Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700010I14Rik |
T |
A |
17: 9,226,935 (GRCm39) |
C497S |
probably benign |
Het |
4930453N24Rik |
A |
T |
16: 64,589,377 (GRCm39) |
Y92* |
probably null |
Het |
Adam3 |
A |
G |
8: 25,205,127 (GRCm39) |
V117A |
probably benign |
Het |
Amer2 |
G |
C |
14: 60,617,376 (GRCm39) |
D524H |
probably damaging |
Het |
Armh4 |
T |
A |
14: 50,011,695 (GRCm39) |
D4V |
probably damaging |
Het |
Atp6v0a4 |
T |
C |
6: 38,029,988 (GRCm39) |
K692R |
probably benign |
Het |
Atp8b1 |
A |
G |
18: 64,684,931 (GRCm39) |
V730A |
probably benign |
Het |
Bdh2 |
T |
C |
3: 134,991,309 (GRCm39) |
|
probably benign |
Het |
Ccnd3 |
T |
A |
17: 47,905,332 (GRCm39) |
|
probably null |
Het |
Chrm4 |
T |
C |
2: 91,758,075 (GRCm39) |
V161A |
possibly damaging |
Het |
Csmd3 |
T |
C |
15: 47,751,892 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,087,930 (GRCm39) |
S349P |
probably benign |
Het |
Ddx55 |
A |
G |
5: 124,697,370 (GRCm39) |
N244S |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,500,825 (GRCm39) |
|
probably benign |
Het |
Dppa3 |
T |
C |
6: 122,605,724 (GRCm39) |
S93P |
probably damaging |
Het |
Echdc1 |
T |
C |
10: 29,220,426 (GRCm39) |
I217T |
probably damaging |
Het |
Fpr-rs4 |
T |
A |
17: 18,242,416 (GRCm39) |
L141Q |
probably damaging |
Het |
Galnt15 |
T |
C |
14: 31,771,935 (GRCm39) |
F451L |
probably damaging |
Het |
Galnt9 |
G |
A |
5: 110,692,665 (GRCm39) |
R33H |
probably benign |
Het |
Iah1 |
G |
A |
12: 21,367,402 (GRCm39) |
G36D |
probably damaging |
Het |
Jakmip1 |
A |
G |
5: 37,332,857 (GRCm39) |
D1179G |
probably benign |
Het |
Kcnh1 |
A |
G |
1: 192,188,055 (GRCm39) |
T866A |
probably benign |
Het |
Kcnq4 |
T |
A |
4: 120,555,150 (GRCm39) |
I678F |
probably benign |
Het |
Lman2 |
T |
C |
13: 55,500,773 (GRCm39) |
D142G |
probably damaging |
Het |
Lrp1b |
T |
C |
2: 40,587,564 (GRCm39) |
D3897G |
|
Het |
Lrrn1 |
T |
A |
6: 107,544,820 (GRCm39) |
I206N |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,850,143 (GRCm39) |
L802H |
probably damaging |
Het |
Meaf6 |
T |
C |
4: 125,001,450 (GRCm39) |
|
probably benign |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Mis18bp1 |
G |
A |
12: 65,180,616 (GRCm39) |
S955L |
probably benign |
Het |
Mocs1 |
T |
A |
17: 49,756,819 (GRCm39) |
M267K |
probably damaging |
Het |
Mroh3 |
T |
A |
1: 136,128,110 (GRCm39) |
Y263F |
probably damaging |
Het |
Ndufs1 |
A |
T |
1: 63,198,878 (GRCm39) |
|
probably benign |
Het |
Nuak1 |
T |
C |
10: 84,210,492 (GRCm39) |
Y532C |
probably damaging |
Het |
Or51b6 |
A |
G |
7: 103,556,165 (GRCm39) |
H170R |
|
Het |
Or6c205 |
A |
T |
10: 129,086,669 (GRCm39) |
T89S |
possibly damaging |
Het |
Ost4 |
A |
G |
5: 31,064,866 (GRCm39) |
V5A |
possibly damaging |
Het |
P2rx1 |
T |
A |
11: 72,900,059 (GRCm39) |
C159S |
probably damaging |
Het |
Paqr8 |
T |
C |
1: 21,005,614 (GRCm39) |
L256P |
possibly damaging |
Het |
Pgls |
T |
A |
8: 72,048,689 (GRCm39) |
|
probably benign |
Het |
Pkd2l1 |
T |
C |
19: 44,140,864 (GRCm39) |
E566G |
possibly damaging |
Het |
Plau |
A |
T |
14: 20,889,613 (GRCm39) |
H226L |
probably damaging |
Het |
Rps18-ps5 |
A |
G |
13: 28,441,872 (GRCm39) |
N85S |
probably damaging |
Het |
Rraga |
T |
C |
4: 86,494,675 (GRCm39) |
S174P |
probably damaging |
Het |
Sacs |
T |
A |
14: 61,445,185 (GRCm39) |
D2410E |
probably benign |
Het |
Sgms1 |
A |
T |
19: 32,137,227 (GRCm39) |
M113K |
probably benign |
Het |
Skint6 |
C |
A |
4: 113,095,347 (GRCm39) |
G104V |
probably damaging |
Het |
Spata31f1e |
C |
T |
4: 42,792,546 (GRCm39) |
G529S |
probably benign |
Het |
Sqor |
T |
A |
2: 122,649,876 (GRCm39) |
Y373* |
probably null |
Het |
Stra6l |
T |
A |
4: 45,864,910 (GRCm39) |
S79T |
possibly damaging |
Het |
Svep1 |
T |
C |
4: 58,091,915 (GRCm39) |
I1573M |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,146,224 (GRCm39) |
D1674G |
possibly damaging |
Het |
Tex26 |
C |
A |
5: 149,376,884 (GRCm39) |
T91N |
probably damaging |
Het |
Tigd2 |
T |
G |
6: 59,187,887 (GRCm39) |
S251R |
probably damaging |
Het |
Tmco1 |
C |
T |
1: 167,136,132 (GRCm39) |
|
probably benign |
Het |
Tnks1bp1 |
T |
A |
2: 84,901,048 (GRCm39) |
L1585Q |
probably damaging |
Het |
Trmt10c |
A |
G |
16: 55,855,542 (GRCm39) |
V31A |
probably benign |
Het |
Ttc41 |
T |
C |
10: 86,569,625 (GRCm39) |
S668P |
probably damaging |
Het |
Uggt2 |
A |
T |
14: 119,326,724 (GRCm39) |
D162E |
probably damaging |
Het |
Vmn1r125 |
G |
C |
7: 21,006,503 (GRCm39) |
V134L |
probably benign |
Het |
Vmn1r225 |
T |
A |
17: 20,723,449 (GRCm39) |
F297I |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,845,006 (GRCm39) |
D2030G |
probably benign |
Het |
|
Other mutations in Lars2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01743:Lars2
|
APN |
9 |
123,282,313 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01993:Lars2
|
APN |
9 |
123,224,008 (GRCm39) |
splice site |
probably benign |
|
IGL02155:Lars2
|
APN |
9 |
123,284,047 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02941:Lars2
|
APN |
9 |
123,288,650 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03090:Lars2
|
APN |
9 |
123,285,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03271:Lars2
|
APN |
9 |
123,288,549 (GRCm39) |
splice site |
probably null |
|
IGL03386:Lars2
|
APN |
9 |
123,282,455 (GRCm39) |
nonsense |
probably null |
|
IGL03410:Lars2
|
APN |
9 |
123,247,841 (GRCm39) |
missense |
possibly damaging |
0.87 |
ulrich
|
UTSW |
9 |
123,247,758 (GRCm39) |
missense |
probably damaging |
0.99 |
K3955:Lars2
|
UTSW |
9 |
123,206,842 (GRCm39) |
missense |
probably damaging |
1.00 |
P0038:Lars2
|
UTSW |
9 |
123,206,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Lars2
|
UTSW |
9 |
123,267,186 (GRCm39) |
splice site |
probably benign |
|
R1671:Lars2
|
UTSW |
9 |
123,247,344 (GRCm39) |
missense |
probably benign |
0.02 |
R1829:Lars2
|
UTSW |
9 |
123,260,982 (GRCm39) |
missense |
probably benign |
0.00 |
R2219:Lars2
|
UTSW |
9 |
123,247,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R2220:Lars2
|
UTSW |
9 |
123,247,845 (GRCm39) |
missense |
probably damaging |
0.98 |
R4610:Lars2
|
UTSW |
9 |
123,247,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R5027:Lars2
|
UTSW |
9 |
123,270,560 (GRCm39) |
missense |
probably benign |
0.38 |
R5195:Lars2
|
UTSW |
9 |
123,282,375 (GRCm39) |
missense |
probably damaging |
0.97 |
R5597:Lars2
|
UTSW |
9 |
123,284,047 (GRCm39) |
missense |
probably damaging |
0.99 |
R5756:Lars2
|
UTSW |
9 |
123,267,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R5783:Lars2
|
UTSW |
9 |
123,290,661 (GRCm39) |
missense |
probably benign |
|
R6045:Lars2
|
UTSW |
9 |
123,201,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Lars2
|
UTSW |
9 |
123,240,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R6323:Lars2
|
UTSW |
9 |
123,270,659 (GRCm39) |
nonsense |
probably null |
|
R6377:Lars2
|
UTSW |
9 |
123,283,825 (GRCm39) |
missense |
probably benign |
0.00 |
R6395:Lars2
|
UTSW |
9 |
123,200,990 (GRCm39) |
missense |
probably benign |
0.06 |
R7094:Lars2
|
UTSW |
9 |
123,288,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R7144:Lars2
|
UTSW |
9 |
123,261,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R7233:Lars2
|
UTSW |
9 |
123,241,019 (GRCm39) |
nonsense |
probably null |
|
R7254:Lars2
|
UTSW |
9 |
123,284,028 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7350:Lars2
|
UTSW |
9 |
123,256,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R7413:Lars2
|
UTSW |
9 |
123,288,568 (GRCm39) |
missense |
probably benign |
0.30 |
R7614:Lars2
|
UTSW |
9 |
123,224,176 (GRCm39) |
missense |
|
|
R7683:Lars2
|
UTSW |
9 |
123,206,895 (GRCm39) |
critical splice donor site |
probably null |
|
R8000:Lars2
|
UTSW |
9 |
123,265,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Lars2
|
UTSW |
9 |
123,288,562 (GRCm39) |
missense |
probably benign |
|
R8355:Lars2
|
UTSW |
9 |
123,283,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R8364:Lars2
|
UTSW |
9 |
123,241,019 (GRCm39) |
nonsense |
probably null |
|
R8818:Lars2
|
UTSW |
9 |
123,221,892 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9351:Lars2
|
UTSW |
9 |
123,265,366 (GRCm39) |
missense |
probably benign |
0.38 |
Z1177:Lars2
|
UTSW |
9 |
123,283,847 (GRCm39) |
missense |
probably damaging |
1.00 |
|