Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atp13a5 |
G |
A |
16: 29,167,833 (GRCm39) |
P109S |
probably benign |
Het |
Baiap2l1 |
T |
C |
5: 144,222,916 (GRCm39) |
K106R |
probably benign |
Het |
Coro6 |
A |
G |
11: 77,357,030 (GRCm39) |
I111V |
possibly damaging |
Het |
Crocc2 |
A |
G |
1: 93,118,223 (GRCm39) |
E382G |
probably benign |
Het |
Dhrs7l |
A |
T |
12: 72,668,724 (GRCm39) |
N44K |
possibly damaging |
Het |
Dnah5 |
C |
A |
15: 28,409,266 (GRCm39) |
N3561K |
probably benign |
Het |
Dsc2 |
T |
A |
18: 20,165,335 (GRCm39) |
E879D |
probably benign |
Het |
Frk |
A |
G |
10: 34,481,835 (GRCm39) |
Y375C |
probably benign |
Het |
Herc2 |
A |
T |
7: 55,717,840 (GRCm39) |
R61* |
probably null |
Het |
Jarid2 |
A |
G |
13: 45,027,872 (GRCm39) |
D146G |
probably damaging |
Het |
Lancl2 |
C |
A |
6: 57,699,566 (GRCm39) |
T127K |
probably damaging |
Het |
Large1 |
G |
A |
8: 73,609,892 (GRCm39) |
Q359* |
probably null |
Het |
Mast2 |
C |
A |
4: 116,173,694 (GRCm39) |
E521* |
probably null |
Het |
Mrc1 |
T |
A |
2: 14,299,597 (GRCm39) |
|
probably null |
Het |
Obi1 |
T |
C |
14: 104,759,993 (GRCm39) |
H19R |
possibly damaging |
Het |
Or4z4 |
A |
G |
19: 12,076,727 (GRCm39) |
I92T |
probably damaging |
Het |
Or5ak23 |
T |
C |
2: 85,244,425 (GRCm39) |
N266S |
probably benign |
Het |
Or6c38 |
A |
T |
10: 128,929,323 (GRCm39) |
D173E |
possibly damaging |
Het |
Or8k38 |
T |
C |
2: 86,488,406 (GRCm39) |
Y132C |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
P2ry14 |
T |
C |
3: 59,023,154 (GRCm39) |
Y102C |
probably damaging |
Het |
Pcdhga6 |
T |
A |
18: 37,842,702 (GRCm39) |
D807E |
probably benign |
Het |
Pcdhgb4 |
T |
A |
18: 37,854,737 (GRCm39) |
N377K |
probably damaging |
Het |
Phf13 |
T |
A |
4: 152,076,114 (GRCm39) |
N263Y |
probably damaging |
Het |
Rab19 |
T |
A |
6: 39,365,060 (GRCm39) |
S107T |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,165,027 (GRCm39) |
F380I |
probably damaging |
Het |
Reep1 |
T |
C |
6: 71,784,826 (GRCm39) |
|
probably benign |
Het |
Rpgrip1l |
C |
T |
8: 91,959,499 (GRCm39) |
E1134K |
possibly damaging |
Het |
Serpina3m |
A |
T |
12: 104,357,766 (GRCm39) |
Y230F |
probably benign |
Het |
Skint3 |
T |
C |
4: 112,111,061 (GRCm39) |
I62T |
probably damaging |
Het |
Smg6 |
T |
C |
11: 74,823,279 (GRCm39) |
|
probably null |
Het |
Sp4 |
G |
A |
12: 118,263,077 (GRCm39) |
T323I |
possibly damaging |
Het |
Tepsin |
C |
T |
11: 119,986,428 (GRCm39) |
G128D |
probably benign |
Het |
Togaram2 |
A |
G |
17: 71,996,266 (GRCm39) |
N89D |
probably damaging |
Het |
Trim36 |
T |
C |
18: 46,321,475 (GRCm39) |
T191A |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,077,980 (GRCm39) |
|
probably null |
Het |
Zfp418 |
G |
A |
7: 7,184,895 (GRCm39) |
C286Y |
probably damaging |
Het |
|
Other mutations in Strc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01102:Strc
|
APN |
2 |
121,195,541 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01152:Strc
|
APN |
2 |
121,201,276 (GRCm39) |
missense |
probably benign |
|
IGL01608:Strc
|
APN |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01695:Strc
|
APN |
2 |
121,205,779 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01715:Strc
|
APN |
2 |
121,196,218 (GRCm39) |
splice site |
probably null |
|
IGL01906:Strc
|
APN |
2 |
121,208,115 (GRCm39) |
missense |
probably benign |
|
IGL02135:Strc
|
APN |
2 |
121,195,315 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02416:Strc
|
APN |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02455:Strc
|
APN |
2 |
121,206,272 (GRCm39) |
unclassified |
probably benign |
|
IGL03029:Strc
|
APN |
2 |
121,194,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03176:Strc
|
APN |
2 |
121,202,661 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Strc
|
APN |
2 |
121,202,232 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Strc
|
UTSW |
2 |
121,204,161 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02799:Strc
|
UTSW |
2 |
121,209,717 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4283001:Strc
|
UTSW |
2 |
121,205,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Strc
|
UTSW |
2 |
121,198,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Strc
|
UTSW |
2 |
121,210,014 (GRCm39) |
missense |
probably damaging |
0.99 |
R1065:Strc
|
UTSW |
2 |
121,197,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1148:Strc
|
UTSW |
2 |
121,202,558 (GRCm39) |
intron |
probably benign |
|
R1203:Strc
|
UTSW |
2 |
121,202,604 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1343:Strc
|
UTSW |
2 |
121,195,596 (GRCm39) |
missense |
probably benign |
0.21 |
R1544:Strc
|
UTSW |
2 |
121,203,219 (GRCm39) |
splice site |
probably null |
|
R1650:Strc
|
UTSW |
2 |
121,211,366 (GRCm39) |
start gained |
probably benign |
|
R1840:Strc
|
UTSW |
2 |
121,209,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Strc
|
UTSW |
2 |
121,201,518 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2035:Strc
|
UTSW |
2 |
121,205,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Strc
|
UTSW |
2 |
121,209,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Strc
|
UTSW |
2 |
121,196,343 (GRCm39) |
missense |
probably benign |
0.10 |
R2219:Strc
|
UTSW |
2 |
121,195,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Strc
|
UTSW |
2 |
121,195,592 (GRCm39) |
missense |
probably damaging |
0.99 |
R4375:Strc
|
UTSW |
2 |
121,211,304 (GRCm39) |
missense |
unknown |
|
R4563:Strc
|
UTSW |
2 |
121,196,286 (GRCm39) |
missense |
probably benign |
0.02 |
R4578:Strc
|
UTSW |
2 |
121,208,484 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4607:Strc
|
UTSW |
2 |
121,203,426 (GRCm39) |
missense |
probably benign |
0.31 |
R4651:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4652:Strc
|
UTSW |
2 |
121,204,829 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4790:Strc
|
UTSW |
2 |
121,206,075 (GRCm39) |
missense |
probably benign |
0.05 |
R5480:Strc
|
UTSW |
2 |
121,195,300 (GRCm39) |
missense |
probably benign |
0.00 |
R5580:Strc
|
UTSW |
2 |
121,205,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R5679:Strc
|
UTSW |
2 |
121,198,581 (GRCm39) |
missense |
probably benign |
0.03 |
R5703:Strc
|
UTSW |
2 |
121,201,295 (GRCm39) |
missense |
probably benign |
|
R5841:Strc
|
UTSW |
2 |
121,196,358 (GRCm39) |
missense |
probably benign |
0.29 |
R5917:Strc
|
UTSW |
2 |
121,209,790 (GRCm39) |
missense |
probably benign |
|
R5958:Strc
|
UTSW |
2 |
121,207,403 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6320:Strc
|
UTSW |
2 |
121,205,439 (GRCm39) |
missense |
probably benign |
0.16 |
R6695:Strc
|
UTSW |
2 |
121,207,705 (GRCm39) |
missense |
probably benign |
0.35 |
R6970:Strc
|
UTSW |
2 |
121,208,495 (GRCm39) |
missense |
probably benign |
0.41 |
R7018:Strc
|
UTSW |
2 |
121,199,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7045:Strc
|
UTSW |
2 |
121,201,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R7190:Strc
|
UTSW |
2 |
121,199,507 (GRCm39) |
missense |
probably benign |
0.14 |
R7283:Strc
|
UTSW |
2 |
121,209,933 (GRCm39) |
missense |
probably damaging |
0.99 |
R7694:Strc
|
UTSW |
2 |
121,207,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7700:Strc
|
UTSW |
2 |
121,202,229 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7756:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7758:Strc
|
UTSW |
2 |
121,201,427 (GRCm39) |
missense |
probably benign |
|
R7822:Strc
|
UTSW |
2 |
121,208,219 (GRCm39) |
missense |
probably benign |
0.01 |
R7830:Strc
|
UTSW |
2 |
121,205,530 (GRCm39) |
missense |
probably damaging |
0.99 |
R7953:Strc
|
UTSW |
2 |
121,207,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R8137:Strc
|
UTSW |
2 |
121,197,219 (GRCm39) |
missense |
probably damaging |
0.98 |
R8394:Strc
|
UTSW |
2 |
121,209,490 (GRCm39) |
missense |
probably benign |
0.00 |
R8427:Strc
|
UTSW |
2 |
121,208,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R8792:Strc
|
UTSW |
2 |
121,208,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R8874:Strc
|
UTSW |
2 |
121,205,353 (GRCm39) |
critical splice donor site |
probably null |
|
R8947:Strc
|
UTSW |
2 |
121,201,470 (GRCm39) |
missense |
probably benign |
0.09 |
R9285:Strc
|
UTSW |
2 |
121,195,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9302:Strc
|
UTSW |
2 |
121,211,336 (GRCm39) |
missense |
unknown |
|
R9386:Strc
|
UTSW |
2 |
121,198,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R9438:Strc
|
UTSW |
2 |
121,198,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R9581:Strc
|
UTSW |
2 |
121,207,928 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Strc
|
UTSW |
2 |
121,209,525 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Strc
|
UTSW |
2 |
121,206,002 (GRCm39) |
missense |
probably damaging |
0.98 |
|