Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9430038I01Rik |
A |
T |
7: 136,989,438 (GRCm39) |
|
probably benign |
Het |
Ankrd12 |
T |
A |
17: 66,294,222 (GRCm39) |
T404S |
probably benign |
Het |
Ap4m1 |
T |
C |
5: 138,174,538 (GRCm39) |
|
probably benign |
Het |
Atn1 |
A |
T |
6: 124,723,893 (GRCm39) |
|
probably benign |
Het |
Bcl9l |
A |
G |
9: 44,416,533 (GRCm39) |
Y202C |
possibly damaging |
Het |
Ceacam18 |
G |
T |
7: 43,288,815 (GRCm39) |
G189C |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,971,117 (GRCm39) |
W67* |
probably null |
Het |
Col2a1 |
C |
T |
15: 97,874,636 (GRCm39) |
E1334K |
unknown |
Het |
Crim1 |
A |
G |
17: 78,651,938 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
A |
G |
8: 16,441,836 (GRCm39) |
S343P |
probably benign |
Het |
D430041D05Rik |
G |
T |
2: 104,035,545 (GRCm39) |
D1594E |
possibly damaging |
Het |
Ess2 |
C |
T |
16: 17,720,135 (GRCm39) |
V406I |
probably damaging |
Het |
Gcm2 |
C |
T |
13: 41,259,332 (GRCm39) |
V46M |
probably damaging |
Het |
Gm3486 |
A |
T |
14: 41,206,518 (GRCm39) |
V185E |
probably benign |
Het |
Gtf3a |
C |
A |
5: 146,892,199 (GRCm39) |
R317S |
probably damaging |
Het |
Ice2 |
A |
G |
9: 69,319,510 (GRCm39) |
I320V |
probably benign |
Het |
Jag1 |
A |
G |
2: 136,957,538 (GRCm39) |
V58A |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,293,184 (GRCm39) |
E1241G |
probably benign |
Het |
Mogat2 |
T |
A |
7: 98,872,339 (GRCm39) |
I171F |
probably benign |
Het |
Muc6 |
G |
A |
7: 141,223,981 (GRCm39) |
|
probably benign |
Het |
Myo1c |
A |
T |
11: 75,549,520 (GRCm39) |
Y201F |
probably benign |
Het |
Nudt9 |
T |
C |
5: 104,209,541 (GRCm39) |
I264T |
possibly damaging |
Het |
Or8g30 |
A |
G |
9: 39,229,974 (GRCm39) |
V312A |
probably benign |
Het |
Pdcd11 |
AGAGGAGGAGGAGGAGGAGGAGGAG |
AGAGGAGGAGGAGGAGGAGGAG |
19: 47,101,876 (GRCm39) |
|
probably benign |
Het |
Rabgef1 |
T |
C |
5: 130,219,831 (GRCm39) |
V98A |
probably damaging |
Het |
Raly |
A |
G |
2: 154,707,841 (GRCm39) |
D287G |
probably damaging |
Het |
Raph1 |
A |
G |
1: 60,565,136 (GRCm39) |
V117A |
probably benign |
Het |
Slc34a2 |
T |
C |
5: 53,226,968 (GRCm39) |
F697S |
possibly damaging |
Het |
Son |
T |
A |
16: 91,453,761 (GRCm39) |
M836K |
probably damaging |
Het |
Spock1 |
T |
C |
13: 57,588,290 (GRCm39) |
M258V |
possibly damaging |
Het |
Stk10 |
G |
T |
11: 32,567,859 (GRCm39) |
C887F |
probably damaging |
Het |
Synpo2 |
A |
G |
3: 122,907,442 (GRCm39) |
S625P |
probably benign |
Het |
Synrg |
T |
A |
11: 83,900,258 (GRCm39) |
D821E |
probably damaging |
Het |
Tafa5 |
T |
C |
15: 87,604,691 (GRCm39) |
|
probably benign |
Het |
Tg |
C |
A |
15: 66,570,295 (GRCm39) |
A1389E |
possibly damaging |
Het |
Tspan33 |
G |
A |
6: 29,713,477 (GRCm39) |
V134M |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,158,960 (GRCm39) |
F2438L |
probably benign |
Het |
Vmn1r210 |
C |
T |
13: 23,011,561 (GRCm39) |
V242I |
probably benign |
Het |
Vmn1r63 |
C |
T |
7: 5,805,741 (GRCm39) |
W297* |
probably null |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Zic5 |
A |
G |
14: 122,697,073 (GRCm39) |
I514T |
unknown |
Het |
|
Other mutations in Myo9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00163:Myo9b
|
APN |
8 |
71,801,379 (GRCm39) |
missense |
probably benign |
|
IGL01020:Myo9b
|
APN |
8 |
71,804,644 (GRCm39) |
missense |
probably benign |
|
IGL01479:Myo9b
|
APN |
8 |
71,811,986 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01704:Myo9b
|
APN |
8 |
71,812,286 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01761:Myo9b
|
APN |
8 |
71,801,796 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01766:Myo9b
|
APN |
8 |
71,743,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01834:Myo9b
|
APN |
8 |
71,807,901 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01834:Myo9b
|
APN |
8 |
71,808,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01838:Myo9b
|
APN |
8 |
71,787,034 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02318:Myo9b
|
APN |
8 |
71,806,768 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02333:Myo9b
|
APN |
8 |
71,811,637 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02340:Myo9b
|
APN |
8 |
71,743,689 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02514:Myo9b
|
APN |
8 |
71,743,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02593:Myo9b
|
APN |
8 |
71,743,417 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Myo9b
|
APN |
8 |
71,807,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03332:Myo9b
|
APN |
8 |
71,801,418 (GRCm39) |
missense |
possibly damaging |
0.78 |
avantgarde
|
UTSW |
8 |
71,796,806 (GRCm39) |
missense |
probably damaging |
1.00 |
Freaky
|
UTSW |
8 |
71,743,463 (GRCm39) |
missense |
probably damaging |
1.00 |
iconoclastic
|
UTSW |
8 |
71,743,119 (GRCm39) |
missense |
probably benign |
0.37 |
unconventional
|
UTSW |
8 |
71,801,241 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4418001:Myo9b
|
UTSW |
8 |
71,775,591 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4651001:Myo9b
|
UTSW |
8 |
71,795,456 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0023:Myo9b
|
UTSW |
8 |
71,786,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R0103:Myo9b
|
UTSW |
8 |
71,776,493 (GRCm39) |
splice site |
probably benign |
|
R0103:Myo9b
|
UTSW |
8 |
71,776,493 (GRCm39) |
splice site |
probably benign |
|
R0144:Myo9b
|
UTSW |
8 |
71,798,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0207:Myo9b
|
UTSW |
8 |
71,807,869 (GRCm39) |
splice site |
probably benign |
|
R0226:Myo9b
|
UTSW |
8 |
71,806,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Myo9b
|
UTSW |
8 |
71,774,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0277:Myo9b
|
UTSW |
8 |
71,808,596 (GRCm39) |
splice site |
probably benign |
|
R0362:Myo9b
|
UTSW |
8 |
71,800,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Myo9b
|
UTSW |
8 |
71,783,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R0844:Myo9b
|
UTSW |
8 |
71,743,119 (GRCm39) |
missense |
probably benign |
0.37 |
R1051:Myo9b
|
UTSW |
8 |
71,808,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Myo9b
|
UTSW |
8 |
71,743,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Myo9b
|
UTSW |
8 |
71,743,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Myo9b
|
UTSW |
8 |
71,808,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Myo9b
|
UTSW |
8 |
71,743,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Myo9b
|
UTSW |
8 |
71,767,836 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1645:Myo9b
|
UTSW |
8 |
71,775,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Myo9b
|
UTSW |
8 |
71,806,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R1820:Myo9b
|
UTSW |
8 |
71,786,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R2037:Myo9b
|
UTSW |
8 |
71,743,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Myo9b
|
UTSW |
8 |
71,743,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Myo9b
|
UTSW |
8 |
71,812,334 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2129:Myo9b
|
UTSW |
8 |
71,786,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R2423:Myo9b
|
UTSW |
8 |
71,780,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R2869:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2869:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2871:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Myo9b
|
UTSW |
8 |
71,743,610 (GRCm39) |
missense |
probably benign |
0.01 |
R2872:Myo9b
|
UTSW |
8 |
71,743,610 (GRCm39) |
missense |
probably benign |
0.01 |
R2873:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2874:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2920:Myo9b
|
UTSW |
8 |
71,778,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R2926:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2939:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R2940:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3033:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3040:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3689:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3691:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R3735:Myo9b
|
UTSW |
8 |
71,801,241 (GRCm39) |
missense |
probably benign |
0.00 |
R4194:Myo9b
|
UTSW |
8 |
71,812,268 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4258:Myo9b
|
UTSW |
8 |
71,808,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4457:Myo9b
|
UTSW |
8 |
71,743,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R4478:Myo9b
|
UTSW |
8 |
71,743,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4496:Myo9b
|
UTSW |
8 |
71,786,981 (GRCm39) |
missense |
probably benign |
0.01 |
R4544:Myo9b
|
UTSW |
8 |
71,780,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R4580:Myo9b
|
UTSW |
8 |
71,767,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R4736:Myo9b
|
UTSW |
8 |
71,809,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5068:Myo9b
|
UTSW |
8 |
71,801,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R5124:Myo9b
|
UTSW |
8 |
71,808,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R5194:Myo9b
|
UTSW |
8 |
71,801,733 (GRCm39) |
missense |
probably benign |
0.01 |
R5296:Myo9b
|
UTSW |
8 |
71,786,032 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5528:Myo9b
|
UTSW |
8 |
71,775,918 (GRCm39) |
missense |
probably benign |
0.06 |
R5664:Myo9b
|
UTSW |
8 |
71,812,526 (GRCm39) |
missense |
probably benign |
0.13 |
R5677:Myo9b
|
UTSW |
8 |
71,796,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R5680:Myo9b
|
UTSW |
8 |
71,743,016 (GRCm39) |
missense |
probably benign |
0.00 |
R5982:Myo9b
|
UTSW |
8 |
71,801,040 (GRCm39) |
missense |
probably benign |
0.05 |
R6344:Myo9b
|
UTSW |
8 |
71,780,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R6352:Myo9b
|
UTSW |
8 |
71,801,055 (GRCm39) |
missense |
probably benign |
|
R6352:Myo9b
|
UTSW |
8 |
71,801,054 (GRCm39) |
missense |
probably benign |
0.16 |
R6411:Myo9b
|
UTSW |
8 |
71,775,599 (GRCm39) |
nonsense |
probably null |
|
R6425:Myo9b
|
UTSW |
8 |
71,786,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Myo9b
|
UTSW |
8 |
71,808,501 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6743:Myo9b
|
UTSW |
8 |
71,804,803 (GRCm39) |
splice site |
probably null |
|
R6811:Myo9b
|
UTSW |
8 |
71,809,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R6813:Myo9b
|
UTSW |
8 |
71,775,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Myo9b
|
UTSW |
8 |
71,743,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Myo9b
|
UTSW |
8 |
71,786,345 (GRCm39) |
nonsense |
probably null |
|
R7255:Myo9b
|
UTSW |
8 |
71,743,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7293:Myo9b
|
UTSW |
8 |
71,778,549 (GRCm39) |
missense |
probably benign |
0.00 |
R7342:Myo9b
|
UTSW |
8 |
71,808,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Myo9b
|
UTSW |
8 |
71,804,832 (GRCm39) |
missense |
probably benign |
0.28 |
R7482:Myo9b
|
UTSW |
8 |
71,795,442 (GRCm39) |
missense |
probably benign |
0.00 |
R7508:Myo9b
|
UTSW |
8 |
71,807,445 (GRCm39) |
missense |
probably benign |
0.00 |
R7957:Myo9b
|
UTSW |
8 |
71,807,405 (GRCm39) |
missense |
probably benign |
0.12 |
R8062:Myo9b
|
UTSW |
8 |
71,774,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R8108:Myo9b
|
UTSW |
8 |
71,800,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R8197:Myo9b
|
UTSW |
8 |
71,743,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R8274:Myo9b
|
UTSW |
8 |
71,812,480 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Myo9b
|
UTSW |
8 |
71,786,966 (GRCm39) |
missense |
probably benign |
0.01 |
R8731:Myo9b
|
UTSW |
8 |
71,806,486 (GRCm39) |
critical splice donor site |
probably null |
|
R8924:Myo9b
|
UTSW |
8 |
71,801,675 (GRCm39) |
missense |
probably benign |
|
R9056:Myo9b
|
UTSW |
8 |
71,804,906 (GRCm39) |
missense |
probably benign |
0.17 |
R9117:Myo9b
|
UTSW |
8 |
71,800,451 (GRCm39) |
missense |
probably benign |
0.03 |
R9151:Myo9b
|
UTSW |
8 |
71,807,871 (GRCm39) |
splice site |
probably benign |
|
R9315:Myo9b
|
UTSW |
8 |
71,801,811 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9332:Myo9b
|
UTSW |
8 |
71,812,246 (GRCm39) |
missense |
probably benign |
0.07 |
R9364:Myo9b
|
UTSW |
8 |
71,808,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R9569:Myo9b
|
UTSW |
8 |
71,811,629 (GRCm39) |
missense |
probably benign |
|
R9581:Myo9b
|
UTSW |
8 |
71,812,543 (GRCm39) |
missense |
probably benign |
0.19 |
R9600:Myo9b
|
UTSW |
8 |
71,743,075 (GRCm39) |
missense |
possibly damaging |
0.80 |
X0066:Myo9b
|
UTSW |
8 |
71,776,542 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Myo9b
|
UTSW |
8 |
71,743,353 (GRCm39) |
missense |
probably damaging |
1.00 |
|