Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd35 |
A |
T |
3: 96,591,460 (GRCm39) |
K582M |
probably benign |
Het |
Catsper3 |
T |
G |
13: 55,954,147 (GRCm39) |
V305G |
probably damaging |
Het |
Chd9 |
G |
A |
8: 91,683,198 (GRCm39) |
R546Q |
unknown |
Het |
Cnot6l |
G |
A |
5: 96,246,136 (GRCm39) |
T171I |
probably benign |
Het |
Cpne3 |
A |
G |
4: 19,535,292 (GRCm39) |
Y247H |
possibly damaging |
Het |
Cramp1 |
C |
G |
17: 25,232,884 (GRCm39) |
A39P |
probably damaging |
Het |
Cyp26b1 |
A |
T |
6: 84,554,035 (GRCm39) |
V194E |
probably benign |
Het |
Dchs1 |
A |
G |
7: 105,402,919 (GRCm39) |
S3208P |
probably benign |
Het |
Dhrs3 |
A |
G |
4: 144,653,755 (GRCm39) |
Y292C |
probably damaging |
Het |
Eif3l |
T |
C |
15: 78,968,412 (GRCm39) |
V227A |
probably damaging |
Het |
Eif4enif1 |
T |
C |
11: 3,174,716 (GRCm39) |
V290A |
probably damaging |
Het |
Epb41l4a |
A |
C |
18: 34,012,042 (GRCm39) |
Y159* |
probably null |
Het |
Gm5460 |
T |
A |
14: 33,739,326 (GRCm39) |
S103T |
|
Het |
Hpd |
G |
A |
5: 123,313,973 (GRCm39) |
T271M |
probably damaging |
Het |
Ift74 |
T |
C |
4: 94,506,271 (GRCm39) |
I18T |
probably benign |
Het |
Kif12 |
A |
G |
4: 63,087,704 (GRCm39) |
C260R |
probably damaging |
Het |
Klk15 |
C |
T |
7: 43,587,790 (GRCm39) |
H73Y |
possibly damaging |
Het |
Luc7l3 |
A |
G |
11: 94,188,676 (GRCm39) |
V201A |
unknown |
Het |
Mcrip2 |
T |
C |
17: 26,082,989 (GRCm39) |
E146G |
probably damaging |
Het |
Mctp1 |
T |
A |
13: 76,836,741 (GRCm39) |
Y323N |
probably benign |
Het |
Micu2 |
T |
A |
14: 58,156,363 (GRCm39) |
I370F |
probably damaging |
Het |
Mug2 |
T |
A |
6: 122,061,328 (GRCm39) |
V1416E |
probably damaging |
Het |
Mup3 |
T |
C |
4: 62,003,540 (GRCm39) |
N110D |
probably damaging |
Het |
Nav3 |
C |
T |
10: 109,699,613 (GRCm39) |
D294N |
possibly damaging |
Het |
Nphs2 |
G |
A |
1: 156,140,592 (GRCm39) |
A110T |
probably benign |
Het |
Or1a1 |
T |
C |
11: 74,086,563 (GRCm39) |
I78T |
possibly damaging |
Het |
Or5t7 |
A |
G |
2: 86,506,831 (GRCm39) |
M282T |
probably damaging |
Het |
Or6c215 |
G |
T |
10: 129,637,926 (GRCm39) |
P156Q |
probably damaging |
Het |
Otof |
C |
T |
5: 30,527,419 (GRCm39) |
|
probably null |
Het |
Pgrmc2 |
G |
T |
3: 41,037,105 (GRCm39) |
R109S |
probably benign |
Het |
Plb1 |
G |
A |
5: 32,439,079 (GRCm39) |
V214I |
probably damaging |
Het |
Ppp2r5d |
C |
T |
17: 46,998,906 (GRCm39) |
S52N |
probably benign |
Het |
Rrp12 |
C |
A |
19: 41,859,718 (GRCm39) |
E1082* |
probably null |
Het |
Skint3 |
A |
G |
4: 112,111,151 (GRCm39) |
E92G |
probably damaging |
Het |
Slc12a1 |
C |
G |
2: 124,996,004 (GRCm39) |
N52K |
probably benign |
Het |
Smu1 |
A |
G |
4: 40,738,361 (GRCm39) |
Y458H |
probably damaging |
Het |
Spsb3 |
C |
T |
17: 25,110,506 (GRCm39) |
P317S |
unknown |
Het |
Ssc5d |
A |
T |
7: 4,930,919 (GRCm39) |
Q167L |
probably damaging |
Het |
Ssh2 |
T |
C |
11: 77,328,454 (GRCm39) |
V340A |
probably damaging |
Het |
Stag3 |
G |
A |
5: 138,296,296 (GRCm39) |
R453H |
probably damaging |
Het |
Svil |
T |
A |
18: 5,056,239 (GRCm39) |
F371I |
probably benign |
Het |
Tas2r140 |
A |
C |
6: 133,032,181 (GRCm39) |
S192R |
possibly damaging |
Het |
Tdrp |
T |
C |
8: 14,003,840 (GRCm39) |
I166V |
possibly damaging |
Het |
Tgm3 |
C |
A |
2: 129,871,680 (GRCm39) |
Q269K |
probably benign |
Het |
Thsd7b |
G |
A |
1: 130,087,426 (GRCm39) |
C1181Y |
probably damaging |
Het |
Tinag |
A |
T |
9: 76,934,296 (GRCm39) |
|
probably benign |
Het |
Tnrc6b |
T |
C |
15: 80,763,179 (GRCm39) |
V227A |
possibly damaging |
Het |
Tox3 |
A |
C |
8: 90,996,864 (GRCm39) |
L133R |
possibly damaging |
Het |
Tshz1 |
A |
T |
18: 84,031,639 (GRCm39) |
I923N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,855,429 (GRCm39) |
V2498D |
probably damaging |
Het |
Vps41 |
T |
A |
13: 18,994,723 (GRCm39) |
|
probably null |
Het |
Xylt2 |
T |
C |
11: 94,555,462 (GRCm39) |
D850G |
probably damaging |
Het |
Zfp229 |
T |
A |
17: 21,964,321 (GRCm39) |
S184T |
possibly damaging |
Het |
Zfp518a |
G |
A |
19: 40,901,225 (GRCm39) |
V385I |
probably benign |
Het |
Zfp595 |
C |
A |
13: 67,468,989 (GRCm39) |
M12I |
probably benign |
Het |
Zfp750 |
T |
C |
11: 121,403,149 (GRCm39) |
Q533R |
probably benign |
Het |
|
Other mutations in Gsto1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00570:Gsto1
|
APN |
19 |
47,846,375 (GRCm39) |
missense |
probably benign |
0.24 |
R0277:Gsto1
|
UTSW |
19 |
47,846,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R1426:Gsto1
|
UTSW |
19 |
47,846,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R1733:Gsto1
|
UTSW |
19 |
47,843,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Gsto1
|
UTSW |
19 |
47,846,344 (GRCm39) |
missense |
probably benign |
0.01 |
R3419:Gsto1
|
UTSW |
19 |
47,846,344 (GRCm39) |
missense |
probably benign |
0.01 |
R3710:Gsto1
|
UTSW |
19 |
47,847,971 (GRCm39) |
critical splice donor site |
probably null |
|
R4830:Gsto1
|
UTSW |
19 |
47,852,830 (GRCm39) |
missense |
probably benign |
0.01 |
R4953:Gsto1
|
UTSW |
19 |
47,843,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5567:Gsto1
|
UTSW |
19 |
47,846,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5570:Gsto1
|
UTSW |
19 |
47,846,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6448:Gsto1
|
UTSW |
19 |
47,846,420 (GRCm39) |
missense |
probably benign |
0.02 |
R7994:Gsto1
|
UTSW |
19 |
47,847,899 (GRCm39) |
missense |
probably benign |
|
|