,437 (GRCm39) |
missense |
probably benign |
|
R7084:Myo1e
|
UTSW |
9 |
70,245,083 (GRCm39) |
missense |
probably damaging |
0.96 |
R7313:Myo1e
|
UTSW |
9 |
70,266,667 (GRCm39) |
critical splice donor site |
probably null |
|
R7383:Myo1e
|
UTSW |
9 |
70,204,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Myo1e
|
UTSW |
9 |
70,234,544 (GRCm39) |
missense |
probably damaging |
0.96 |
R7962:Myo1e
|
UTSW |
9 |
70,242,501 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8309:Myo1e
|
UTSW |
9 |
70,254,045 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8510:Myo1e
|
UTSW |
9 |
70,242,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Myo1e
|
UTSW |
9 |
70,227,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8694:Myo1e
|
UTSW |
9 |
70,291,172 (GRCm39) |
missense |
probably benign |
|
R8720:Myo1e
|
UTSW |
9 |
70,204,570 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9112:Myo1e
|
UTSW |
9 |
70,274,983 (GRCm39) |
missense |
probably benign |
0.25 |
R9148:Myo1e
|
UTSW |
9 |
70,283,830 (GRCm39) |
missense |
probably damaging |
0.98 |
R9156:Myo1e
|
UTSW |
9 |
70,266,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9251:Myo1e
|
UTSW |
9 |
70,276,076 (GRCm39) |
missense |
probably benign |
0.00 |
R9541:Myo1e
|
UTSW |
9 |
70,204,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R9624:Myo1e
|
UTSW |
9 |
70,303,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9660:Myo1e
|
UTSW |
9 |
70,223,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R9728:Myo1e
|
UTSW |
9 |
70,223,924 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Myo1e
|
UTSW |
9 |
70,285,555 (GRCm39) |
missense |
probably damaging |
0.99 |
X0065:Myo1e
|
UTSW |
9 |
70,285,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
|