Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aarsd1 |
T |
G |
11: 101,308,018 (GRCm39) |
T28P |
probably benign |
Het |
Abcc1 |
C |
A |
16: 14,283,033 (GRCm39) |
R1170S |
probably damaging |
Het |
Adam8 |
T |
C |
7: 139,566,304 (GRCm39) |
N568S |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,926,467 (GRCm39) |
R65G |
probably damaging |
Het |
Arid4b |
A |
C |
13: 14,310,804 (GRCm39) |
I136L |
probably benign |
Het |
Ash1l |
G |
T |
3: 88,873,304 (GRCm39) |
G29V |
possibly damaging |
Het |
Atp6v0a2 |
A |
G |
5: 124,784,676 (GRCm39) |
T320A |
probably damaging |
Het |
B4gat1 |
G |
A |
19: 5,089,686 (GRCm39) |
V228M |
probably benign |
Het |
Calcr |
T |
A |
6: 3,691,536 (GRCm39) |
H450L |
probably benign |
Het |
Cand1 |
A |
T |
10: 119,047,692 (GRCm39) |
N599K |
possibly damaging |
Het |
Cblif |
A |
T |
19: 11,740,587 (GRCm39) |
H407L |
probably benign |
Het |
Cel |
A |
T |
2: 28,450,649 (GRCm39) |
Y125* |
probably null |
Het |
Cfi |
T |
A |
3: 129,668,781 (GRCm39) |
N602K |
probably damaging |
Het |
Clstn1 |
G |
A |
4: 149,713,887 (GRCm39) |
A190T |
probably damaging |
Het |
Cmklr1 |
C |
T |
5: 113,752,354 (GRCm39) |
V216M |
probably benign |
Het |
Cntnap5a |
A |
G |
1: 115,987,852 (GRCm39) |
T128A |
probably benign |
Het |
Creld2 |
A |
G |
15: 88,710,610 (GRCm39) |
T342A |
probably benign |
Het |
Ctbp2 |
T |
C |
7: 132,616,041 (GRCm39) |
E298G |
probably damaging |
Het |
Ctsh |
A |
T |
9: 89,957,040 (GRCm39) |
E307V |
probably benign |
Het |
Cxcl10 |
T |
A |
5: 92,496,029 (GRCm39) |
D36V |
probably benign |
Het |
Dgkb |
A |
G |
12: 38,150,432 (GRCm39) |
T73A |
probably benign |
Het |
Dnah3 |
T |
G |
7: 119,629,208 (GRCm39) |
E1449A |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,919,552 (GRCm39) |
M683T |
probably benign |
Het |
Foxn4 |
C |
A |
5: 114,396,760 (GRCm39) |
W241L |
probably damaging |
Het |
Gosr1 |
T |
C |
11: 76,621,033 (GRCm39) |
I219V |
probably benign |
Het |
Gtf2f2 |
T |
C |
14: 76,144,317 (GRCm39) |
D179G |
probably damaging |
Het |
Ighg2b |
A |
G |
12: 113,270,050 (GRCm39) |
Y323H |
|
Het |
Itpr2 |
A |
T |
6: 146,228,685 (GRCm39) |
H1303Q |
probably damaging |
Het |
Kif1b |
A |
C |
4: 149,298,547 (GRCm39) |
Y1040D |
possibly damaging |
Het |
Lbr |
C |
T |
1: 181,653,186 (GRCm39) |
|
probably null |
Het |
Lrp2 |
A |
G |
2: 69,309,634 (GRCm39) |
V2755A |
possibly damaging |
Het |
Lrp6 |
G |
T |
6: 134,427,781 (GRCm39) |
P1604T |
probably damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,619,431 (GRCm39) |
C606S |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,275,917 (GRCm39) |
E6217G |
probably damaging |
Het |
Ms4a6d |
G |
A |
19: 11,567,437 (GRCm39) |
Q155* |
probably null |
Het |
Naip2 |
A |
T |
13: 100,325,864 (GRCm39) |
F15I |
probably benign |
Het |
Neb |
A |
T |
2: 52,171,679 (GRCm39) |
S1605T |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,210,831 (GRCm39) |
E419G |
probably damaging |
Het |
Or14a260 |
G |
A |
7: 85,985,295 (GRCm39) |
T103I |
probably benign |
Het |
Or8c18 |
A |
G |
9: 38,203,574 (GRCm39) |
Y111C |
probably damaging |
Het |
Paip2b |
T |
A |
6: 83,791,808 (GRCm39) |
S25C |
probably damaging |
Het |
Pgbd5 |
G |
A |
8: 125,160,709 (GRCm39) |
R53C |
probably benign |
Het |
Plin4 |
T |
C |
17: 56,411,608 (GRCm39) |
T808A |
probably benign |
Het |
Pramel11 |
A |
T |
4: 143,623,520 (GRCm39) |
I218K |
probably benign |
Het |
Prex2 |
A |
G |
1: 11,232,549 (GRCm39) |
D872G |
probably benign |
Het |
Ptf1a |
A |
G |
2: 19,451,977 (GRCm39) |
*325W |
probably null |
Het |
Ptprg |
T |
C |
14: 12,237,151 (GRCm38) |
V1390A |
possibly damaging |
Het |
Rhpn2 |
A |
G |
7: 35,033,771 (GRCm39) |
T2A |
probably damaging |
Het |
Rpl18a |
T |
C |
8: 71,348,042 (GRCm39) |
N214D |
unknown |
Het |
Scp2 |
T |
A |
4: 107,948,518 (GRCm39) |
Y197F |
probably benign |
Het |
Sftpb |
G |
A |
6: 72,286,858 (GRCm39) |
R254H |
probably benign |
Het |
Slc17a9 |
T |
C |
2: 180,378,555 (GRCm39) |
L246P |
probably damaging |
Het |
Slc38a9 |
G |
T |
13: 112,806,125 (GRCm39) |
|
probably benign |
Het |
Slc4a1ap |
C |
T |
5: 31,693,634 (GRCm39) |
L523F |
possibly damaging |
Het |
Spats2l |
C |
A |
1: 57,925,106 (GRCm39) |
T168K |
possibly damaging |
Het |
Sstr1 |
A |
G |
12: 58,260,456 (GRCm39) |
S360G |
possibly damaging |
Het |
Taf1b |
A |
T |
12: 24,608,343 (GRCm39) |
K581* |
probably null |
Het |
Tfip11 |
T |
A |
5: 112,475,838 (GRCm39) |
M1K |
probably null |
Het |
Tgoln1 |
G |
C |
6: 72,593,261 (GRCm39) |
T73R |
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,551,583 (GRCm39) |
H48Y |
probably benign |
Het |
Uggt2 |
T |
A |
14: 119,232,384 (GRCm39) |
H1489L |
possibly damaging |
Het |
Unc13b |
T |
C |
4: 43,258,703 (GRCm39) |
L1346P |
probably damaging |
Het |
Vmac |
T |
C |
17: 57,022,644 (GRCm39) |
E122G |
probably benign |
Het |
Vmn2r125 |
T |
C |
4: 156,703,138 (GRCm39) |
V172A |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,648,014 (GRCm39) |
|
probably benign |
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 |
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 |
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 |
|