Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
T |
A |
8: 87,235,770 (GRCm39) |
D1199V |
probably damaging |
Het |
Abcc6 |
A |
T |
7: 45,664,999 (GRCm39) |
S277R |
probably benign |
Het |
Acvrl1 |
A |
G |
15: 101,035,280 (GRCm39) |
S269G |
probably damaging |
Het |
Akap10 |
T |
C |
11: 61,806,048 (GRCm39) |
S227G |
probably benign |
Het |
Angptl8 |
T |
C |
9: 21,747,112 (GRCm39) |
|
probably null |
Het |
Arsi |
T |
C |
18: 61,049,539 (GRCm39) |
S141P |
possibly damaging |
Het |
Atic |
T |
A |
1: 71,608,216 (GRCm39) |
Y303* |
probably null |
Het |
Bbs9 |
C |
T |
9: 22,557,359 (GRCm39) |
P510L |
probably benign |
Het |
Bcl2a1b |
A |
G |
9: 89,081,795 (GRCm39) |
N128S |
probably benign |
Het |
Bcl2a1d |
A |
T |
9: 88,613,549 (GRCm39) |
M75K |
probably damaging |
Het |
Carm1 |
T |
A |
9: 21,494,836 (GRCm39) |
L324Q |
probably damaging |
Het |
Caskin1 |
T |
A |
17: 24,722,782 (GRCm39) |
L550Q |
probably damaging |
Het |
Cd302 |
A |
G |
2: 60,087,412 (GRCm39) |
I142T |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,738,882 (GRCm39) |
D2320E |
probably benign |
Het |
Cgnl1 |
A |
G |
9: 71,632,461 (GRCm39) |
S297P |
probably damaging |
Het |
Cr1l |
T |
A |
1: 194,789,210 (GRCm39) |
Y398F |
probably benign |
Het |
Ctsa |
A |
T |
2: 164,676,813 (GRCm39) |
D145V |
probably benign |
Het |
Ctsj |
C |
T |
13: 61,148,388 (GRCm39) |
G303D |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,016,800 (GRCm39) |
I250M |
probably benign |
Het |
Doc2a |
C |
A |
7: 126,447,919 (GRCm39) |
C54* |
probably null |
Het |
Dpy19l2 |
T |
C |
9: 24,492,544 (GRCm39) |
T685A |
probably damaging |
Het |
Dtna |
T |
A |
18: 23,728,535 (GRCm39) |
C243* |
probably null |
Het |
Exoc3l4 |
A |
G |
12: 111,388,690 (GRCm39) |
T60A |
possibly damaging |
Het |
Exph5 |
C |
A |
9: 53,286,225 (GRCm39) |
S1102* |
probably null |
Het |
Fhl3 |
T |
C |
4: 124,599,481 (GRCm39) |
Y19H |
probably damaging |
Het |
Flt4 |
A |
G |
11: 49,528,646 (GRCm39) |
E1012G |
possibly damaging |
Het |
Flvcr2 |
A |
G |
12: 85,829,777 (GRCm39) |
N262S |
probably benign |
Het |
Gon4l |
G |
T |
3: 88,766,350 (GRCm39) |
C463F |
probably damaging |
Het |
H2-T10 |
A |
T |
17: 36,428,631 (GRCm39) |
|
probably null |
Het |
Heatr3 |
T |
C |
8: 88,871,200 (GRCm39) |
C185R |
probably benign |
Het |
Hectd1 |
A |
G |
12: 51,792,317 (GRCm39) |
V2474A |
probably benign |
Het |
Htr3a |
C |
T |
9: 48,812,795 (GRCm39) |
E215K |
probably damaging |
Het |
Ica1l |
T |
C |
1: 60,045,451 (GRCm39) |
T271A |
probably benign |
Het |
Klra2 |
A |
G |
6: 131,220,864 (GRCm39) |
I66T |
probably benign |
Het |
Neto2 |
T |
C |
8: 86,417,541 (GRCm39) |
K21R |
probably benign |
Het |
Niban1 |
A |
G |
1: 151,565,365 (GRCm39) |
T232A |
probably benign |
Het |
Nisch |
T |
A |
14: 30,906,971 (GRCm39) |
|
probably benign |
Het |
Nr4a1 |
G |
T |
15: 101,169,618 (GRCm39) |
R296L |
probably damaging |
Het |
Obscn |
T |
C |
11: 59,022,472 (GRCm39) |
R758G |
possibly damaging |
Het |
Or7g19 |
T |
A |
9: 18,856,496 (GRCm39) |
I184N |
probably damaging |
Het |
Or8b50 |
T |
C |
9: 38,518,397 (GRCm39) |
V212A |
probably benign |
Het |
Pcsk5 |
A |
T |
19: 17,452,198 (GRCm39) |
C1102* |
probably null |
Het |
Phip |
C |
T |
9: 82,757,358 (GRCm39) |
A1605T |
probably benign |
Het |
Pstpip2 |
T |
A |
18: 77,942,564 (GRCm39) |
M105K |
possibly damaging |
Het |
Qprt |
C |
T |
7: 126,707,532 (GRCm39) |
V219I |
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,195,112 (GRCm39) |
N1271K |
probably damaging |
Het |
Reg3g |
A |
T |
6: 78,444,475 (GRCm39) |
L106H |
probably damaging |
Het |
Rhobtb1 |
G |
A |
10: 69,106,254 (GRCm39) |
G273D |
probably benign |
Het |
Rimbp2 |
T |
C |
5: 128,861,952 (GRCm39) |
D771G |
probably damaging |
Het |
Sos2 |
T |
C |
12: 69,643,573 (GRCm39) |
I935V |
possibly damaging |
Het |
Tcf12 |
A |
T |
9: 71,763,792 (GRCm39) |
N397K |
probably damaging |
Het |
Tgtp2 |
T |
C |
11: 48,949,957 (GRCm39) |
Q205R |
probably benign |
Het |
Tle5 |
T |
A |
10: 81,400,712 (GRCm39) |
C89S |
possibly damaging |
Het |
Unc13b |
A |
G |
4: 43,095,843 (GRCm39) |
T84A |
probably benign |
Het |
Usb1 |
T |
A |
8: 96,069,759 (GRCm39) |
F102L |
probably benign |
Het |
Vmn2r61 |
A |
G |
7: 41,949,529 (GRCm39) |
T650A |
possibly damaging |
Het |
Zbtb41 |
A |
C |
1: 139,350,923 (GRCm39) |
D12A |
probably benign |
Het |
Zbtb41 |
G |
T |
1: 139,350,925 (GRCm39) |
E13* |
probably null |
Het |
Zfp821 |
C |
T |
8: 110,447,872 (GRCm39) |
S71F |
probably damaging |
Het |
|
Other mutations in Tubb2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00499:Tubb2b
|
APN |
13 |
34,312,329 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00575:Tubb2b
|
APN |
13 |
34,313,244 (GRCm39) |
missense |
probably damaging |
0.99 |
R1246:Tubb2b
|
UTSW |
13 |
34,312,130 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2055:Tubb2b
|
UTSW |
13 |
34,311,708 (GRCm39) |
missense |
probably benign |
0.02 |
R2071:Tubb2b
|
UTSW |
13 |
34,312,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Tubb2b
|
UTSW |
13 |
34,314,198 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4905:Tubb2b
|
UTSW |
13 |
34,312,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Tubb2b
|
UTSW |
13 |
34,312,168 (GRCm39) |
nonsense |
probably null |
|
R5635:Tubb2b
|
UTSW |
13 |
34,312,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6349:Tubb2b
|
UTSW |
13 |
34,311,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Tubb2b
|
UTSW |
13 |
34,311,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R6994:Tubb2b
|
UTSW |
13 |
34,311,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Tubb2b
|
UTSW |
13 |
34,312,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R8936:Tubb2b
|
UTSW |
13 |
34,312,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Tubb2b
|
UTSW |
13 |
34,311,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Tubb2b
|
UTSW |
13 |
34,311,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R9787:Tubb2b
|
UTSW |
13 |
34,312,409 (GRCm39) |
missense |
probably benign |
0.41 |
|