Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013G24Rik |
T |
G |
4: 137,454,579 (GRCm38) |
L15W |
probably damaging |
Het |
4930550C14Rik |
G |
A |
9: 53,411,756 (GRCm38) |
V31I |
possibly damaging |
Het |
4932415D10Rik |
T |
C |
10: 82,291,899 (GRCm38) |
D1759G |
possibly damaging |
Het |
Adgre1 |
C |
T |
17: 57,408,445 (GRCm38) |
S255F |
probably benign |
Het |
Aff4 |
T |
G |
11: 53,398,237 (GRCm38) |
S404R |
probably damaging |
Het |
Akr1c19 |
A |
T |
13: 4,233,758 (GRCm38) |
|
probably benign |
Het |
Ankrd31 |
T |
A |
13: 96,878,249 (GRCm38) |
I1342K |
probably damaging |
Het |
Arhgap5 |
T |
A |
12: 52,518,125 (GRCm38) |
D626E |
possibly damaging |
Het |
Arhgef1 |
G |
A |
7: 24,916,923 (GRCm38) |
V332I |
probably benign |
Het |
AY358078 |
A |
G |
14: 51,826,187 (GRCm38) |
E430G |
probably damaging |
Het |
B4gat1 |
T |
A |
19: 5,040,434 (GRCm38) |
I395N |
probably benign |
Het |
Bub1b |
T |
A |
2: 118,636,830 (GRCm38) |
I878N |
probably damaging |
Het |
Ccdc150 |
C |
T |
1: 54,355,709 (GRCm38) |
Q745* |
probably null |
Het |
Ccl19 |
A |
T |
4: 42,754,885 (GRCm38) |
I87N |
probably damaging |
Het |
Ces2g |
G |
C |
8: 104,963,908 (GRCm38) |
G107A |
probably benign |
Het |
Chpt1 |
A |
G |
10: 88,488,406 (GRCm38) |
V180A |
probably damaging |
Het |
Col2a1 |
T |
C |
15: 98,004,454 (GRCm38) |
T14A |
unknown |
Het |
Dnah7a |
T |
C |
1: 53,582,625 (GRCm38) |
I1114V |
possibly damaging |
Het |
Dnah7c |
T |
C |
1: 46,666,213 (GRCm38) |
I2462T |
possibly damaging |
Het |
Dnah8 |
T |
C |
17: 30,643,275 (GRCm38) |
F208S |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,714,210 (GRCm38) |
E3993G |
probably damaging |
Het |
Erv3 |
C |
T |
2: 131,855,966 (GRCm38) |
D158N |
possibly damaging |
Het |
Exoc6 |
T |
A |
19: 37,609,091 (GRCm38) |
F647I |
probably damaging |
Het |
Fbrs |
G |
A |
7: 127,479,508 (GRCm38) |
|
probably benign |
Het |
Fgfr1op2 |
T |
C |
6: 146,589,965 (GRCm38) |
F109L |
probably damaging |
Het |
Fv1 |
T |
C |
4: 147,869,271 (GRCm38) |
F98S |
possibly damaging |
Het |
Gm436 |
A |
G |
4: 144,686,325 (GRCm38) |
F15S |
probably benign |
Het |
H2-M10.1 |
T |
C |
17: 36,325,592 (GRCm38) |
K107E |
probably benign |
Het |
Hspg2 |
A |
T |
4: 137,528,890 (GRCm38) |
Q1436L |
probably damaging |
Het |
Ighv1-74 |
T |
C |
12: 115,802,763 (GRCm38) |
Y79C |
probably damaging |
Het |
Kcnj1 |
G |
A |
9: 32,396,585 (GRCm38) |
V102I |
probably benign |
Het |
Mnt |
C |
A |
11: 74,842,809 (GRCm38) |
|
probably benign |
Het |
Mrpl15 |
T |
C |
1: 4,782,660 (GRCm38) |
T112A |
probably benign |
Het |
Ncdn |
T |
C |
4: 126,747,189 (GRCm38) |
D506G |
probably benign |
Het |
Ogdh |
C |
T |
11: 6,313,806 (GRCm38) |
R81* |
probably null |
Het |
Olfr791 |
T |
A |
10: 129,526,673 (GRCm38) |
S149T |
probably benign |
Het |
Olfr815 |
G |
C |
10: 129,902,409 (GRCm38) |
F100L |
probably damaging |
Het |
Pole |
G |
T |
5: 110,329,583 (GRCm38) |
V1863F |
probably damaging |
Het |
Pramel5 |
T |
C |
4: 144,274,007 (GRCm38) |
|
probably benign |
Het |
Rabep1 |
A |
G |
11: 70,934,537 (GRCm38) |
K636E |
probably damaging |
Het |
Rasgrf2 |
T |
A |
13: 91,885,635 (GRCm38) |
Y1151F |
probably benign |
Het |
Rrad |
A |
G |
8: 104,630,636 (GRCm38) |
V93A |
probably damaging |
Het |
Sesn3 |
A |
T |
9: 14,310,257 (GRCm38) |
R118* |
probably null |
Het |
Slc27a3 |
T |
C |
3: 90,386,290 (GRCm38) |
N596S |
probably benign |
Het |
Snx19 |
C |
A |
9: 30,428,935 (GRCm38) |
D456E |
probably damaging |
Het |
Supt20 |
T |
C |
3: 54,698,597 (GRCm38) |
S35P |
probably damaging |
Het |
Syde2 |
G |
T |
3: 146,019,809 (GRCm38) |
R885L |
probably benign |
Het |
Synm |
G |
A |
7: 67,733,658 (GRCm38) |
L1419F |
probably damaging |
Het |
Tcrg-V6 |
G |
T |
13: 19,190,644 (GRCm38) |
G40W |
possibly damaging |
Het |
Tekt2 |
A |
G |
4: 126,323,443 (GRCm38) |
F221L |
probably benign |
Het |
Ticam1 |
C |
T |
17: 56,269,900 (GRCm38) |
E732K |
probably benign |
Het |
Tmem39b |
A |
G |
4: 129,693,148 (GRCm38) |
I90T |
possibly damaging |
Het |
Trib2 |
A |
G |
12: 15,815,338 (GRCm38) |
S79P |
probably damaging |
Het |
Vmn1r181 |
T |
C |
7: 23,984,847 (GRCm38) |
F246L |
probably damaging |
Het |
Wnt16 |
A |
G |
6: 22,288,511 (GRCm38) |
D2G |
probably damaging |
Het |
Zfp462 |
A |
G |
4: 55,080,716 (GRCm38) |
E1357G |
probably benign |
Het |
Zhx3 |
A |
G |
2: 160,779,868 (GRCm38) |
M793T |
probably benign |
Het |
|
Other mutations in Usp32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00529:Usp32
|
APN |
11 |
84,994,426 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00701:Usp32
|
APN |
11 |
85,059,125 (GRCm38) |
splice site |
probably null |
|
IGL00848:Usp32
|
APN |
11 |
85,051,181 (GRCm38) |
splice site |
probably benign |
|
IGL00934:Usp32
|
APN |
11 |
85,007,076 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01019:Usp32
|
APN |
11 |
85,039,265 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01302:Usp32
|
APN |
11 |
84,988,482 (GRCm38) |
missense |
probably benign |
0.05 |
IGL01444:Usp32
|
APN |
11 |
85,059,164 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01575:Usp32
|
APN |
11 |
85,022,802 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01981:Usp32
|
APN |
11 |
85,036,524 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02118:Usp32
|
APN |
11 |
85,032,177 (GRCm38) |
nonsense |
probably null |
|
IGL02159:Usp32
|
APN |
11 |
85,005,802 (GRCm38) |
splice site |
probably null |
|
IGL02227:Usp32
|
APN |
11 |
84,986,481 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02363:Usp32
|
APN |
11 |
85,044,787 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02524:Usp32
|
APN |
11 |
85,010,011 (GRCm38) |
nonsense |
probably null |
|
IGL02613:Usp32
|
APN |
11 |
85,040,070 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02720:Usp32
|
APN |
11 |
85,006,991 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02738:Usp32
|
APN |
11 |
85,083,806 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02929:Usp32
|
APN |
11 |
84,988,372 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03303:Usp32
|
APN |
11 |
85,022,832 (GRCm38) |
missense |
probably damaging |
1.00 |
BB010:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
BB020:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4812001:Usp32
|
UTSW |
11 |
85,010,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R0026:Usp32
|
UTSW |
11 |
85,032,074 (GRCm38) |
missense |
possibly damaging |
0.48 |
R0295:Usp32
|
UTSW |
11 |
85,053,692 (GRCm38) |
missense |
probably damaging |
0.98 |
R1320:Usp32
|
UTSW |
11 |
85,017,793 (GRCm38) |
missense |
probably damaging |
0.98 |
R1712:Usp32
|
UTSW |
11 |
85,042,580 (GRCm38) |
missense |
probably benign |
0.12 |
R1922:Usp32
|
UTSW |
11 |
85,007,004 (GRCm38) |
nonsense |
probably null |
|
R1973:Usp32
|
UTSW |
11 |
85,103,931 (GRCm38) |
missense |
probably benign |
0.09 |
R2010:Usp32
|
UTSW |
11 |
85,040,004 (GRCm38) |
missense |
probably damaging |
0.98 |
R2082:Usp32
|
UTSW |
11 |
85,030,512 (GRCm38) |
missense |
probably damaging |
0.99 |
R2355:Usp32
|
UTSW |
11 |
85,005,909 (GRCm38) |
missense |
probably benign |
0.34 |
R3147:Usp32
|
UTSW |
11 |
85,029,087 (GRCm38) |
missense |
probably damaging |
1.00 |
R3160:Usp32
|
UTSW |
11 |
85,025,536 (GRCm38) |
missense |
probably damaging |
0.97 |
R3162:Usp32
|
UTSW |
11 |
85,025,536 (GRCm38) |
missense |
probably damaging |
0.97 |
R3716:Usp32
|
UTSW |
11 |
85,042,563 (GRCm38) |
missense |
probably damaging |
1.00 |
R3816:Usp32
|
UTSW |
11 |
84,994,384 (GRCm38) |
critical splice donor site |
probably null |
|
R3870:Usp32
|
UTSW |
11 |
85,007,055 (GRCm38) |
nonsense |
probably null |
|
R3871:Usp32
|
UTSW |
11 |
85,081,156 (GRCm38) |
missense |
probably null |
0.81 |
R4041:Usp32
|
UTSW |
11 |
85,017,739 (GRCm38) |
missense |
probably benign |
0.40 |
R4079:Usp32
|
UTSW |
11 |
85,039,229 (GRCm38) |
missense |
probably damaging |
0.98 |
R4332:Usp32
|
UTSW |
11 |
85,103,978 (GRCm38) |
missense |
possibly damaging |
0.79 |
R4396:Usp32
|
UTSW |
11 |
85,053,975 (GRCm38) |
missense |
probably benign |
|
R4580:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably null |
|
R4620:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably null |
|
R4744:Usp32
|
UTSW |
11 |
84,994,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R4909:Usp32
|
UTSW |
11 |
85,055,772 (GRCm38) |
nonsense |
probably null |
|
R5056:Usp32
|
UTSW |
11 |
85,026,795 (GRCm38) |
missense |
probably benign |
0.07 |
R5111:Usp32
|
UTSW |
11 |
85,077,331 (GRCm38) |
missense |
possibly damaging |
0.95 |
R5213:Usp32
|
UTSW |
11 |
85,022,259 (GRCm38) |
missense |
probably damaging |
1.00 |
R5308:Usp32
|
UTSW |
11 |
85,017,718 (GRCm38) |
missense |
probably benign |
0.12 |
R5381:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably benign |
|
R5538:Usp32
|
UTSW |
11 |
85,017,786 (GRCm38) |
missense |
possibly damaging |
0.65 |
R5659:Usp32
|
UTSW |
11 |
85,077,414 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6006:Usp32
|
UTSW |
11 |
84,992,451 (GRCm38) |
critical splice donor site |
probably null |
|
R6011:Usp32
|
UTSW |
11 |
85,032,097 (GRCm38) |
missense |
possibly damaging |
0.70 |
R6029:Usp32
|
UTSW |
11 |
85,025,582 (GRCm38) |
missense |
probably damaging |
0.99 |
R6074:Usp32
|
UTSW |
11 |
84,994,573 (GRCm38) |
missense |
probably benign |
0.00 |
R6331:Usp32
|
UTSW |
11 |
84,986,576 (GRCm38) |
missense |
possibly damaging |
0.92 |
R6353:Usp32
|
UTSW |
11 |
85,022,281 (GRCm38) |
missense |
probably benign |
|
R6714:Usp32
|
UTSW |
11 |
85,026,870 (GRCm38) |
missense |
probably damaging |
0.99 |
R6778:Usp32
|
UTSW |
11 |
85,025,686 (GRCm38) |
missense |
probably benign |
0.00 |
R6992:Usp32
|
UTSW |
11 |
85,032,088 (GRCm38) |
missense |
probably damaging |
0.99 |
R7182:Usp32
|
UTSW |
11 |
85,040,170 (GRCm38) |
missense |
probably benign |
0.34 |
R7186:Usp32
|
UTSW |
11 |
85,051,234 (GRCm38) |
missense |
probably benign |
0.45 |
R7198:Usp32
|
UTSW |
11 |
85,022,855 (GRCm38) |
frame shift |
probably null |
|
R7201:Usp32
|
UTSW |
11 |
85,022,855 (GRCm38) |
frame shift |
probably null |
|
R7469:Usp32
|
UTSW |
11 |
84,988,553 (GRCm38) |
missense |
possibly damaging |
0.94 |
R7502:Usp32
|
UTSW |
11 |
85,022,898 (GRCm38) |
missense |
possibly damaging |
0.48 |
R7513:Usp32
|
UTSW |
11 |
85,027,112 (GRCm38) |
nonsense |
probably null |
|
R7629:Usp32
|
UTSW |
11 |
85,019,855 (GRCm38) |
frame shift |
probably null |
|
R7703:Usp32
|
UTSW |
11 |
85,077,327 (GRCm38) |
missense |
probably damaging |
0.99 |
R7741:Usp32
|
UTSW |
11 |
84,987,281 (GRCm38) |
missense |
probably damaging |
0.99 |
R7765:Usp32
|
UTSW |
11 |
84,994,408 (GRCm38) |
missense |
probably damaging |
1.00 |
R7933:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
R7973:Usp32
|
UTSW |
11 |
85,022,808 (GRCm38) |
missense |
probably damaging |
0.99 |
R7989:Usp32
|
UTSW |
11 |
85,034,300 (GRCm38) |
missense |
|
|
R7998:Usp32
|
UTSW |
11 |
84,994,426 (GRCm38) |
missense |
probably damaging |
1.00 |
R8292:Usp32
|
UTSW |
11 |
85,077,401 (GRCm38) |
missense |
probably damaging |
0.99 |
R8305:Usp32
|
UTSW |
11 |
85,032,185 (GRCm38) |
missense |
possibly damaging |
0.83 |
R8548:Usp32
|
UTSW |
11 |
85,017,827 (GRCm38) |
missense |
possibly damaging |
0.52 |
R8924:Usp32
|
UTSW |
11 |
85,025,544 (GRCm38) |
missense |
probably damaging |
0.98 |
R9002:Usp32
|
UTSW |
11 |
85,053,951 (GRCm38) |
missense |
probably damaging |
0.96 |
R9145:Usp32
|
UTSW |
11 |
85,022,292 (GRCm38) |
missense |
probably damaging |
1.00 |
R9209:Usp32
|
UTSW |
11 |
85,040,012 (GRCm38) |
missense |
probably damaging |
0.98 |
R9211:Usp32
|
UTSW |
11 |
85,022,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R9296:Usp32
|
UTSW |
11 |
85,017,652 (GRCm38) |
missense |
probably damaging |
1.00 |
R9310:Usp32
|
UTSW |
11 |
85,051,202 (GRCm38) |
missense |
probably benign |
0.29 |
R9417:Usp32
|
UTSW |
11 |
84,994,543 (GRCm38) |
missense |
probably damaging |
1.00 |
R9514:Usp32
|
UTSW |
11 |
85,022,734 (GRCm38) |
missense |
probably damaging |
0.99 |
R9652:Usp32
|
UTSW |
11 |
85,030,491 (GRCm38) |
missense |
probably damaging |
0.97 |
R9723:Usp32
|
UTSW |
11 |
85,044,710 (GRCm38) |
nonsense |
probably null |
|
R9757:Usp32
|
UTSW |
11 |
85,077,329 (GRCm38) |
nonsense |
probably null |
|
X0028:Usp32
|
UTSW |
11 |
84,992,606 (GRCm38) |
missense |
probably benign |
0.05 |
Z1177:Usp32
|
UTSW |
11 |
84,988,612 (GRCm38) |
nonsense |
probably null |
|
|