Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
A |
T |
15: 64,743,625 (GRCm39) |
C328S |
probably benign |
Het |
Adgrv1 |
G |
T |
13: 81,572,407 (GRCm39) |
T4918K |
probably benign |
Het |
Aen |
T |
C |
7: 78,555,660 (GRCm39) |
Y108H |
probably damaging |
Het |
Amer3 |
T |
C |
1: 34,627,252 (GRCm39) |
M497T |
probably damaging |
Het |
Arid2 |
C |
T |
15: 96,269,535 (GRCm39) |
T1216M |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,916,404 (GRCm39) |
|
probably null |
Het |
Bzw2 |
A |
G |
12: 36,169,126 (GRCm39) |
|
probably benign |
Het |
Ccr1 |
T |
C |
9: 123,763,573 (GRCm39) |
H319R |
probably benign |
Het |
Dnah11 |
A |
G |
12: 118,014,457 (GRCm39) |
I2010T |
probably damaging |
Het |
Dnhd1 |
A |
G |
7: 105,352,413 (GRCm39) |
Y2522C |
probably benign |
Het |
Dnhd1 |
T |
A |
7: 105,362,913 (GRCm39) |
I3825K |
possibly damaging |
Het |
Dst |
A |
T |
1: 34,238,452 (GRCm39) |
D3718V |
probably damaging |
Het |
Esp36 |
A |
G |
17: 38,730,330 (GRCm39) |
|
probably benign |
Het |
Fbxw21 |
T |
C |
9: 108,972,794 (GRCm39) |
Y380C |
probably damaging |
Het |
Fhad1 |
G |
A |
4: 141,649,634 (GRCm39) |
T836M |
probably damaging |
Het |
Fhod1 |
C |
T |
8: 106,074,463 (GRCm39) |
|
probably benign |
Het |
Flt1 |
A |
G |
5: 147,576,098 (GRCm39) |
C637R |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 53,008,436 (GRCm39) |
K809E |
probably damaging |
Het |
Grm1 |
G |
T |
10: 10,617,252 (GRCm39) |
Y510* |
probably null |
Het |
Hey1 |
A |
T |
3: 8,729,898 (GRCm39) |
H186Q |
possibly damaging |
Het |
Insyn1 |
C |
T |
9: 58,406,351 (GRCm39) |
A87V |
probably damaging |
Het |
Itga2b |
C |
T |
11: 102,350,963 (GRCm39) |
|
probably null |
Het |
Kcnv1 |
G |
A |
15: 44,977,840 (GRCm39) |
T66M |
probably damaging |
Het |
Lmcd1 |
A |
G |
6: 112,250,911 (GRCm39) |
D7G |
probably benign |
Het |
Lrrc1 |
T |
C |
9: 77,342,400 (GRCm39) |
D358G |
possibly damaging |
Het |
Lyn |
A |
G |
4: 3,748,765 (GRCm39) |
K248E |
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,045,990 (GRCm39) |
|
probably benign |
Het |
Map4k5 |
A |
T |
12: 69,891,187 (GRCm39) |
L160H |
probably damaging |
Het |
Mtcl2 |
T |
G |
2: 156,862,663 (GRCm39) |
H1422P |
probably damaging |
Het |
Myo6 |
C |
T |
9: 80,215,007 (GRCm39) |
R1247C |
probably damaging |
Het |
Myo9a |
A |
G |
9: 59,695,739 (GRCm39) |
E347G |
possibly damaging |
Het |
Ndfip1 |
C |
T |
18: 38,593,672 (GRCm39) |
P213S |
probably benign |
Het |
Neurl3 |
T |
C |
1: 36,308,470 (GRCm39) |
E114G |
possibly damaging |
Het |
Nlrp14 |
A |
T |
7: 106,795,370 (GRCm39) |
I877F |
probably benign |
Het |
Obscn |
A |
G |
11: 58,990,651 (GRCm39) |
S1733P |
probably benign |
Het |
Oxgr1 |
A |
T |
14: 120,260,185 (GRCm39) |
S7R |
probably benign |
Het |
Plcb1 |
A |
T |
2: 135,204,364 (GRCm39) |
|
probably benign |
Het |
Prkag2 |
G |
T |
5: 25,080,176 (GRCm39) |
N120K |
possibly damaging |
Het |
Rnf43 |
C |
T |
11: 87,622,485 (GRCm39) |
R529* |
probably null |
Het |
Saraf |
A |
G |
8: 34,632,442 (GRCm39) |
K174E |
possibly damaging |
Het |
Scrib |
T |
C |
15: 75,938,054 (GRCm39) |
Q264R |
probably benign |
Het |
Sh3rf3 |
T |
A |
10: 58,966,899 (GRCm39) |
M747K |
probably benign |
Het |
Shf |
T |
C |
2: 122,179,913 (GRCm39) |
H421R |
probably damaging |
Het |
Slc35g3 |
A |
G |
11: 69,651,368 (GRCm39) |
S228P |
probably damaging |
Het |
Slit1 |
A |
G |
19: 41,639,110 (GRCm39) |
|
probably benign |
Het |
Srrm4 |
A |
G |
5: 116,585,359 (GRCm39) |
|
probably benign |
Het |
Stfa1 |
T |
G |
16: 36,100,829 (GRCm39) |
V23G |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,872,498 (GRCm39) |
D371G |
probably benign |
Het |
Tada2a |
T |
C |
11: 83,993,926 (GRCm39) |
D186G |
probably damaging |
Het |
Tdpoz3 |
C |
A |
3: 93,733,618 (GRCm39) |
Q98K |
probably benign |
Het |
Tgfbrap1 |
A |
G |
1: 43,091,145 (GRCm39) |
V660A |
probably benign |
Het |
Tnn |
A |
G |
1: 159,945,978 (GRCm39) |
Y947H |
possibly damaging |
Het |
Vmn1r81 |
T |
A |
7: 11,994,441 (GRCm39) |
N56Y |
probably damaging |
Het |
Vsig8 |
A |
G |
1: 172,387,280 (GRCm39) |
D52G |
probably damaging |
Het |
Wdfy4 |
G |
A |
14: 32,764,469 (GRCm39) |
R2140C |
probably damaging |
Het |
|
Other mutations in Trim60 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Trim60
|
APN |
8 |
65,453,371 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03145:Trim60
|
APN |
8 |
65,453,224 (GRCm39) |
missense |
probably damaging |
0.99 |
R0054:Trim60
|
UTSW |
8 |
65,453,973 (GRCm39) |
missense |
probably benign |
0.05 |
R0054:Trim60
|
UTSW |
8 |
65,453,973 (GRCm39) |
missense |
probably benign |
0.05 |
R0080:Trim60
|
UTSW |
8 |
65,453,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R0244:Trim60
|
UTSW |
8 |
65,453,700 (GRCm39) |
missense |
probably benign |
0.07 |
R0348:Trim60
|
UTSW |
8 |
65,453,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Trim60
|
UTSW |
8 |
65,454,071 (GRCm39) |
missense |
probably benign |
0.04 |
R1667:Trim60
|
UTSW |
8 |
65,454,116 (GRCm39) |
missense |
probably benign |
0.00 |
R1944:Trim60
|
UTSW |
8 |
65,453,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2009:Trim60
|
UTSW |
8 |
65,453,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R4093:Trim60
|
UTSW |
8 |
65,454,030 (GRCm39) |
missense |
probably benign |
0.05 |
R4400:Trim60
|
UTSW |
8 |
65,453,864 (GRCm39) |
nonsense |
probably null |
|
R5171:Trim60
|
UTSW |
8 |
65,453,176 (GRCm39) |
missense |
probably benign |
0.05 |
R5898:Trim60
|
UTSW |
8 |
65,453,016 (GRCm39) |
nonsense |
probably null |
|
R6586:Trim60
|
UTSW |
8 |
65,453,248 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7012:Trim60
|
UTSW |
8 |
65,453,043 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7092:Trim60
|
UTSW |
8 |
65,453,700 (GRCm39) |
missense |
probably benign |
0.07 |
R7274:Trim60
|
UTSW |
8 |
65,453,133 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7567:Trim60
|
UTSW |
8 |
65,454,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R7761:Trim60
|
UTSW |
8 |
65,453,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9063:Trim60
|
UTSW |
8 |
65,453,465 (GRCm39) |
missense |
possibly damaging |
0.80 |
|