Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akt2 |
T |
A |
7: 27,328,824 (GRCm39) |
I182N |
probably damaging |
Het |
Alpk3 |
A |
G |
7: 80,728,255 (GRCm39) |
T462A |
probably benign |
Het |
Amz1 |
A |
G |
5: 140,738,014 (GRCm39) |
R425G |
probably damaging |
Het |
Aoc2 |
A |
G |
11: 101,217,201 (GRCm39) |
E428G |
probably damaging |
Het |
Car4 |
C |
T |
11: 84,856,593 (GRCm39) |
P294S |
probably damaging |
Het |
Chchd6 |
A |
T |
6: 89,396,762 (GRCm39) |
H216Q |
probably damaging |
Het |
Chl1 |
A |
G |
6: 103,675,086 (GRCm39) |
Y591C |
probably damaging |
Het |
Cln8 |
T |
C |
8: 14,945,178 (GRCm39) |
L164S |
probably damaging |
Het |
Dscaml1 |
T |
C |
9: 45,581,474 (GRCm39) |
I431T |
possibly damaging |
Het |
Fam234b |
T |
C |
6: 135,208,659 (GRCm39) |
L524P |
probably damaging |
Het |
Fmo1 |
T |
C |
1: 162,660,559 (GRCm39) |
N410S |
probably benign |
Het |
Ftsj3 |
G |
A |
11: 106,143,972 (GRCm39) |
R251* |
probably null |
Het |
Greb1l |
A |
T |
18: 10,515,200 (GRCm39) |
D555V |
probably damaging |
Het |
Hcar1 |
G |
T |
5: 124,017,135 (GRCm39) |
H185Q |
probably damaging |
Het |
Kcnj12 |
G |
A |
11: 60,960,319 (GRCm39) |
V206I |
probably benign |
Het |
Lamc3 |
G |
A |
2: 31,808,469 (GRCm39) |
G742S |
probably damaging |
Het |
Lipg |
T |
C |
18: 75,093,946 (GRCm39) |
|
probably null |
Het |
Ltbp2 |
A |
G |
12: 84,839,729 (GRCm39) |
|
probably null |
Het |
Mcm3ap |
T |
G |
10: 76,332,386 (GRCm39) |
Y1234* |
probably null |
Het |
Myh6 |
T |
A |
14: 55,194,612 (GRCm39) |
D719V |
possibly damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,858 (GRCm39) |
E270G |
probably benign |
Het |
Notch2 |
G |
A |
3: 98,054,652 (GRCm39) |
W2438* |
probably null |
Het |
Nphp1 |
G |
A |
2: 127,621,987 (GRCm39) |
Q47* |
probably null |
Het |
Nptx2 |
T |
C |
5: 144,493,056 (GRCm39) |
L381P |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,402 (GRCm39) |
N911S |
possibly damaging |
Het |
Or10j2 |
A |
T |
1: 173,097,972 (GRCm39) |
I77F |
probably benign |
Het |
Or5d46 |
T |
C |
2: 88,169,906 (GRCm39) |
|
probably benign |
Het |
P4ha1 |
T |
A |
10: 59,188,023 (GRCm39) |
F260Y |
probably benign |
Het |
Pitpnm2 |
T |
C |
5: 124,268,676 (GRCm39) |
D504G |
probably damaging |
Het |
Prss54 |
A |
G |
8: 96,292,237 (GRCm39) |
V114A |
probably benign |
Het |
Ptprc |
G |
A |
1: 137,998,957 (GRCm39) |
T1031M |
probably damaging |
Het |
Rtf2 |
T |
C |
2: 172,310,511 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
A |
G |
2: 112,777,349 (GRCm39) |
|
probably benign |
Het |
Slc14a2 |
C |
T |
18: 78,206,341 (GRCm39) |
E492K |
probably damaging |
Het |
Stab1 |
G |
T |
14: 30,862,367 (GRCm39) |
N2322K |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 130,087,369 (GRCm39) |
N1162S |
probably benign |
Het |
Tmprss11b |
T |
C |
5: 86,810,090 (GRCm39) |
I297V |
probably benign |
Het |
Tnn |
T |
C |
1: 159,972,775 (GRCm39) |
N276D |
probably benign |
Het |
Trhde |
A |
T |
10: 114,428,118 (GRCm39) |
|
probably benign |
Het |
Vmn1r115 |
T |
A |
7: 20,578,453 (GRCm39) |
H153L |
possibly damaging |
Het |
Vmn1r203 |
T |
A |
13: 22,708,997 (GRCm39) |
C259* |
probably null |
Het |
Xpot |
T |
A |
10: 121,451,109 (GRCm39) |
E97V |
probably damaging |
Het |
Zbtb2 |
T |
C |
10: 4,318,712 (GRCm39) |
D438G |
probably damaging |
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 |
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 |
R0227:Myo9b
|
UTSW |
8 |
71,796,806 (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 |
|