Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca5 |
A |
G |
11: 110,188,908 (GRCm39) |
F850L |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,411 (GRCm39) |
D627E |
probably damaging |
Het |
Add2 |
C |
A |
6: 86,081,459 (GRCm39) |
|
probably benign |
Het |
Anpep |
T |
C |
7: 79,491,785 (GRCm39) |
N72S |
probably benign |
Het |
Aqp6 |
A |
G |
15: 99,501,655 (GRCm39) |
T238A |
possibly damaging |
Het |
Arhgef38 |
G |
T |
3: 132,912,706 (GRCm39) |
T111K |
|
Het |
Atg10 |
A |
G |
13: 91,189,032 (GRCm39) |
Y93H |
probably damaging |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cald1 |
A |
G |
6: 34,732,682 (GRCm39) |
N286S |
unknown |
Het |
Caps2 |
A |
T |
10: 112,031,829 (GRCm39) |
I322F |
possibly damaging |
Het |
Cbx3 |
T |
A |
6: 51,455,533 (GRCm39) |
S95T |
probably benign |
Het |
Ccdc24 |
T |
C |
4: 117,727,102 (GRCm39) |
T83A |
unknown |
Het |
Cntn1 |
T |
C |
15: 92,140,864 (GRCm39) |
Y197H |
probably damaging |
Het |
Cpd |
A |
G |
11: 76,675,275 (GRCm39) |
I1282T |
possibly damaging |
Het |
Crat |
A |
T |
2: 30,295,052 (GRCm39) |
S454R |
probably damaging |
Het |
D2hgdh |
G |
A |
1: 93,754,338 (GRCm39) |
V126I |
probably benign |
Het |
Dcst1 |
A |
G |
3: 89,271,558 (GRCm39) |
V75A |
probably benign |
Het |
Dnm1l |
T |
C |
16: 16,176,668 (GRCm39) |
D21G |
probably benign |
Het |
Evc2 |
A |
G |
5: 37,504,823 (GRCm39) |
N74D |
probably benign |
Het |
Gm19965 |
A |
T |
1: 116,748,942 (GRCm39) |
M208L |
|
Het |
Gprc6a |
T |
G |
10: 51,497,182 (GRCm39) |
T454P |
possibly damaging |
Het |
Gprin1 |
C |
T |
13: 54,886,778 (GRCm39) |
V499M |
probably benign |
Het |
Gtf3c5 |
A |
G |
2: 28,463,577 (GRCm39) |
Y194H |
probably damaging |
Het |
Hcn4 |
T |
C |
9: 58,767,880 (GRCm39) |
V1147A |
possibly damaging |
Het |
Ighv1-82 |
A |
C |
12: 115,916,342 (GRCm39) |
V56G |
probably damaging |
Het |
Ins2 |
T |
C |
7: 142,232,505 (GRCm39) |
D93G |
possibly damaging |
Het |
Itgb8 |
A |
G |
12: 119,130,535 (GRCm39) |
S658P |
probably benign |
Het |
Kcnmb1 |
T |
C |
11: 33,920,263 (GRCm39) |
F159L |
probably benign |
Het |
Klf1 |
C |
T |
8: 85,629,954 (GRCm39) |
L260F |
probably benign |
Het |
Larp4 |
T |
A |
15: 99,888,205 (GRCm39) |
S140T |
possibly damaging |
Het |
Maneal |
C |
A |
4: 124,755,542 (GRCm39) |
R140L |
probably benign |
Het |
Mfsd11 |
T |
A |
11: 116,750,323 (GRCm39) |
V114D |
|
Het |
Muc4 |
A |
G |
16: 32,752,617 (GRCm38) |
T832A |
probably benign |
Het |
Myh11 |
T |
G |
16: 14,050,439 (GRCm39) |
I509L |
|
Het |
Myh13 |
A |
T |
11: 67,252,149 (GRCm39) |
E1419V |
probably damaging |
Het |
Myh7b |
A |
G |
2: 155,474,439 (GRCm39) |
E1718G |
probably damaging |
Het |
Notch1 |
A |
T |
2: 26,367,939 (GRCm39) |
L656Q |
probably benign |
Het |
Nova1 |
A |
G |
12: 46,746,813 (GRCm39) |
I488T |
probably damaging |
Het |
Or51r1 |
A |
T |
7: 102,228,500 (GRCm39) |
E266V |
probably damaging |
Het |
Or5b113 |
A |
T |
19: 13,342,222 (GRCm39) |
T77S |
possibly damaging |
Het |
Or5b21 |
A |
G |
19: 12,839,976 (GRCm39) |
Y279C |
probably damaging |
Het |
Or5d18 |
A |
G |
2: 87,864,697 (GRCm39) |
V262A |
probably damaging |
Het |
Or6c35 |
A |
G |
10: 129,169,623 (GRCm39) |
N291S |
probably damaging |
Het |
Or6d13 |
A |
T |
6: 116,517,990 (GRCm39) |
N192I |
possibly damaging |
Het |
Pax6 |
C |
T |
2: 105,523,097 (GRCm39) |
S325L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,619,740 (GRCm39) |
D142G |
probably null |
Het |
Phldb3 |
T |
G |
7: 24,324,048 (GRCm39) |
|
probably benign |
Het |
Pikfyve |
G |
T |
1: 65,235,898 (GRCm39) |
R190L |
probably damaging |
Het |
Plagl2 |
A |
T |
2: 153,074,540 (GRCm39) |
H120Q |
probably damaging |
Het |
Pou2f1 |
A |
T |
1: 165,703,640 (GRCm39) |
|
probably benign |
Het |
Pramel58 |
A |
G |
5: 94,831,836 (GRCm39) |
Y281C |
possibly damaging |
Het |
Prpf6 |
A |
G |
2: 181,250,001 (GRCm39) |
R54G |
possibly damaging |
Het |
Prss33 |
T |
C |
17: 24,052,966 (GRCm39) |
E236G |
probably benign |
Het |
Ptpru |
T |
C |
4: 131,522,278 (GRCm39) |
Y709C |
probably benign |
Het |
Rcc1l |
A |
G |
5: 134,197,057 (GRCm39) |
V212A |
probably benign |
Het |
Rtl1 |
G |
A |
12: 109,560,007 (GRCm39) |
L611F |
|
Het |
Scp2 |
A |
G |
4: 107,931,603 (GRCm39) |
I344T |
possibly damaging |
Het |
Serpinb2 |
A |
T |
1: 107,449,890 (GRCm39) |
D101V |
possibly damaging |
Het |
Slc13a1 |
T |
C |
6: 24,097,662 (GRCm39) |
T422A |
probably damaging |
Het |
Slc38a10 |
G |
T |
11: 120,007,762 (GRCm39) |
T406K |
probably benign |
Het |
Smad4 |
T |
C |
18: 73,782,806 (GRCm39) |
E376G |
probably damaging |
Het |
Smarcb1 |
T |
C |
10: 75,750,916 (GRCm39) |
E115G |
probably benign |
Het |
Spata31h1 |
A |
T |
10: 82,120,928 (GRCm39) |
H4027Q |
probably damaging |
Het |
Taf5 |
G |
A |
19: 47,063,370 (GRCm39) |
V307I |
probably damaging |
Het |
Tnc |
T |
C |
4: 63,938,686 (GRCm39) |
N51S |
possibly damaging |
Het |
Trp53inp2 |
G |
T |
2: 155,228,558 (GRCm39) |
R171L |
possibly damaging |
Het |
Ttc13 |
A |
T |
8: 125,402,021 (GRCm39) |
D579E |
probably benign |
Het |
Ttn |
A |
T |
2: 76,775,896 (GRCm39) |
N1761K |
unknown |
Het |
Ttpa |
C |
T |
4: 20,008,401 (GRCm39) |
|
probably benign |
Het |
Ugt3a1 |
G |
A |
15: 9,362,051 (GRCm39) |
V276I |
probably benign |
Het |
Usp4 |
T |
A |
9: 108,244,011 (GRCm39) |
H296Q |
probably benign |
Het |
Vmn1r119 |
T |
A |
7: 20,745,593 (GRCm39) |
H263L |
possibly damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,103,905 (GRCm39) |
D176G |
|
Het |
Wdr1 |
A |
T |
5: 38,687,468 (GRCm39) |
|
probably benign |
Het |
Zfp488 |
T |
G |
14: 33,692,695 (GRCm39) |
Q156P |
possibly 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 |
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 |
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 |
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 |
|