Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N01Rik |
A |
G |
10: 21,469,337 (GRCm39) |
D17G |
probably damaging |
Het |
Adam39 |
C |
T |
8: 41,277,695 (GRCm39) |
P29S |
probably benign |
Het |
Afap1l1 |
T |
C |
18: 61,874,880 (GRCm39) |
K434E |
possibly damaging |
Het |
Akap7 |
T |
C |
10: 25,115,565 (GRCm39) |
T187A |
probably damaging |
Het |
Atp7b |
A |
C |
8: 22,508,159 (GRCm39) |
I479S |
probably damaging |
Het |
Cdh23 |
T |
A |
10: 60,212,593 (GRCm39) |
E1606V |
probably damaging |
Het |
Cnga3 |
A |
G |
1: 37,300,755 (GRCm39) |
S530G |
probably damaging |
Het |
Col13a1 |
A |
G |
10: 61,727,040 (GRCm39) |
Y228H |
probably benign |
Het |
Cybb |
C |
A |
X: 9,319,892 (GRCm39) |
E203* |
probably null |
Het |
Dnah6 |
A |
T |
6: 73,018,037 (GRCm39) |
M3594K |
probably damaging |
Het |
Galnt14 |
C |
A |
17: 73,811,903 (GRCm39) |
Q439H |
possibly damaging |
Het |
Gck |
T |
A |
11: 5,859,093 (GRCm39) |
D158V |
probably damaging |
Het |
Gm5624 |
A |
G |
14: 44,798,222 (GRCm39) |
M85T |
possibly damaging |
Het |
Hgsnat |
A |
T |
8: 26,436,480 (GRCm39) |
N557K |
probably damaging |
Het |
Idua |
A |
G |
5: 108,829,362 (GRCm39) |
T388A |
probably benign |
Het |
Itgam |
A |
G |
7: 127,712,191 (GRCm39) |
D692G |
probably benign |
Het |
Lrrtm3 |
A |
G |
10: 63,924,799 (GRCm39) |
Y123H |
probably benign |
Het |
Mccc1 |
C |
T |
3: 36,022,595 (GRCm39) |
R566H |
probably benign |
Het |
Myh7 |
A |
T |
14: 55,220,802 (GRCm39) |
L999Q |
probably damaging |
Het |
Myo6 |
T |
G |
9: 80,207,947 (GRCm39) |
Y1146* |
probably null |
Het |
Nr3c1 |
C |
A |
18: 39,619,313 (GRCm39) |
G325W |
probably damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,434 (GRCm39) |
V173A |
probably benign |
Het |
Or5p72 |
T |
A |
7: 108,021,806 (GRCm39) |
H9Q |
probably benign |
Het |
Or7e170 |
T |
A |
9: 19,794,735 (GRCm39) |
I289F |
possibly damaging |
Het |
Phf1 |
T |
C |
17: 27,153,344 (GRCm39) |
|
probably null |
Het |
Piezo1 |
T |
C |
8: 123,209,660 (GRCm39) |
T2349A |
probably benign |
Het |
Pih1d1 |
T |
C |
7: 44,808,545 (GRCm39) |
|
probably null |
Het |
Pold3 |
A |
G |
7: 99,745,719 (GRCm39) |
S145P |
probably damaging |
Het |
Prpf38b |
G |
T |
3: 108,811,261 (GRCm39) |
|
probably benign |
Het |
Racgap1 |
A |
T |
15: 99,521,521 (GRCm39) |
M545K |
probably benign |
Het |
Safb |
T |
C |
17: 56,912,287 (GRCm39) |
Y802H |
probably damaging |
Het |
Serpina3f |
A |
T |
12: 104,183,716 (GRCm39) |
M193L |
probably benign |
Het |
Slc43a2 |
G |
A |
11: 75,459,263 (GRCm39) |
V432M |
probably benign |
Het |
Spata2l |
T |
C |
8: 123,960,075 (GRCm39) |
R405G |
possibly damaging |
Het |
Sv2c |
A |
G |
13: 96,125,606 (GRCm39) |
V377A |
probably damaging |
Het |
Tbc1d15 |
C |
T |
10: 115,038,421 (GRCm39) |
M597I |
probably benign |
Het |
Tenm4 |
A |
T |
7: 96,492,175 (GRCm39) |
R1036S |
probably damaging |
Het |
Tjp3 |
A |
G |
10: 81,119,522 (GRCm39) |
Y15H |
probably benign |
Het |
Tkt |
A |
G |
14: 30,282,645 (GRCm39) |
|
probably benign |
Het |
Tpm2 |
T |
C |
4: 43,519,447 (GRCm39) |
E145G |
probably damaging |
Het |
Trib2 |
G |
A |
12: 15,859,932 (GRCm39) |
H110Y |
probably damaging |
Het |
Ube2o |
T |
C |
11: 116,434,835 (GRCm39) |
E542G |
probably damaging |
Het |
Usp36 |
T |
C |
11: 118,170,067 (GRCm39) |
D218G |
probably damaging |
Het |
Zfp407 |
A |
G |
18: 84,227,846 (GRCm39) |
L1921P |
probably damaging |
Het |
Zfp983 |
G |
T |
17: 21,877,924 (GRCm39) |
M42I |
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 |
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 |
R1615:Trim60
|
UTSW |
8 |
65,453,162 (GRCm39) |
nonsense |
probably null |
|
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 |
|